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Telephone-delivered Mindfulness Intervention for African American Dementia Caregivers

Easing the Burden of Dementia Caregiving: A Telephone-delivered Mindfulness Intervention for Rural, African American Families

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04058886
Enrollment
57
Registered
2019-08-16
Start date
2019-11-15
Completion date
2022-07-06
Last updated
2023-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Dementia, Caregiver, Dementia Alzheimers

Brief summary

This study is assesses the feasibility and acceptability of telephone-delivered mindfulness training designed to alleviate caregiver burden for African-American rural caregivers of individuals with moderate to severe dementia, as defined by the caregiver. The study utilizes a single-group, uncontrolled design to test the feasibility and acceptability of the intervention for the target population.

Detailed description

Mindfulness interventions can decrease caregiver burden and improve coping skills, including decreased emotion-based coping, increased tolerance for uncertainty, improved psychological well-being and quality of life while potentially improving relationship quality and communication. This study utilizes a single-group, uncontrolled design to assess the feasibility and acceptability of telephone-delivered mindfulness training designed to alleviate caregiver burden for African-American rural caregivers of individuals with moderate to severe dementia, as defined by the caregiver. The telephone-delivered mindfulness intervention will improve geographical access for rural caregivers and deem more flexible for a caregiver's schedule. The study's intervention consists of mindfulness training delivered by telephone once weekly for 8 weeks. The intervention also includes one retreat for which respite care will be provided, if needed. The intervention, based on, Kabat-Zinn's mindfulness-based stress reduction (MBSR), will emphasize the following: 1) mindful experiencing, including mindfulness of feelings and body sensations; 2) mindful communication, including non-verbal mindfulness, mindful listening, and mindful speaking; and 3) mindful compassion for self and others.

Interventions

BEHAVIORALTelephone-delivered Mindfulness

The telephone-delivered mindfulness training intervention that will incorporate the following elements: 1) training for primary caregivers (CG) and their caregiving partner (CP) in a telephone-based mindfulness training intervention; 2) groups of up to eight participants (four CG-CP pairs) plus an instructor, on a shared telephone line; and 3) training in a 8-week, modified MBSR program, which places additional emphasis on training in the following: a) mindful experiencing, including mindfulness of feelings and body sensations; b) mindful communication, including non-verbal mindfulness, mindful listening, and mindful speaking; and c) mindful compassion for self and others. Additionally, homework assignments will involve listening to exercises on a dial-in telephone line; and assignments for CG-CP dyads (e.g. mindful listening and communication practices) as well as CG mindfulness practices in the presence of care recipients (e.g. mindful eating, and mindful listening).

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* The candidate is at least 18 years old; * The candidate self-identifies as Black or African American; * The candidate provides at least 4 hours of care per day to the care recipient, who must have either a diagnosis of dementia OR have a score of at least 2 or higher on the Alzheimer's Disease Screening tool (AD-8) or a score of 8 or higher on the Functional Assessment Staging of Alzheimer's disease (FAST) scale (indicative of moderate - severe dementia); * The candidate is able to identify and recruit an additional informal caregiver (care partner) to participate in the study. The care partner must consider themselves as part of the caregiving team that helps to make decisions about the care of the care recipient. The care partner may be a blood relative or close friend, but not a formal caregiver. The care partner need not live in the same geographic area. * Both the candidate primary caregiver and care partner must have access to a telephone and express a willingness to participate in the pre- and post-participation assessments, the intervention calls, and the intervention retreat.

Exclusion criteria

* The candidate is too unwell to participate; e.g., with an active diagnosis of cancer or more than 3 hospitalizations in the past year; * The primary caregiver is unable to identify and recruit a care partner willing to commit to the study requirements; * The care recipient does not meet the criteria for dementia.

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Attending at Least 6 Telephone Sessions8 weeksThe instructor will conduct a role call to take attendance at the beginning of each of the 8 class sessions and 1 retreat session. Eighty-five percent of participants who start the intervention will complete at least 6 out of 9 intervention sessions. Attendance used as a proxy to assess intervention acceptability.
Percent of Dyads Who Endorse the Program8 weeksThe intervention will be acceptable to informal caregiving teams as evidenced by an 85 percent (95% Confidence Interval (CI): 72.5, 97.5) endorsement of the program in post-participation interviews. Calculated based on responses to open-ended questions regarding participants' experiences of the intervention. Examples of questions are: how valuable or beneficial was the mindfulness training to you? and what challenges did you have with the training? and what did you expect from the training that you did not get?. Endorsement was considered positive if the expressions of value outweighed challenges (i.e., positive comments outweighed negative comments by dyad). Data reported as caregiving teams (dyads) in accordance with the protocol.

