Ignite Creation Date:
2024-05-06 @ 4:03 PM
Last Modification Date:
2024-10-26 @ 2:02 PM
Study NCT ID:
NCT04856462
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-06
First Post:
2021-04-19
Brief Title:
Culturally Responsive Caregiver Support
Sponsor:
University of Michigan
Organization:
University of Michigan
Study Overview
Official Title:
Culturally Responsive Support Programming for Black Caregivers of Persons With Dementia
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Black family caregivers of older adults with Alzheimers disease andor 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
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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None