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The HEART Study (Healthy Eating and Recovery Together)

A Mobile-Support Program to Facilitate Nutritional Caregiving in Head and Neck Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04552587
Enrollment
51
Registered
2020-09-17
Start date
2020-12-04
Completion date
2021-10-10
Last updated
2023-01-20

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

Conditions

Head and Neck Cancer, Nutrition Aspect of Cancer, Survivorship

Keywords

mHealth, Head and Neck Cancer, Survivorship, Caregiver

Brief summary

Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be enrolled to pilot test a nutrition support system with a care planning clinic visit and a caregiver mobile App. Participants will be asked to complete baseline and 6-week follow-up surveys. The clinic session (offered in person or remotely) will include a needs assessment and a tailored care plan with information, educational materials and referrals about participants' symptoms, behaviors, social concerns and caregiving tasks. After the visit, the program will provide an App for caregivers with follow-up resources and mobile support for one month.

Detailed description

The long-term goal of this research is to improve physical, emotional and social post-treatment outcomes in head and neck cancer survivors and caregivers by implementing a nutrition-focused mobile-Support program to prepare and support caregivers after treatment. Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be recruited to a single-arm intervention study to evaluate the feasibility, acceptability and short-term effects of a nutrition-focused mobile support system. The intervention includes 1) a clinic visit (offered in-person or virtually) with a tablet-based needs assessment at the end of or after completing treatment which will generate 2) a tailored care plan with messages, educational materials and referrals mapped to survivor and caregiver-endorsed concerns and 3) a caregiver App with encouragement, reminders and tips delivered through messaging and peer videos. Participants will complete baseline and 6-week follow-up surveys.

Interventions

BEHAVIORALHeart APP

The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

Patient Inclusion Criteria: * 18 years and older * Patients with stage I-IVB HNC of the upper aerodigestive tract (including lip/oral cavity, nasopharynx, salivary gland, oropharynx, hypopharynx, paranasal sinus, and larynx cancers and cutaneous cancers of the head and neck region) * In the last two weeks of treatment to 3 months following completion of primary treatment (i.e., any combination of surgery, chemotherapy and radiation therapy) within the past 3 months * Experienced nutritional challenges at the end of treatment as assessed in a 6-item screener Patient

Exclusion criteria

* head and neck cancer patients who do not undergo treatment * Patients who do not read or understand English * Patients who are cognitively impaired and cannot complete interviews, as judged by the referring health care provider * Patients who do not have a smartphone for use in the study Caregiver Inclusion Criteria: * 18 years and older * Provide care for a loved one with stage I-IVB head and neck cancer who has completed treatment Caregiver

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria6 week follow-up visitInvestigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate.
Intervention Delivery/ Fidelity6 week follow up visitNumber of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training).
Intervention ReachBaseline and 6 week follow up visitPercentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session.

Secondary

MeasureTime frameDescription
PROMIS Depression- Short Form (SF) v1.0 Form 8ABaseline and 6 week follow-up visitPROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of Never, Rarely, Sometimes, Often, and Always whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression.
Mean Score of Survivorship Readiness/Caregiver PreparednessBaseline and 6 week follow-up visitThe 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement.
Mean Score of Self-EfficacyBaseline and 6 week follow-up visitBased on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time? and How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors? Participants rated items on a 5-point Likert scale where 0=Not at all confident to 4= Completely confident. Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy.
Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Baseline and 6 week follow-up visitPROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement.
Caregiver BurdenBaseline and 6 week follow up visit4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress.
Ease of Mobile App Use/User Engagement4 weeks during app useNumber of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks).
Mean Score of Dyadic Coping/ Dyadic EfficacyBaseline and 6 week follow-up visitDyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 (never) to 5 (always). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up? Item was answered on a scale of 0 (not at all confident) to 10 (extremely confident), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement.
Percentage of Participants Rating App Satisfaction/ Perceived Importance6 week follow up visitRatings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts.
Process Monitoring DataAfter session completionResources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes
Change From Baseline in Nutritional Status ScaleBaseline and 6 week follow up visitInvestigator-developed 1 item: During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))?
Change From Baseline in Symptom Distress/Symptom ManagementBaseline and 6 week follow up visitAdapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all
Change From Baseline in Emotional SupportBaseline and 6 week follow up visitPROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean.
Change From Baseline in Symptom SeverityBaseline and 6 week follow up visitMD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being not present and 10 being as bad as you can imagine. Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms.
Number of Participants With Care Plan Use Endpoints6 week follow up visitNumber of participants of use of care plan after session, including patient and caregiver report of Referred to Care Plan again, Used Care Plan, Used educational materials, and Shared Care Plan with others.
Ease of Use/System Usability6 week follow up visit only (no baseline comparison)System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability.
Mean Score of Unmet NeedsBaseline and 6 week follow up visit30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported.