Secondary

MeasureTime frameDescription
Change From Baseline in Intolerance of Uncertainty Scale (IUS-12) Prospective Subscale Scoreup to 8 weeksThe prospective anxiety subscale of the Intolerance of Uncertainty Scale (IUS-12) is a 7-item measure. The measure uses a 5-point Likert scale (1=not at all like me to 5=entirely like me). Scores range from 7-35, with lower scores reflecting more tolerance of uncertain situations. IUS-12 was administered at Baseline and at 8 weeks. Change scores are reported from paired t-tests for within-group assessments and from mixed effects models for the total population controlling for caregiving role, severity of dementia in the care recipient and dependencies in the data (individuals within families within cohorts).
Change From Baseline in Intolerance of Uncertainty Scale (IUS-12) Inhibitory Subscale Scoreup to 8 weeksThe inhibitory subscale of the Intolerance of Uncertainty Scale (IUS-12) is a 5-item measure. The measure uses a 5-point Likert scale (1=not at all like me to 5=entirely like me). Total scores range from 5-25, with lower scores reflecting more tolerance of uncertain situations. IUS-12 was administered at baseline and at 8 weeks. Within group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Meaning and Purpose-Short Form 6aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Meaning and Purpose-Short Form 6a is a 6-item scale that assesses a sense that life has purpose and there are good reasons for living, including hopefulness, optimism, goal-directedness, and feelings that one's life is worthy. It uses a 5-point Likert scale (1=strongly disagree to 5=strongly agree). Raw scores range from 6-30 with higher scores representing more endorsement of meaning and life. Raw scores are converted to T-scores based on population norms with a mean of 50 and standard deviation of 10. Therefore a score of 60 represents 1 standard deviation above the population average and indicates a high level of meaning and purpose. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive and Affective Mindfulness Scale-Revised (CAMS-R)Baseline, 8 weeksThe CAMS-R is a 12-item scale measuring mindfulness by using language that is not representative of any particular meditation training or practice. It uses a 4-point Likert scale with responses ranging from 1 (Rarely/Not at all) to 4 (Almost always). Total scores range from 12-48. Higher scores indicate higher levels of mindfulness. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Emotional Distress-Anxiety-Short Form 4aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anxiety-Short Form 4a is a 4-item scale that assesses fear (fearfulness, panic), anxious misery (worry, dread), hyperarousal (tension, nervousness, restlessness), and somatic symptoms related to arousal (racing heart, dizziness). It uses a 5-point Likert scale (1=never to 5=always). Raw scores range from 4-20 and are standardized to T-scores based on population averages (mean 50 and standard deviation 10). A score less than 55 is within normal limits. A score between 55-59.9 represents mild anxiety. A score greater than 60-69.9 represents moderate anxiety and a score of 70 or greater represents severe anxiety. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Emotional Distress-Anger-Short Form 5aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anger-Short Form 5a item is a 5-item scale that assesses angry mood (irritability, frustration), negative social cognitions (interpersonal sensitivity, envy, disagreeableness), and efforts to control anger. It uses a 5-point Likert scale (1=never to 5=always). Raw scores range from 5-25 and are standardized to T-scores based on population averages (mean 50 and standard deviation 10). A score less than 55 is within normal limits. A score between 55-59.9 represents mild anger; 60-69.9 represents moderate anger and 70 or greater represents severe anger. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Global Physical HealthBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Global Physical Health is a 2-item scale that assesses overall evaluation of one's physical health. It is based on the well-validated Rand measure, assessing general self-rated physical health, physical function, pain, and fatigue. It uses a 5-point Likert scale (1=poor to 5=excellent). Raw scores range from 2-10 and are standardized to T-scores with a population average of 50 and standard deviation of 10. Suggested cut points include 58 or higher = excellent; 50-57.9 = very good; 42-49.9 = good; 35-41.9 = fair, and less than 35 = poor. Change scores are reported from mixed effects models that utilize the entire population.
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short FormBaseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form is an 18-item measure consisting of 5 positive coping strategies (acceptance, positive refocusing, planning, positive reappraisal, putting into perspective) and 4 negative strategies (rumination, catastrophizing, self-blame, other-blame). Total scores range from 18-90 with higher scores representing more cognitive emotional regulation. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Acceptance)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form acceptance subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater acceptance coping. Change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Refocusing)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form positive refocusing subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater positive refocusing coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Planning)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form planning subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater planning. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Reappraisal)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form positive reappraisal subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater positive reappraisal. