Peer Support for Family Caregivers of Older Adults Living With Dementia

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorOhio State University

About this trial

Family caregivers of people living with dementia are at high risk of poor health when caregiving for their loved one. Peer Support for Family Caregivers of Older Adults Living with Dementia (Pair 2 Care©) is a simple, nonjudgmental, flexible, and potentially scalable peer support program developed with and for family caregivers along with former (previous) caregivers, community leaders, and healthcare providers. Using the experiences of trained former caregivers as mentors to current caregiver mentees, Pair 2 Care© may lower caregiver depressive symptoms and promote health and well-being of current caregivers, their loved ones, and former caregivers while informing future Alzheimer's disease and Alzheimer's disease-related dementia caregiving policy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

English-speaking

Adult (18+)

Family Caregivers of people living with dementia (current or former)

Disqualifiers

Non-English-speaking

Under age 18

Non-family caregiver

Trial design

Design model

Crossover

Treatments tested in this trial

  • Peer Support

    Behavioral

    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.

  • Usual Care

    Behavioral

    Will include AD/ADRD and caregiving literature, as the control condition because it will provide a more real-world comparison. After completing the Month 6 data collection, they will be offered the Pair 2 Care intervention.

Treatment groups

344 Participants
are divided into 2 treatment groups
Group A: Peer SupportExperimental treatment 1 intervention
Group B: Active ControlActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Center for Epidemiologic Studies Depression Scale Revised (CESD-R-10)

The Center for Epidemiologic Studies Depression Scale Revised (CESD-R-10) will be used to measure depressive symptoms.74 The CESD-R-10 is reliable (Cronbach's α = .86) and valid (convergent = .91; divergent = .89).

Time frame
Baseline, 3 months, 6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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Ohio State University

Lead sponsor

National Institute on Aging (NIA)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: