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Behavioral Intervention

Inclusionary Practices for Mental Illness

N/A
Recruiting
Research Sponsored by Temple University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to test a behavioral intervention in faith communities to increase inclusivity towards individuals with serious mental illness. The study will determine if the intervention leads to more inclusive practices, greater understanding of mental illness

Who is the study for?
This trial is for faith communities interested in becoming more inclusive towards individuals with serious mental illness. Congregations must be willing to form an inclusion committee, participate in a half-day training on mental health and inclusion, and engage in surveys about their practices.
What is being tested?
The study tests if a behavior-based intervention can increase welcoming practices within faith communities. It involves forming committees, training members on mental health awareness, and altering congregational habits to support people with serious mental illnesses better.
What are the potential side effects?
There are no traditional medical side effects as this is a behavioral intervention study. However, participants may experience changes in community dynamics or face challenges adapting new inclusive practices.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
This trial's timeline: 3 weeks for screening, Varies for treatment, and survey will be administered 2 times at the baseline and 11-12 months later at the end of the study for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Community Attitudes Toward the Mentally Ill
Inclusionary practices
Indicators of Welcome
+4 more
Secondary study objectives
Lerman Quality of Life Interview
University of California Los Angeles Loneliness Scale

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Behavior intervention to increase inclusionary practicesExperimental Treatment1 Intervention
Each congregation will participate in the intervention for 11-12 months

Find a Location

Who is running the clinical trial?

Temple UniversityLead Sponsor
316 Previous Clinical Trials
88,607 Total Patients Enrolled
National Institute on Disability, Independent Living, and Rehabilitation ResearchFED
80 Previous Clinical Trials
9,437 Total Patients Enrolled
~350 spots leftby Dec 2025