Countries

United States

Participant flow

Recruitment details

Head and neck cancer patients and caregivers were recruited at the end of radiation therapy.

Participants by arm

ArmCount
HEART
Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support.
46
Total46

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyLost to Follow-up4

Baseline characteristics

CharacteristicHEART
Age, Continuous
Caregivers
59 years
Age, Continuous
Patients
63 years
Ethnicity (NIH/OMB)
Caregiver
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Caregiver
Not Hispanic or Latino
23 Participants
Ethnicity (NIH/OMB)
Caregiver
Unknown or Not Reported
0 Participants
Ethnicity (NIH/OMB)
Patient
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Patient
Not Hispanic or Latino
23 Participants
Ethnicity (NIH/OMB)
Patient
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Caregivers
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Caregivers
Asian
0 Participants
Race (NIH/OMB)
Caregivers
Black or African American
3 Participants
Race (NIH/OMB)
Caregivers
More than one race
0 Participants
Race (NIH/OMB)
Caregivers
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Caregivers
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Caregivers
White
20 Participants
Race (NIH/OMB)
Patients
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Patients
Asian
0 Participants
Race (NIH/OMB)
Patients
Black or African American
4 Participants
Race (NIH/OMB)
Patients
More than one race
0 Participants
Race (NIH/OMB)
Patients
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Patients
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Patients
White
19 Participants
Region of Enrollment
United States
46 participants
Sex: Female, Male
Caregivers
Female
18 Participants
Sex: Female, Male
Caregivers
Male
5 Participants
Sex: Female, Male
Patients
Female
7 Participants
Sex: Female, Male
Patients
Male
16 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 230 / 23
other
Total, other adverse events
0 / 230 / 23
serious
Total, serious adverse events
0 / 230 / 23

Outcome results

Primary

Intervention Delivery/ Fidelity

Number of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training).

Time frame: 6 week follow up visit

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
HEART PatientsIntervention Delivery/ Fidelity19 Participants
Primary

Intervention Reach

Percentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session.

Time frame: Baseline and 6 week follow up visit

Population: 50 enrolled, 4 lost to follow up

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
HEART PatientsIntervention Reach46 Participants
Primary

Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria

Investigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate.

Time frame: 6 week follow-up visit

ArmMeasureGroupValue (NUMBER)
HEART PatientsNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaCare plan information was helpful emotionally17 participants
HEART PatientsNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaAmount of information in the care plan provided was appropriate18 participants
HEART PatientsNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaCare plan was helpful practically18 participants
HEART PatientsNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaSession timing was appropriate13 participants
HEART PatientsNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaSession made me feel prepared18 participants
HEART CaregiversNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaSession timing was appropriate9 participants
HEART CaregiversNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaSession made me feel prepared18 participants
HEART CaregiversNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaCare plan information was helpful emotionally15 participants
HEART CaregiversNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaCare plan was helpful practically18 participants
HEART CaregiversNumber of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability CriteriaAmount of information in the care plan provided was appropriate20 participants
Secondary

Caregiver Burden

4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress.

Time frame: Baseline and 6 week follow up visit

Population: Change in mean score from baseline to six weeks measured in caregivers only

ArmMeasureGroupValue (MEAN)
HEART PatientsCaregiver BurdenBaseline1.8 units on a scale
HEART PatientsCaregiver Burden6 Week follow up visit1.9 units on a scale
HEART PatientsCaregiver BurdenChange from baseline to 6 week follow up visit0.1 units on a scale
Comparison: We compared change from baseline to follow up in our single group of caregivers.p-value: 0.23Wilcoxon (Mann-Whitney)
Secondary

Change From Baseline in Emotional Support

PROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean.