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Putting Into Perspective)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form putting into perspective subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater putting into perspective coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline in the Zarit Burden Interview Short Form (ZBI-12) ScoreBaseline, 8 weeksThe ZBI-12 is a 12-item (SF) version of the original 29-item questionnaire measures role strain and personal strain. Items are measured on a 5-point Likert scale (0=never to 4=nearly always). Scores range from 0-48 with lower scores representing less burden. Within group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Catastrophizing)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form catastrophizing subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater catastrophizing coping. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Self-Blame)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form self-blame subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater self-blame as a coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Other-Blame)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form other-blame subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater blaming others as a coping strategy. Change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Emotional Support-Short Form 4aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Support-Short Form 4a is a 4-item scale that assesses perceived feelings of being cared for and valued as a person and having confidant relationships. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Emotional Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of emotional support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Informational Support-Short Form 4aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Informational Support-Short Form 4a is a 4-item scale that assesses perceived availability of helpful information or advice. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Informational Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of informational support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Instrumental Support-Short Form 4aBaseline, 8 weeksThe PROMIS Instrumental Support-Short Form 4a is a 4-item scale that assesses perceived availability of assistance with material, cognitive or task performance. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Instrumental Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of instrumental support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS General Self-Efficacy-Short Form 4aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) General Self-Efficacy-Short Form 4a is a 4-item scale that assesses confidence in ability to successfully perform specific tasks or behaviors related to one's health in a variety of situations. Items are measured on a 5-point Likert scale (1=I am not at all confident to 5=I am very confident). Raw scores range from 4-20. The PROMIS General Self-Efficacy item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of self-efficacy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline in Mean NPI-Q Distress ScoresBaseline, 8 weeksThe Neuropsychiatric Inventory (NPI-Q) Caregiver Distress subscale uses a 6-point scale with 12 items and scores ranging from 0-60. The NPI-Q measures the degree of distress associated with symptoms associated with dementia e.g., delusions, appetite change, and anxiety. Higher scores indicate more distress. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on PROMIS Self-Efficacy for Managing Emotions-Short Form 4aBaseline, 8 weeksThe Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Emotions-Short Form 4a is a 4-item scale that assesses confidence to manage/control symptoms of anxiety, depression, helplessness, discouragement, frustration, disappointment and anger. Items are measured using a 5-point Likert scale (1=I am not at all confident to 5=I am very confident). Raw scores range from 4-20. The PROMIS Self-Efficacy for Managing Emotions item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of managing emotion. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline in the Family Conflict Strategies for Care SubscaleBaseline, 8 weeksThe FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The first subscale measures conflict around definitions of the illness and strategies for care (4 items). Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline in the Family Conflict Scale Attitudes and Actions Toward the Patient SubscaleBaseline, 8 weeksThe FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The second subscale measures conflict around family members' attitudes and action toward the patient (4 items) Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline on Family Conflict Scale (FCS) Actions and Attitudes Toward the Caregiver SubscaleBaseline, 8 weeksThe FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The third subscale measures conflict around family members' actions and attitudes around the caregiver (4 items). Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. This measure was requested from the primary caregiver only. Change scores are reported from mixed effects models controlling for the severity of dementia in the care recipient and dependencies in the data (individuals within cohorts).
Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Rumination)Baseline, 8 weeksCognitive Emotional Regulation Questionnaire (CERQ)-Short Form rumination subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater rumination. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).
Change From Baseline in the Family Satisfaction Scale (FSS) Scoreup to 8 weeksThe FSS is a 10-item scale which uses a 5-point Likert scale (1=very dissatisfied to 5=extremely satisfied). Total scores range from 10-50 with higher scores representing more endorsement of family satisfaction. The FSS was administered at Baseline and Week 8. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Countries

