Encouraging Cognitive Screenings at African American Churches

Sponsor
University of Kansas Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT05037578
Collaborator
University of Missouri, Kansas City (Other)
100
1
2
24
4.2

Study Details

Study Description

Brief Summary

This pilot study plans to examine feasibility and outcomes of a culturally/religiously-tailored church-based dementia screening intervention among older adult African American church members and community members who use church outreach services in 4 African American churches.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Project Grace
Phase 1

Detailed Description

The primary aim of this study is to conduct an exploratory pilot study to examine feasibility and outcomes of a culturally/religiously-tailored church-based dementia screening intervention among older adult African American church members and community members who use church outreach services in 4 African American churches (N=100). Our secondary outcomes are to assess the impact of the intervention on dementia-related stigma and linkage to care. Intervention content is based on the Theory of Planned Behavior; intervention delivery is based on the Social-Ecological Model - both guided by a faith community engagement approach. Trained faith leaders will deliver the tailored intervention through multilevel church outlets: individual self-help resources (e.g., risk checklist, commitment to screening cards); group ministry discussion guides/seminar on dementia; church-wide services using sermon guides, responsive readings, and church bulletin inserts; and church-community level text messages, dementia screening, and linkage to care services. Two screening events will be held at each church. We will also conduct a process evaluation that will include post-test study focus groups.

Specific Aim 1. Test a religiously/culturally-tailored, church-based dementia screening intervention on receipt of dementia screening, stigma, and LTC use among an older adult African American church-populations at 4 months.

Hypothesis. The tailored church-based dementia screening intervention will evidence increased screening and LTC rates, and lower dementia-related stigma beliefs at 4 months.

Specific Aim 2. Evaluate predictors of receipt of dementia screening at 4 months among older adult African American church-populations to determine modifiable screening facilitators/barriers.

Specific Aim 3. Conduct a process evaluation to examine study intervention implementation facilitators, barriers, and dose along with exposure and satisfaction to identify essential intervention components.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
A Church-based Intervention for Increasing Screening for Dementia Among African American Older Adults (ADC Pilot): Project Grace
Actual Study Start Date :
Jul 1, 2019
Actual Primary Completion Date :
Jun 19, 2021
Actual Study Completion Date :
Jun 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Project Grace

This intervention will be delivered through church-based multilevel activities by trained church leaders using religiously/ culturally-tailored study materials (sermon guides, responsive readings, educational games, brochures, educational/testimonial videos) packaged in a culturally-tailored. Intervention churches will receive the Project Grace Tool Kit and intervention implementation directions to seek cognitive screening. These churches will hold a Project Grace Kickoff event, where a sermon, and other tool kit materials will be distributed. After the Kick-off, liaisons will deliver 1-2 Tool Kit materials/activities per month through targeted multilevel church activities over 4 months. Delivery of intervention components will coincide with existing, multilevel activities that occur in churches through: a) churchwide services, b) outreach ministry groups; and c) individual level activities (e.g., text/voice/email health promotion messages from church) over 4 months.

Behavioral: Project Grace
A multilevel church-based intervention to encourage cognitive screens and brain health.

Active Comparator: Standard Control

Standard information churches will receive standard dementia education information. These churches will receive: a) non-tailored project materials collected from mental health organizations and b) standard community-based mental health screening events) coordinated by their Community Health Liaisons. These churches will receive all Project Grace Tool Kit materials and implementation training after the completion of assessments.

Behavioral: Project Grace
A multilevel church-based intervention to encourage cognitive screens and brain health.

Outcome Measures

Primary Outcome Measures

  1. Number of Participants who received a cognitive screening [4 months from baseline]

    Question at 4 months from baseline asking whether the participant has received a cognitive screening within the last 4 months

  2. Number of Participants who were linked to care services [4 months from baseline]

    Question at 4 months from baseline asking whether the participant has received a linkage to care services within the last 4 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Age ≥55

  2. Regular church member (attending church > monthly) or community member receiving church outreach services (>3 times annually)

  3. Willing to participate in two surveys (baseline and 4 months)

  4. Willing to provide contact information for at least 2 other persons

  5. Residing in the Kansas City metropolitan area

  6. Provide a working contact email address or number

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 School of Medicine, UMKC Kansas City Missouri United States 64108

Sponsors and Collaborators

  • University of Kansas Medical Center
  • University of Missouri, Kansas City

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Kansas Medical Center
ClinicalTrials.gov Identifier:
NCT05037578
Other Study ID Numbers:
  • 2017382 KC
First Posted:
Sep 8, 2021
Last Update Posted:
Sep 16, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2021