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DECIDE: Dyads and Families

StatusWithdrawn
PhaseNot applicable
Started2022-07-15
View on ClinicalTrials.gov ↗
Why the trial stopped
No participants were enrolled in the clinical trial portion. The community-engaged nature of the project required more time than anticipated, and funding was insufficient to support the implementation of the proposed intervention.

Amendment history

2026-09-19
Trial status changed: Enrolling by Invitation → Withdrawn
Trial withdrawn: No participants were enrolled in the clinical trial portion. The community-engaged nature of the project required more t...
2026-07-16
Recruiting→Enrolling by Invitation Study Identification, Study Status, Oversight, Contacts/Locations v10
Trial statusRecruiting→Enrolling by Invitation
Primary completion date2026-12→2027-08-31
Completion date2026-12→2027-08-31
Study sitesdetails revised at 4 of 4 sites
2025-06-30
2 amendments v8-v9
2 re-verifications since 2024-06-21, no change to tracked fields
2023-06-02
Study Status, Study Description, Eligibility v7
Eligibility criteria+239 characters
[...] isease and related dementias(PLWD): Inclusion Criteria: self-identifies as African American age 50 years or older communi [...] imer's Association clinical criteria for probable (Alzheimer's Disease (AD) able to read, speak, and understand English wi [...] r (e.g., schizophrenia). Caregiver: Inclusion Criteria: self-identifies as African American 18 years of age or older daug [...] for caregiver except not actively providing care because of the death of their parent or the parent has been transitioned t [...] he parent should be at least 12 months prior to recruitment. Caregiver of persons with severe dementia Inclusion [...]
Study description+204 characters
[...] the phone number, email address of the research team, and a quick response (QR) code for potential participants to contact the research tea [...] hose parent(s) have died or are in long-term care facilities and adult daughters caring for a parent with severe dementia only. For past adult daughter caregivers whose parents have died [...] articipants will be key informants who participate in focus groupsgroup sessions using design thinking strategies to develop the pr [...] . Key informants will consist of parent-adult daughter dyads and, past adult daughter caregivers, and adult daughter caregivers of persons with [...] [...]
2022-07-18
Study Status v6
Start dateestimated 2022-06→confirmed 2022-07-15
Show 5 earlier versions
2022-06-14
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v5
Trial statusNot Yet Recruiting→Recruiting
Start date2022-05→2022-06
Study sitesdetails revised at 4 of 4 sites
2022-05-19
Study Status, Outcome Measures v4
Primary endpoints7 to 5 entries
Change in number of health care provider visits Change in number of hospitalizations
2022-04-25
Study Status, Outcome Measures, Contacts/Locations v3
Start date2022-04→2022-05
Study sites0→4
Primary endpoints6 to 7 entries
Change in Decision Self-Efficacy Scale Score
2022-03-07
Study Status v2
Start date2022-02→2022-04
2022-02-08
Study Status, Outcome Measures, Eligibility v1
Start date2024-12→2022-02
Eligibility criteria-1 characters
[...] as African American age 50 years or older community-dwelling; experiencing signs and symptoms of mild to moderate dementi [...]
Primary endpoints4 to 6 entries
Change in number of health care provider visits Change in number of hospitalizations
2021-11-17
Original filing
Emory University
371 trials monitored
See 23 trials at risk
Alzheimer's Disease
1,140 trials monitored
See 62 trials at risk
Dementia
912 trials monitored
See 44 trials at risk
The purpose of this study is to design and test a decision-making program that is tailored to support adult daughters making healthcare decisions for their parents who are living with memory loss to improve the quality of life of African American families. There are two phases of this research study. The first phase will collect information by surveys and/or interviews. The surveys and interviews will ask questions about demographics (e.g., age, race/ethnicity), culture, health, family dynamics, caregiving, and healthcare experiences. The surveys will be completed by all eligible adult daughters and parents with memory loss in pairs. The interviews will be completed by a smaller number of pairs and by all former adult daughter caregivers. The general scope of topics is caregiving experiences, cultural identity, healthcare decisions for persons living with Alzheimer's disease, and related dementias, health, and well-being. The research team will identify and examine key factors that will lead to designing and testing the feasibility of a culturally tailored prototype intervention for African American dementia dyads/families of persons living with mild to moderate Alzheimer's disease and related dementias.
Trial Details
NCT Number NCT05139290
Lead Sponsor Emory University
Collaborators: National Institute on Aging (NIA)
Conditions Dementia, Alzheimer Disease, Caregiver Burden
Start Date 2022-07-15
Primary Completion 2027-08-31 (estimated)
Study Completion 2027-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-09-18