Trial Outcomes & Findings for Pair 2 Care: Peer Support for Caregivers of Black Americans Living With Dementia (NCT NCT06064955)

NCT ID: NCT06064955

Last Updated: 2025-02-13

Results Overview

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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

15 participants

Primary outcome timeframe

Baseline and 6 months post baseline

Results posted on

2025-02-13

Participant Flow

Participant milestones

Participant milestones
Measure
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.
Overall Study
STARTED
15
Overall Study
COMPLETED
14
Overall Study
NOT COMPLETED
1

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

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

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Peer Support
n=15 Participants
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.
Age, Customized
59.6 years
STANDARD_DEVIATION 13.5 • n=99 Participants
Sex: Female, Male
Female
15 Participants
n=99 Participants
Sex: Female, Male
Male
0 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
14 Participants
n=99 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants
n=99 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
Race (NIH/OMB)
Asian
0 Participants
n=99 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
Race (NIH/OMB)
Black or African American
15 Participants
n=99 Participants
Race (NIH/OMB)
White
0 Participants
n=99 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=99 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants
Region of Enrollment
United States
15 participants
n=99 Participants
Marital Status
Single
3 Participants
n=99 Participants
Marital Status
Separated/Divorced
3 Participants
n=99 Participants
Marital Status
Married
8 Participants
n=99 Participants
Marital Status
Widowed
1 Participants
n=99 Participants
Employment
Full-time
7 Participants
n=99 Participants
Employment
Part-time
2 Participants
n=99 Participants
Employment
Homemaker
1 Participants
n=99 Participants
Employment
Not employed, retired
5 Participants
n=99 Participants
Relationship to loved one with dementia
Spouse
2 Participants
n=99 Participants
Relationship to loved one with dementia
Daughter
10 Participants
n=99 Participants
Relationship to loved one with dementia
Son
0 Participants
n=99 Participants
Relationship to loved one with dementia
Other relative
0 Participants
n=99 Participants
Relationship to loved one with dementia
Friend/Neighbor
0 Participants
n=99 Participants
Relationship to loved one with dementia
Other
3 Participants
n=99 Participants
Years as caregiver to the loved one with dementia
4.4 years
STANDARD_DEVIATION 3.4 • n=99 Participants

PRIMARY outcome

Timeframe: Baseline and 6 months post baseline

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

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.

Outcome measures

Outcome measures
Measure
Peer Support
n=15 Participants
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.
Medical Outcomes Study Social Support Survey (MOS SSS)
Emotional/Informational Support at Baseline
3.75 score on a scale
Standard Deviation 1.03
Medical Outcomes Study Social Support Survey (MOS SSS)
Emotional/Informational Support at 6 Months
3.79 score on a scale
Standard Deviation 0.99
Medical Outcomes Study Social Support Survey (MOS SSS)
Tangible support at Baseline
3.68 score on a scale
Standard Deviation 1.02
Medical Outcomes Study Social Support Survey (MOS SSS)
Tangible support at 6 months
3.50 score on a scale
Standard Deviation 1.29
Medical Outcomes Study Social Support Survey (MOS SSS)
Affectionate support at Baseline
4.22 score on a scale
Standard Deviation 0.67
Medical Outcomes Study Social Support Survey (MOS SSS)
Affectionate support at 6 months
3.95 score on a scale
Standard Deviation 0.90
Medical Outcomes Study Social Support Survey (MOS SSS)
Positive social interaction at Baseline
4.11 score on a scale
Standard Deviation 0.72
Medical Outcomes Study Social Support Survey (MOS SSS)
Positive social interaction at 6 months
3.98 score on a scale
Standard Deviation 0.83
Medical Outcomes Study Social Support Survey (MOS SSS)
Overall social support at Baseline
3.88 score on a scale
Standard Deviation 0.75
Medical Outcomes Study Social Support Survey (MOS SSS)
Overall social support at 6 months
3.77 score on a scale
Standard Deviation 0.83

Adverse Events

Peer Support

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Karen O. Moss

Ohio State University

Phone: (614) 688-3100

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place