Time frame: Baseline and 6 week follow up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsChange From Baseline in Emotional SupportBaseline56.0 T-Score
HEART PatientsChange From Baseline in Emotional Support6 week follow up visit55.7 T-Score
HEART PatientsChange From Baseline in Emotional SupportChange from baseline to 6 week follow up visit-0.3 T-Score
HEART CaregiversChange From Baseline in Emotional SupportBaseline52.0 T-Score
HEART CaregiversChange From Baseline in Emotional Support6 week follow up visit52.8 T-Score
HEART CaregiversChange From Baseline in Emotional SupportChange from baseline to 6 week follow up visit0.8 T-Score
Secondary

Change From Baseline in Nutritional Status Scale

Investigator-developed 1 item: During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))?

Time frame: Baseline and 6 week follow up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsChange From Baseline in Nutritional Status ScaleChange from baseline to 6 week follow up visit-0.5 score on a scale
HEART PatientsChange From Baseline in Nutritional Status ScaleBaseline3.5 score on a scale
HEART PatientsChange From Baseline in Nutritional Status Scale6 week follow up visit3.0 score on a scale
HEART CaregiversChange From Baseline in Nutritional Status Scale6 week follow up visit2.5 score on a scale
HEART CaregiversChange From Baseline in Nutritional Status ScaleBaseline3.3 score on a scale
HEART CaregiversChange From Baseline in Nutritional Status ScaleChange from baseline to 6 week follow up visit-0.8 score on a scale
Secondary

Change From Baseline in Symptom Distress/Symptom Management

Adapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all

Time frame: Baseline and 6 week follow up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: 6 week follow up4.2 score on a scale
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: Baseline2.5 score on a scale
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: Baseline to 6 week follow up visit0.2 score on a scale
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: 6 week follow up2.7 score on a scale
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: Baseline to 6 week follow up visit-0.4 score on a scale
HEART PatientsChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: Baseline4.6 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: Baseline to 6 week follow up visit-1.2 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: Baseline5.6 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: 6 week follow up4.3 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Distress: Baseline to 6 week follow up visit-1.3 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: Baseline3.7 score on a scale
HEART CaregiversChange From Baseline in Symptom Distress/Symptom ManagementSymptom Management: 6 week follow up2.6 score on a scale
Secondary

Change From Baseline in Symptom Severity

MD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being not present and 10 being as bad as you can imagine. Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms.

Time frame: Baseline and 6 week follow up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsChange From Baseline in Symptom Severity6 week follow up visit2.0 score on a scale
HEART PatientsChange From Baseline in Symptom SeverityChange from baseline to 6 week follow up visit-1.0 score on a scale
HEART PatientsChange From Baseline in Symptom SeverityBaseline3.0 score on a scale
Secondary

Ease of Mobile App Use/User Engagement

Number of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks).

Time frame: 4 weeks during app use

Population: Measured in Caregivers only. (23 caregivers given 2 prompts per week for 4 weeks= 184 prompts).

ArmMeasureValue (NUMBER)
HEART PatientsEase of Mobile App Use/User Engagement70 number of missed prompts
Secondary

Ease of Use/System Usability

System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability.

Time frame: 6 week follow up visit only (no baseline comparison)

Population: System Usability Scale only measured in Caregivers.

ArmMeasureValue (MEAN)
HEART PatientsEase of Use/System Usability76 score on a scale
Secondary

Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)

PROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement.

Time frame: Baseline and 6 week follow-up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Baseline47.7 T-Score
HEART PatientsHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Change from baseline to 6 week follow up visit-1.0 T-Score
HEART PatientsHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)6 week follow up visit46.6 T-Score
HEART CaregiversHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Baseline49.0 T-Score
HEART CaregiversHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Change from baseline to 6 week follow up visit-0.5 T-Score
HEART CaregiversHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)6 week follow up visit48.5 T-Score
Patient HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)6 week follow up visit44.6 T-Score
Patient HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Baseline42.4 T-Score
Patient HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Change from baseline to 6 week follow up visit2.2 T-Score
Caregiver HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Baseline50.4 T-Score
Caregiver HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)Change from baseline to 6 week follow up visit-0.05 T-Score
Caregiver HRQOL Physical ScoresHealth-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)6 week follow up visit50.4 T-Score
Secondary

Mean Score of Dyadic Coping/ Dyadic Efficacy

Dyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 (never) to 5 (always). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up? Item was answered on a scale of 0 (not at all confident) to 10 (extremely confident), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement.

Time frame: Baseline and 6 week follow-up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: Baseline4.3 score on a scale
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: 6 week follow up visit4.2 score on a scale
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: Change from baseline to 6 week follow up-0.2 score on a scale
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: Baseline9.0 score on a scale
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: 6 week follow up visit8.3 score on a scale
HEART PatientsMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: Change from baseline to 6 week follow up-0.6 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: 6 week follow up visit8.6 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: Baseline4.1 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: Baseline8.2 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: 6 week follow up visit4.1 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Efficacy: Change from baseline to 6 week follow up0.4 score on a scale
HEART CaregiversMean Score of Dyadic Coping/ Dyadic EfficacyDyadic Coping: Change from baseline to 6 week follow up0.0 score on a scale
Secondary

Mean Score of Self-Efficacy

Based on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time? and How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors? Participants rated items on a 5-point Likert scale where 0=Not at all confident to 4= Completely confident. Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy.

Time frame: Baseline and 6 week follow-up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsMean Score of Self-Efficacy6 week f/u Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care3.2 score on a scale
HEART PatientsMean Score of Self-EfficacyBaseline- Self Efficacy: adhering to recommended follow up care3.6 score on a scale
HEART PatientsMean Score of Self-EfficacyBaseline- Self Efficacy: confidence in obtaining cancer related advice3.3 score on a scale
HEART PatientsMean Score of Self-Efficacy6 week f/u visit- Self Efficacy: adhering to recommended follow up care3.6 score on a scale
HEART PatientsMean Score of Self-EfficacyChange- Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care-0.1 score on a scale
HEART PatientsMean Score of Self-EfficacyChange - Self Efficacy: adhering to recommended follow up care0.0 score on a scale
HEART CaregiversMean Score of Self-EfficacyChange - Self Efficacy: adhering to recommended follow up care0.1 score on a scale
HEART CaregiversMean Score of Self-EfficacyBaseline- Self Efficacy: confidence in obtaining cancer related advice3.0 score on a scale
HEART CaregiversMean Score of Self-Efficacy6 week f/u Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care2.8 score on a scale
HEART CaregiversMean Score of Self-EfficacyChange- Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care-0.2 score on a scale
HEART CaregiversMean Score of Self-EfficacyBaseline- Self Efficacy: adhering to recommended follow up care3.3 score on a scale
HEART CaregiversMean Score of Self-Efficacy6 week f/u visit- Self Efficacy: adhering to recommended follow up care3.4 score on a scale
Secondary

Mean Score of Survivorship Readiness/Caregiver Preparedness

The 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement.

Time frame: Baseline and 6 week follow-up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsMean Score of Survivorship Readiness/Caregiver PreparednessBaseline4.5 score on a scale
HEART PatientsMean Score of Survivorship Readiness/Caregiver Preparedness6 week follow up visit4.6 score on a scale
HEART PatientsMean Score of Survivorship Readiness/Caregiver PreparednessChange from baseline to 6 weeks follow up0.1 score on a scale
HEART CaregiversMean Score of Survivorship Readiness/Caregiver PreparednessBaseline4.6 score on a scale
HEART CaregiversMean Score of Survivorship Readiness/Caregiver Preparedness6 week follow up visit4.5 score on a scale
HEART CaregiversMean Score of Survivorship Readiness/Caregiver PreparednessChange from baseline to 6 weeks follow up-0.1 score on a scale
Secondary

Mean Score of Unmet Needs

30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported.