United States

Participant flow

Pre-assignment details

Primary Caregivers and Care Partners were enrolled as dyads. A total of 28 dyads and 1 additional Primary Caregiver were included in the analysis. One Care Partner was not enrolled as planned after the Primary Caregiver had already been enrolled.

Participants by arm

ArmCount
Telephone-delivered Mindfulness
Participating Primary Caregivers and Care Partners receive mindfulness training in 8 weekly telephone sessions plus one retreat between weeks 5 and 6.
57
Total57

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyInadequate deafness interpreter service1
Overall StudyWithdrawal by Subject4

Baseline characteristics

CharacteristicTelephone-delivered Mindfulness
Age, Continuous
Care Partners
53 years
STANDARD_DEVIATION 20
Age, Continuous
Primary Caregivers
61 years
STANDARD_DEVIATION 9
Annual Household Income
Care Partners
$21-40K per year
10 Participants
Annual Household Income
Care Partners
$41-60K per year
4 Participants
Annual Household Income
Care Partners
$61-80K per year
3 Participants
Annual Household Income
Care Partners
Less than $20K per year
4 Participants
Annual Household Income
Care Partners
More than $80K per year
4 Participants
Annual Household Income
Care Partners
Preferred Not to Answer
3 Participants
Annual Household Income
Primary Caregivers
$21-40K per year
5 Participants
Annual Household Income
Primary Caregivers
$41-60K per year
6 Participants
Annual Household Income
Primary Caregivers
$61-80K per year
3 Participants
Annual Household Income
Primary Caregivers
Less than $20K per year
9 Participants
Annual Household Income
Primary Caregivers
More than $80K per year
3 Participants
Annual Household Income
Primary Caregivers
Preferred Not to Answer
3 Participants
Ethnicity (NIH/OMB)
Care Partners
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Care Partners
Not Hispanic or Latino
28 Participants
Ethnicity (NIH/OMB)
Care Partners
Unknown or Not Reported
0 Participants
Ethnicity (NIH/OMB)
Primary Caregivers
Hispanic or Latino
1 Participants
Ethnicity (NIH/OMB)
Primary Caregivers
Not Hispanic or Latino
28 Participants
Ethnicity (NIH/OMB)
Primary Caregivers
Unknown or Not Reported
0 Participants
Highest Education Level Completed
Care Partners
Advanced Degree
4 Participants
Highest Education Level Completed
Care Partners
Bachelor's Degree
9 Participants
Highest Education Level Completed
Care Partners
High School or less
7 Participants
Highest Education Level Completed
Care Partners
Some College
8 Participants
Highest Education Level Completed
Primary Caregivers
Advanced Degree
5 Participants
Highest Education Level Completed
Primary Caregivers
Bachelor's Degree
10 Participants
Highest Education Level Completed
Primary Caregivers
High School or less
2 Participants
Highest Education Level Completed
Primary Caregivers
Some College
12 Participants
Number of Participants Working Outside the Home
Care Partners
16 Participants
Number of Participants Working Outside the Home
Primary Caregivers
15 Participants
Race (NIH/OMB)
Care Partners
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Care Partners
Asian
0 Participants
Race (NIH/OMB)
Care Partners
Black or African American
28 Participants
Race (NIH/OMB)
Care Partners
More than one race
0 Participants
Race (NIH/OMB)
Care Partners
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Care Partners
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Care Partners
White
0 Participants
Race (NIH/OMB)
Primary Caregivers
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Primary Caregivers
Asian
0 Participants
Race (NIH/OMB)
Primary Caregivers
Black or African American
29 Participants
Race (NIH/OMB)
Primary Caregivers
More than one race
0 Participants
Race (NIH/OMB)
Primary Caregivers
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Primary Caregivers
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Primary Caregivers
White
0 Participants
Region of Enrollment
United States
57 Participants
Sex: Female, Male
Care Partners
Female
19 Participants
Sex: Female, Male
Care Partners
Male
9 Participants
Sex: Female, Male
Primary Caregivers
Female
26 Participants
Sex: Female, Male
Primary Caregivers
Male
3 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 290 / 28
other
Total, other adverse events
2 / 294 / 28
serious
Total, serious adverse events
0 / 290 / 28

Outcome results

Primary

Number of Participants Attending at Least 6 Telephone Sessions

The instructor will conduct a role call to take attendance at the beginning of each of the 8 class sessions and 1 retreat session. Eighty-five percent of participants who start the intervention will complete at least 6 out of 9 intervention sessions. Attendance used as a proxy to assess intervention acceptability.

Time frame: 8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Primary CaregiversNumber of Participants Attending at Least 6 Telephone Sessions27 Participants
Care PartnersNumber of Participants Attending at Least 6 Telephone Sessions23 Participants
Total PopulationNumber of Participants Attending at Least 6 Telephone Sessions50 Participants
Primary

Percent of Dyads Who Endorse the Program

The intervention will be acceptable to informal caregiving teams as evidenced by an 85 percent (95% Confidence Interval (CI): 72.5, 97.5) endorsement of the program in post-participation interviews. Calculated based on responses to open-ended questions regarding participants' experiences of the intervention. Examples of questions are: how valuable or beneficial was the mindfulness training to you? and what challenges did you have with the training? and what did you expect from the training that you did not get?. Endorsement was considered positive if the expressions of value outweighed challenges (i.e., positive comments outweighed negative comments by dyad). Data reported as caregiving teams (dyads) in accordance with the protocol.

Time frame: 8 weeks

Population: Of the 25 dyads completed, 1 Primary Caregiver and 1 Care Partner were unavailable to complete the interview thus eliminating 2 dyads and leaving 23 dyads for this evaluation.

ArmMeasureValue (NUMBER)
Primary CaregiversPercent of Dyads Who Endorse the Program100 percent of dyads
Secondary

Change From Baseline in Intolerance of Uncertainty Scale (IUS-12) Inhibitory Subscale Score

The inhibitory subscale of the Intolerance of Uncertainty Scale (IUS-12) is a 5-item measure. The measure uses a 5-point Likert scale (1=not at all like me to 5=entirely like me). Total scores range from 5-25, with lower scores reflecting more tolerance of uncertain situations. IUS-12 was administered at baseline and at 8 weeks. Within group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: up to 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Inhibitory Subscale Score-0.81 score on a scale
Care PartnersChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Inhibitory Subscale Score-1.17 score on a scale
Total PopulationChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Inhibitory Subscale Score-0.97 score on a scale
Secondary

Change From Baseline in Intolerance of Uncertainty Scale (IUS-12) Prospective Subscale Score

The prospective anxiety subscale of the Intolerance of Uncertainty Scale (IUS-12) is a 7-item measure. The measure uses a 5-point Likert scale (1=not at all like me to 5=entirely like me). Scores range from 7-35, with lower scores reflecting more tolerance of uncertain situations. IUS-12 was administered at Baseline and at 8 weeks. Change scores are reported from paired t-tests for within-group assessments and from mixed effects models for the total population controlling for caregiving role, severity of dementia in the care recipient and dependencies in the data (individuals within families within cohorts).

Time frame: up to 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Prospective Subscale Score-1.11 score on a scale
Care PartnersChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Prospective Subscale Score-1.00 score on a scale
Total PopulationChange From Baseline in Intolerance of Uncertainty Scale (IUS-12) Prospective Subscale Score-1.16 score on a scale
Secondary

Change From Baseline in Mean NPI-Q Distress Scores

The Neuropsychiatric Inventory (NPI-Q) Caregiver Distress subscale uses a 6-point scale with 12 items and scores ranging from 0-60. The NPI-Q measures the degree of distress associated with symptoms associated with dementia e.g., delusions, appetite change, and anxiety. Higher scores indicate more distress. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: Three Care Partners who provided no direct care did not complete this measure. One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments. One Primary Caregiver did not complete the measure at Baseline.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in Mean NPI-Q Distress Scores-2.31 units on a scale
Care PartnersChange From Baseline in Mean NPI-Q Distress Scores-1.24 units on a scale
Total PopulationChange From Baseline in Mean NPI-Q Distress Scores-1.8 units on a scale
Secondary

Change From Baseline in the Family Conflict Scale Attitudes and Actions Toward the Patient Subscale

The FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The second subscale measures conflict around family members' attitudes and action toward the patient (4 items) Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessments and another Care Partner completed only part of the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in the Family Conflict Scale Attitudes and Actions Toward the Patient Subscale-0.30 score on a scale
Care PartnersChange From Baseline in the Family Conflict Scale Attitudes and Actions Toward the Patient Subscale-0.43 score on a scale
Total PopulationChange From Baseline in the Family Conflict Scale Attitudes and Actions Toward the Patient Subscale-0.34 score on a scale
Secondary

Change From Baseline in the Family Conflict Strategies for Care Subscale

The FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The first subscale measures conflict around definitions of the illness and strategies for care (4 items). Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention did not complete the post-intervention assessments and another Care Partner completed only part of the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in the Family Conflict Strategies for Care Subscale-0.30 score on a scale
Care PartnersChange From Baseline in the Family Conflict Strategies for Care Subscale-0.17 score on a scale
Total PopulationChange From Baseline in the Family Conflict Strategies for Care Subscale-0.23 score on a scale
Secondary

