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NCT04856462 | NOT YET RECRUITING | Stress, Psychological


Culturally Responsive Caregiver Support
Sponsor:

University of Michigan

Information provided by (Responsible Party):

Law Robinson-Lane

Brief Summary:

Black family caregivers of older adults with Alzheimer's disease and/or related dementias (ADRD), have an increased mortality risk related to pre-existing health conditions and stress. Targeted, culturally responsive, health interventions that help Black ADRD caregivers to effectively manage their own health and use community preferenced ways of coping, can improve caregivers' overall health, perceived ability to provide care for a person with ADRD (self-efficacy), and increases the likelihood that they will experience benefits from caregiving. This clinical trial pilot will test the feasibility of a community based intervention designed to improve health outcomes for Black family caregivers of persons with ADRD.

Condition or disease

Stress, Psychological

Adaptation, Psychological

Intervention/treatment

Education Support

Phone Call

Phase

NA

Detailed Description:

The proposed intervention is a telephonically-based support program that will follow a peer supportive model to engage small groups of caregivers over 12 weeks. During each week of the intervention, participants (n = 36, 4/ group) will engage in a small facilitator lead, support group. Each week, caregivers will be provided with a different culturally relevant caregiving or personal health strategy to practice. During the weekly support calls, a facilitator will provide an overview of the content covered and each participant will have the opportunity to discuss their past week and how they engaged the weekly strategy or found barriers to it. The format will be structured enough to ensure that content is covered and everyone is able to be equally engaged while flexible enough that caregivers can receive support in the areas they need. A battery of assessment measures will be taken prior to the start of the intervention, halfway through at 6 weeks, at 12 weeks, 30 days following the intervention, and then 6 months following the intervention.

Study Type : INTERVENTIONAL
Estimated Enrollment : 36 participants
Masking : DOUBLE
Masking Description : Participants and group facilitators in the control group will made aware that they are part of the control gropu
Primary Purpose : SUPPORTIVE_CARE
Official Title : Culturally Responsive Support Programming for Black Caregivers of Persons with Dementia
Actual Study Start Date : 2024-12-01
Estimated Primary Completion Date : 2025-05-30
Estimated Study Completion Date : 2025-05-30

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 55 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: 1
Criteria
Inclusion Criteria
  • 1. Self-identified as Black/ African American
  • 2. At least 55 years old
  • 3. Able to speak and understand English
  • 4. Related to, or has a close personal relationship to a person over the age of 55 that has an ADRD diagnosis or evidence of cognitive impairment
  • 5. Is responsible for, monitors, and/ or provides assistance in activities of daily living for the care recipient as a family/friend unpaid responsibility
  • 6. Score of 14 or higher on the Animal Naming Test.
  • 7. Able to adequately hear by phone to engage with the group
Exclusion Criteria: Caregivers will be excluded from the study if they do not meet the inclusion criteria, decline to participate for any reason, or do not give consent for participation
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  • Culturally Responsive Caregiver Support

    Location Details

    NCT04856462


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