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Pair 2 Care: Peer Support for Caregivers of Black Americans Living With Dementia

Pair 2 Care: Peer Support for Caregivers of Black Americans Living With Dementia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06064955
Acronym
Pair 2 Care
Enrollment
15
Registered
2023-10-03
Start date
2023-10-05
Completion date
2024-07-11
Last updated
2025-02-13

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

Conditions

Dementia, Family Caregiver, Peer Support

Keywords

African American/Black

Brief summary

The purpose of this study is to test a peer support intervention for caregivers who are caring for a loved one living with dementia.

Detailed description

African Americans are twice as likely to develop Alzheimer's disease or a related form of dementia (ADRD) than their White counterparts. These individuals are, however, more often diagnosed later, creating additional physical, spiritual, psychosocial challenges for both the person living with ADRD and their family caregivers. African American ADRD caregivers are therefore at greater risk for adverse physiological and psychological health effects of caregiving, including significant burden and stress. Evidence suggests that peer to peer support using storytelling may be effective in assisting ADRD caregivers with surrogate healthcare decision making, an important aspect of palliative care. Access to and use of palliative care, a recognized approach to serious illness care symptom management, among African Americans are low. The impact of this healthcare inequity further reduces the quality of life for African American ADRD caregivers and subsequently their care recipients. Prior approaches to serious illness care have failed to address the needs of African Americans living with ADRD from a palliative care perspective. This inability to meet their needs leads to increased unmet caregiver needs. Peer mentorship, a relationship-centered person-to-person approach may reduce healthcare decision making burden within cultural groups such as African Americans through cultural tailoring by promoting oral traditions, personal contact, and storytelling. Our current study includes perspectives of lower socioeconomic status African American ADRD caregivers who have expressed the need for person-centered, non-judgmental, on-demand, culturally congruent caregiving support for advance care planning and healthcare decision making. Simultaneously, former caregivers retrospectively described perceived benefits of peer support while caregiving and their willingness to serve as peer mentors to current caregivers. Additional data from healthcare provider and community stakeholders support the need and potential benefits of peer support for ADRD caregivers. Based on these preliminary findings, there is an urgent need and exciting opportunity to address the unmet palliative care needs of current caregivers through peer support. For this innovative project, investigators will use the experiential expertise of former caregivers to help current caregivers with advance care planning and healthcare decision making. The purpose of this project is to use a stakeholder-informed approach in further developing and pilot testing the co-created Peer Support for Caregivers of African Americans Living with Alzheimer's Disease and Related Dementias (Pair2Care), a culturally sensitive caregiver peer support intervention. Aim: Conduct feasibility and acceptability testing of Pair 2 Care in current and trained former African American ADRD family caregiver peers paired based on congruent identity traits (e.g., relationship to care recipient, gender identity, etc.). Investigators will determine if Pair2Care is feasible and acceptable by evaluating satisfaction and appropriateness of the intervention for broader dissemination.

Interventions

BEHAVIORALPeer Support

Former caregivers will be paired with a current caregiver based on a similar personal attribute (e.g., relationship to care recipient). Each pair will complete at least five virtual face-to-face (video) interactions and at least 10 other interactions either via phone call, email, or text messaging over the 6-month time period.

Sponsors

Cambia Health Foundation
CollaboratorOTHER
Ohio State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

A model to explain factors impacting advance care planning among African Americans

Eligibility

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

Inclusion criteria

* African-American * English-speaking * Adult (18+) * Family caregivers of people living with dementia (current or former)

Exclusion criteria

* Non-African-American * Non-English-speaking * Under age 18 * Non-Family caregiver

Design outcomes

Primary

MeasureTime frameDescription
Medical Outcomes Study Social Support Survey (MOS SSS)Baseline and 6 months post baselineThis instrument contains 19 items that comprise 4 subscales: Emotional/Informational Support, Tangible Support, Affectionate Support, and Positive Social Interaction. Each item is scored on a 5 point Likert scale of 1 (none of the time) to 5 (all the time), with higher scores indicating more social support. Total and subscale scores are in a range of 1-5 calculated by taking the mean across items.

Countries

United States

Participant flow

Participants by arm

ArmCount
Peer Support
Former caregivers will be paired with a current caregivers Peer Support: Former caregivers will be paired with a current caregiver based on a similar personal attribute (e.g., relationship to care recipient). Each pair will complete at least five virtual face-to-face (video) interactions and at least 10 other interactions either via phone call, email, or text messaging over the 6-month time period.
15
Total15

Baseline characteristics

CharacteristicPeer Support
Age, Customized59.6 years
STANDARD_DEVIATION 13.5
Employment
Full-time
7 Participants
Employment
Homemaker
1 Participants
Employment
Not employed, retired
5 Participants
Employment
Part-time
2 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
14 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants
Marital Status
Married
8 Participants
Marital Status
Separated/Divorced
3 Participants
Marital Status
Single
3 Participants
Marital Status
Widowed
1 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
15 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
0 Participants
Region of Enrollment
United States
15 participants
Relationship to loved one with dementia
Daughter
10 Participants
Relationship to loved one with dementia
Friend/Neighbor
0 Participants
Relationship to loved one with dementia
Other
3 Participants
Relationship to loved one with dementia
Other relative
0 Participants
Relationship to loved one with dementia
Son
0 Participants
Relationship to loved one with dementia
Spouse
2 Participants
Sex: Female, Male
Female
15 Participants
Sex: Female, Male
Male
0 Participants
Years as caregiver to the loved one with dementia4.4 years
STANDARD_DEVIATION 3.4

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 15
other
Total, other adverse events
0 / 15
serious
Total, serious adverse events
0 / 15

Outcome results

Primary

Medical Outcomes Study Social Support Survey (MOS SSS)

This instrument contains 19 items that comprise 4 subscales: Emotional/Informational Support, Tangible Support, Affectionate Support, and Positive Social Interaction. Each item is scored on a 5 point Likert scale of 1 (none of the time) to 5 (all the time), with higher scores indicating more social support. Total and subscale scores are in a range of 1-5 calculated by taking the mean across items.

Time frame: Baseline and 6 months post baseline

Population: 1 participant was not able to complete the intervention due to the death of their spouse

ArmMeasureGroupValue (MEAN)Dispersion
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Emotional/Informational Support at Baseline3.75 score on a scaleStandard Deviation 1.03
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Emotional/Informational Support at 6 Months3.79 score on a scaleStandard Deviation 0.99
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Tangible support at Baseline3.68 score on a scaleStandard Deviation 1.02
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Tangible support at 6 months3.50 score on a scaleStandard Deviation 1.29
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Affectionate support at Baseline4.22 score on a scaleStandard Deviation 0.67
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Affectionate support at 6 months3.95 score on a scaleStandard Deviation 0.9
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Positive social interaction at Baseline4.11 score on a scaleStandard Deviation 0.72
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Positive social interaction at 6 months3.98 score on a scaleStandard Deviation 0.83
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Overall social support at Baseline3.88 score on a scaleStandard Deviation 0.75
Peer SupportMedical Outcomes Study Social Support Survey (MOS SSS)Overall social support at 6 months3.77 score on a scaleStandard Deviation 0.83

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