Change From Baseline in the Family Satisfaction Scale (FSS) Score

The FSS is a 10-item scale which uses a 5-point Likert scale (1=very dissatisfied to 5=extremely satisfied). Total scores range from 10-50 with higher scores representing more endorsement of family satisfaction. The FSS was administered at Baseline and Week 8. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: up to 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments and another Care Partner did not complete all of the measures.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in the Family Satisfaction Scale (FSS) Score2.78 score on a scale
Care PartnersChange From Baseline in the Family Satisfaction Scale (FSS) Score4.30 score on a scale
Total PopulationChange From Baseline in the Family Satisfaction Scale (FSS) Score3.12 score on a scale
Secondary

Change From Baseline in the Zarit Burden Interview Short Form (ZBI-12) Score

The ZBI-12 is a 12-item (SF) version of the original 29-item questionnaire measures role strain and personal strain. Items are measured on a 5-point Likert scale (0=never to 4=nearly always). Scores range from 0-48 with lower scores representing less burden. Within group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: Two Care Partners are missing Baseline data due to an electronic glitch. One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline in the Zarit Burden Interview Short Form (ZBI-12) Score-2.5 score on a scale
Care PartnersChange From Baseline in the Zarit Burden Interview Short Form (ZBI-12) Score-3.6 score on a scale
Total PopulationChange From Baseline in the Zarit Burden Interview Short Form (ZBI-12) Score-2.9 score on a scale
Secondary

Change From Baseline on Cognitive and Affective Mindfulness Scale-Revised (CAMS-R)

The CAMS-R is a 12-item scale measuring mindfulness by using language that is not representative of any particular meditation training or practice. It uses a 4-point Likert scale with responses ranging from 1 (Rarely/Not at all) to 4 (Almost always). Total scores range from 12-48. Higher scores indicate higher levels of mindfulness. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: The CAMS-R was added late and is unavailable at Baseline for the first 7 participants in the study (1st 4 Primary Caregivers, 1st 3 Care Partners). One Primary Caregiver did not complete the measure at Baseline or 8 weeks. One Care Partner who completed the intervention did not complete the measure at 8 weeks.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive and Affective Mindfulness Scale-Revised (CAMS-R)2.77 units on a scale
Care PartnersChange From Baseline on Cognitive and Affective Mindfulness Scale-Revised (CAMS-R)2.04 units on a scale
Total PopulationChange From Baseline on Cognitive and Affective Mindfulness Scale-Revised (CAMS-R)2.5 units on a scale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form is an 18-item measure consisting of 5 positive coping strategies (acceptance, positive refocusing, planning, positive reappraisal, putting into perspective) and 4 negative strategies (rumination, catastrophizing, self-blame, other-blame). Total scores range from 18-90 with higher scores representing more cognitive emotional regulation. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form1.48 score on a scale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form0.88 score on a scale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form1.29 score on a scale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Acceptance)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form acceptance subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater acceptance coping. Change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Acceptance)0.07 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Acceptance)-0.46 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Acceptance)-0.22 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Catastrophizing)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form catastrophizing subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater catastrophizing coping. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Catastrophizing)-0.37 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Catastrophizing)-0.13 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Catastrophizing)-0.30 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Other-Blame)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form other-blame subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater blaming others as a coping strategy. Change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Other-Blame)0.11 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Other-Blame)0.21 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Other-Blame)0.14 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Planning)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form planning subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater planning. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment. Another Care Partner declined to answer this question at Baseline.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Planning)0.15 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Planning)-0.57 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Planning)-0.21 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Reappraisal)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form positive reappraisal subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater positive reappraisal. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Reappraisal)0.07 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Reappraisal)0.25 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Reappraisal)0.25 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Refocusing)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form positive refocusing subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater positive refocusing coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Refocusing)0.15 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Refocusing)1.08 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Positive Refocusing)0.55 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Putting Into Perspective)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form putting into perspective subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater putting into perspective coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Putting Into Perspective)-0.41 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Putting Into Perspective)0.67 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Putting Into Perspective)0.23 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Rumination)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form rumination subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater rumination. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Rumination)-1.0 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Rumination)-0.04 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Rumination)-0.49 score on a subscale
Secondary

Change From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Self-Blame)

Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form self-blame subscale consisting of two questions. The subscale scores range from 2-10 with higher scores representing greater self-blame as a coping strategy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving roles, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Self-Blame)-0.52 score on a subscale
Care PartnersChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Self-Blame)0.08 score on a subscale
Total PopulationChange From Baseline on Cognitive Emotional Regulation Questionnaire (CERQ)-Short Form (Self-Blame)-0.30 score on a subscale
Secondary

