Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06292637

Cognitive Behavioral and Faith Fellowship to Improve Thy Health

Led by University of Wisconsin, Madison · Updated on 2025-09-30

50

Participants Needed

3

Research Sites

99 weeks

Total Duration

On this page

Sponsors

U

University of Wisconsin, Madison

Lead Sponsor

A

Agency for Healthcare Research and Quality (AHRQ)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Investigators will examine the efficacy of a faith-based depression intervention, in reducing symptoms of depression among African American adults in Wisconsin. Twelve church groups, each with 10 people (N=120) will be invited to participate. This intervention will be the first evidence-based, faith-based intervention designed for African Americans if validated.

CONDITIONS

Official Title

Cognitive Behavioral and Faith Fellowship to Improve Thy Health

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-identify as an African American man or woman
  • Age 18 years or older
  • Have symptoms of major depressive disorder with a Patient Health Questionnaire-9 (PHQ-9) score of 10 or higher
Not Eligible

You will not qualify if you...

  • Diagnosis of major psychotic illnesses such as schizophrenia
  • Current participation in psychotherapy
  • Current suicidal thoughts requiring risk assessment and referral
  • Recent changes to psychiatric medications requiring a 4-week stabilization period before enrollment
  • Alcohol or drug dependence unless sober and clean for at least 3 months

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 3 locations

1

University of Wisconsin - Madison

Madison, Wisconsin, United States, 53515

Actively Recruiting

2

Second Baptist Church

Madison, Wisconsin, United States, 53711-3800

Actively Recruiting

3

The Board of Regents of the UW System

Madison, Wisconsin, United States, 53715-1218

Actively Recruiting

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Research Team

E

Earlise Ward, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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