Time frame: Baseline and 6 week follow up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsMean Score of Unmet NeedsBaseline endorsed needs9.5 score on a scale
HEART PatientsMean Score of Unmet Needs6 week follow up visit endorsed needs8.9 score on a scale
HEART PatientsMean Score of Unmet NeedsChange from baseline to 6 week follow up visit-0.6 score on a scale
HEART CaregiversMean Score of Unmet NeedsBaseline endorsed needs8.6 score on a scale
HEART CaregiversMean Score of Unmet Needs6 week follow up visit endorsed needs7.5 score on a scale
HEART CaregiversMean Score of Unmet NeedsChange from baseline to 6 week follow up visit-1.0 score on a scale
Secondary

Number of Participants With Care Plan Use Endpoints

Number of participants of use of care plan after session, including patient and caregiver report of Referred to Care Plan again, Used Care Plan, Used educational materials, and Shared Care Plan with others.

Time frame: 6 week follow up visit

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
HEART PatientsNumber of Participants With Care Plan Use EndpointsUsed Care Plan10 Participants
HEART PatientsNumber of Participants With Care Plan Use EndpointsReferred to Care plan again17 Participants
HEART PatientsNumber of Participants With Care Plan Use EndpointsUsed educational materials10 Participants
HEART PatientsNumber of Participants With Care Plan Use EndpointsShared Care Plan with others7 Participants
HEART CaregiversNumber of Participants With Care Plan Use EndpointsShared Care Plan with others4 Participants
HEART CaregiversNumber of Participants With Care Plan Use EndpointsReferred to Care plan again20 Participants
HEART CaregiversNumber of Participants With Care Plan Use EndpointsUsed Care Plan8 Participants
HEART CaregiversNumber of Participants With Care Plan Use EndpointsUsed educational materials16 Participants
Secondary

Percentage of Participants Rating App Satisfaction/ Perceived Importance

Ratings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts.

Time frame: 6 week follow up visit

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
HEART PatientsPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp support received helped you provide care for your loved one17 Participants
HEART PatientsPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp provided practical tips10 Participants
HEART PatientsPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp support was helpful emotionally15 Participants
HEART PatientsPercentage of Participants Rating App Satisfaction/ Perceived ImportanceAmount of app information was appropriate15 Participants
HEART CaregiversPercentage of Participants Rating App Satisfaction/ Perceived ImportanceAmount of app information was appropriate16 Participants
HEART CaregiversPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp support received helped you provide care for your loved one13 Participants
HEART CaregiversPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp support was helpful emotionally11 Participants
HEART CaregiversPercentage of Participants Rating App Satisfaction/ Perceived ImportanceApp provided practical tips12 Participants
Secondary

Process Monitoring Data

Resources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes

Time frame: After session completion

ArmMeasureGroupValue (MEAN)
HEART PatientsProcess Monitoring DataLength of full session51 minutes
HEART PatientsProcess Monitoring DataLength of nursing visit (within full session)13 minutes
HEART PatientsProcess Monitoring DataLength of App Training12 minutes
Secondary

PROMIS Depression- Short Form (SF) v1.0 Form 8A

PROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of Never, Rarely, Sometimes, Often, and Always whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression.

Time frame: Baseline and 6 week follow-up visit

ArmMeasureGroupValue (MEAN)
HEART PatientsPROMIS Depression- Short Form (SF) v1.0 Form 8ABaseline51.2 T-Score
HEART PatientsPROMIS Depression- Short Form (SF) v1.0 Form 8A6 week follow up visit48.0 T-Score
HEART PatientsPROMIS Depression- Short Form (SF) v1.0 Form 8AChange from baseline to 6 week follow up visit-3.2 T-Score
HEART CaregiversPROMIS Depression- Short Form (SF) v1.0 Form 8ABaseline51.1 T-Score
HEART CaregiversPROMIS Depression- Short Form (SF) v1.0 Form 8A6 week follow up visit49.6 T-Score
HEART CaregiversPROMIS Depression- Short Form (SF) v1.0 Form 8AChange from baseline to 6 week follow up visit-1.5 T-Score

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