Change From Baseline on Family Conflict Scale (FCS) Actions and Attitudes Toward the Caregiver Subscale

The FCS is a 12-item scale that measures the degree of conflict the family experiences about the seriousness of the care recipient's condition, concerns about the care recipient's safety, what the care recipient can do for him/herself, and whether a nursing home is indicated. The third subscale measures conflict around family members' actions and attitudes around the caregiver (4 items). Items are measured on a 4-point Likert scale (1=no disagreement to 4=quite a bit of disagreement). The total scores range from 4-16 with lower scores representing less family conflict. This measure was requested from the primary caregiver only. Change scores are reported from mixed effects models controlling for the severity of dementia in the care recipient and dependencies in the data (individuals within cohorts).

Time frame: Baseline, 8 weeks

Population: This subscale was administered only to the Primary Caregivers. Data was unavailable at follow-up for two Primary Caregivers who completed the intervention.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on Family Conflict Scale (FCS) Actions and Attitudes Toward the Caregiver Subscale-0.06 score on a scale
Secondary

Change From Baseline on PROMIS Emotional Distress-Anger-Short Form 5a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anger-Short Form 5a item is a 5-item scale that assesses angry mood (irritability, frustration), negative social cognitions (interpersonal sensitivity, envy, disagreeableness), and efforts to control anger. It uses a 5-point Likert scale (1=never to 5=always). Raw scores range from 5-25 and are standardized to T-scores based on population averages (mean 50 and standard deviation 10). A score less than 55 is within normal limits. A score between 55-59.9 represents mild anger; 60-69.9 represents moderate anger and 70 or greater represents severe anger. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the study was unavailable to complete the post-intervention questionnaire.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Emotional Distress-Anger-Short Form 5a-0.79 T score
Care PartnersChange From Baseline on PROMIS Emotional Distress-Anger-Short Form 5a2.21 T score
Total PopulationChange From Baseline on PROMIS Emotional Distress-Anger-Short Form 5a0.67 T score
Secondary

Change From Baseline on PROMIS Emotional Distress-Anxiety-Short Form 4a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anxiety-Short Form 4a is a 4-item scale that assesses fear (fearfulness, panic), anxious misery (worry, dread), hyperarousal (tension, nervousness, restlessness), and somatic symptoms related to arousal (racing heart, dizziness). It uses a 5-point Likert scale (1=never to 5=always). Raw scores range from 4-20 and are standardized to T-scores based on population averages (mean 50 and standard deviation 10). A score less than 55 is within normal limits. A score between 55-59.9 represents mild anxiety. A score greater than 60-69.9 represents moderate anxiety and a score of 70 or greater represents severe anxiety. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Emotional Distress-Anxiety-Short Form 4a-0.9 T-score
Care PartnersChange From Baseline on PROMIS Emotional Distress-Anxiety-Short Form 4a0.06 T-score
Total PopulationChange From Baseline on PROMIS Emotional Distress-Anxiety-Short Form 4a0.67 T-score
Secondary

Change From Baseline on PROMIS Emotional Support-Short Form 4a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Support-Short Form 4a is a 4-item scale that assesses perceived feelings of being cared for and valued as a person and having confidant relationships. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Emotional Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of emotional support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessments and a Primary Caregiver completed only part of the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Emotional Support-Short Form 4a0.48 T score
Care PartnersChange From Baseline on PROMIS Emotional Support-Short Form 4a1.39 T score
Total PopulationChange From Baseline on PROMIS Emotional Support-Short Form 4a0.89 T score
Secondary

Change From Baseline on PROMIS General Self-Efficacy-Short Form 4a

The Patient-Reported Outcomes Measurement Information System (PROMIS) General Self-Efficacy-Short Form 4a is a 4-item scale that assesses confidence in ability to successfully perform specific tasks or behaviors related to one's health in a variety of situations. Items are measured on a 5-point Likert scale (1=I am not at all confident to 5=I am very confident). Raw scores range from 4-20. The PROMIS General Self-Efficacy item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of self-efficacy. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable to complete the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS General Self-Efficacy-Short Form 4a2.51 T scores
Care PartnersChange From Baseline on PROMIS General Self-Efficacy-Short Form 4a1.79 T scores
Total PopulationChange From Baseline on PROMIS General Self-Efficacy-Short Form 4a2.2 T scores
Secondary

Change From Baseline on PROMIS Global Physical Health

The Patient-Reported Outcomes Measurement Information System (PROMIS) Global Physical Health is a 2-item scale that assesses overall evaluation of one's physical health. It is based on the well-validated Rand measure, assessing general self-rated physical health, physical function, pain, and fatigue. It uses a 5-point Likert scale (1=poor to 5=excellent). Raw scores range from 2-10 and are standardized to T-scores with a population average of 50 and standard deviation of 10. Suggested cut points include 58 or higher = excellent; 50-57.9 = very good; 42-49.9 = good; 35-41.9 = fair, and less than 35 = poor. Change scores are reported from mixed effects models that utilize the entire population.

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessment.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Global Physical Health-1.85 T score
Care PartnersChange From Baseline on PROMIS Global Physical Health-1.16 T score
Total PopulationChange From Baseline on PROMIS Global Physical Health-1.45 T score
Secondary

Change From Baseline on PROMIS Informational Support-Short Form 4a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Informational Support-Short Form 4a is a 4-item scale that assesses perceived availability of helpful information or advice. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Informational Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of informational support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessments and a Primary Caregiver completed only part of the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Informational Support-Short Form 4a2.72 T score
Care PartnersChange From Baseline on PROMIS Informational Support-Short Form 4a2.05 T score
Total PopulationChange From Baseline on PROMIS Informational Support-Short Form 4a2.65 T score
Secondary

Change From Baseline on PROMIS Instrumental Support-Short Form 4a

The PROMIS Instrumental Support-Short Form 4a is a 4-item scale that assesses perceived availability of assistance with material, cognitive or task performance. Item responses use a 5-point LIkert scale (1=never to 5=always). Raw scores range from 4-20. The PROMIS Instrumental Support item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of instrumental support. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for the post-intervention assessments and a Primary Caregiver completed only part of the post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Instrumental Support-Short Form 4a0.87 T score
Care PartnersChange From Baseline on PROMIS Instrumental Support-Short Form 4a0.35 T score
Total PopulationChange From Baseline on PROMIS Instrumental Support-Short Form 4a0.65 T score
Secondary

Change From Baseline on PROMIS Meaning and Purpose-Short Form 6a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Meaning and Purpose-Short Form 6a is a 6-item scale that assesses a sense that life has purpose and there are good reasons for living, including hopefulness, optimism, goal-directedness, and feelings that one's life is worthy. It uses a 5-point Likert scale (1=strongly disagree to 5=strongly agree). Raw scores range from 6-30 with higher scores representing more endorsement of meaning and life. Raw scores are converted to T-scores based on population norms with a mean of 50 and standard deviation of 10. Therefore a score of 60 represents 1 standard deviation above the population average and indicates a high level of meaning and purpose. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: Data unavailable for one Care Partner who was unavailable at Week 8 and a Primary Caregiver who did not provide data at either Baseline or Week 8.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Meaning and Purpose-Short Form 6a3.18 T-score
Care PartnersChange From Baseline on PROMIS Meaning and Purpose-Short Form 6a2.23 T-score
Total PopulationChange From Baseline on PROMIS Meaning and Purpose-Short Form 6a2.7 T-score
Secondary

Change From Baseline on PROMIS Self-Efficacy for Managing Emotions-Short Form 4a

The Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Emotions-Short Form 4a is a 4-item scale that assesses confidence to manage/control symptoms of anxiety, depression, helplessness, discouragement, frustration, disappointment and anger. Items are measured using a 5-point Likert scale (1=I am not at all confident to 5=I am very confident). Raw scores range from 4-20. The PROMIS Self-Efficacy for Managing Emotions item is reported as a T score standardized to a population mean of 50 and standard deviation of 10 with higher scores reflecting more positive endorsement of managing emotion. Within-group change scores are reported based on paired t-tests. Total change scores are reported from mixed effects models controlling for caregiving role, the severity of dementia in the care recipient, and dependencies in the data (individuals within families within cohorts).

Time frame: Baseline, 8 weeks

Population: One Care Partner who completed the intervention was unavailable for post-intervention assessments.

ArmMeasureValue (MEAN)
Primary CaregiversChange From Baseline on PROMIS Self-Efficacy for Managing Emotions-Short Form 4a1.96 T score
Care PartnersChange From Baseline on PROMIS Self-Efficacy for Managing Emotions-Short Form 4a-0.06 T score
Total PopulationChange From Baseline on PROMIS Self-Efficacy for Managing Emotions-Short Form 4a0.98 T score

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026