- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06336980
Creating Welcoming Faith Communities for People With Serious Mental Illnesses
Creating Welcoming Faith Communities for Believers With Serious Mental Illnesses: Testing an Environmental, Behavior-Oriented Intervention
The goal of this intervention study is to test a behavioral intervention to increase inclusionary practices toward individuals with serious mental illness in faith communities. The main questions it aims to answer are:
- To determine if the behavior-based intervention leads to an increase in inclusionary practices (e.g., conducting outreach with mental health agencies).
- To determine if the behavior-based intervention is effective in increasing inclusive practices by members and leaders of faith communities.
- To determine if the intervention leads to a greater understand of mental illness and a decrease in stigmatizing beliefs by congregation members.
- To determine if the intervention results in individuals with serious mental illness and their family members reporting less discrimination and increased inclusion.
Congregations will be asked to create an inclusion committee that will then work on developing systems and changing congregational practices to become more inclusive. All congregation members will be invited to a half-day training that will provide information on mental illness and inclusion, and will provide tips and strategies when they encounter situations or behaviors that are less familiar to them. All congregation members will be given the opportunity to participate in a survey about congregational practices.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Crystal Slanzi, PhD
- Email: crystal.slanzi@temple.edu
Study Contact Backup
- Name: Mark Salzer, PhD
- Phone Number: 215-204-7879.
- Email: mark.salzer@temple.edu
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19121
- Recruiting
- Temple Univeristy
-
Contact:
- Crystal Slanzi, PhD
- Email: crystal.slanzi@temple.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- member or attendee of the faith community participating in the training
Exclusion Criteria:
- under the age of 18
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Behavior intervention to increase inclusionary practices
Each congregation will participate in the intervention for 11-12 months
|
Congregational inclusion committees will participate in monthly training meetings for approximately 1 year.
Each month a new inclusion practice will be introduced and then the committee will be asked to implement it in their congregation.
The 11 practice areas are:1) assessing inclusion needs of members, 2) providing opportunities for members with serious mental illness (SMI) to take on roles and responsibilities, 3) creating an inclusion committee, 4) ensuring that members with SMI are welcomed to all events, 5) creating sensory friendly spaces, 6) offer participation opportunities in multiple formats, 7) adopt policies and practices to support inclusion, 8) using inclusive language, 9) ensure that external communications indicate the congregation is welcoming to all, 10) providing support to family members of individuals with SMI, and 11) conducing outreach to mental health support systems.
Goals may vary per congregation based on their current practices, needs, and preferences.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inclusionary practices
Time Frame: Will be measured once per month for the duration of the study up to one year.
|
Researchers will evaluate inclusionary practices done in the congregation (e.g.
create an intake form for new members).
There might be up to 50 different practices.
The number of practices will vary by congregation.
Each practice will measured as being done or not (yes or no).
A greater number of "yes" responses will indicate greater inclusionary practices.
|
Will be measured once per month for the duration of the study up to one year.
|
|
Indicators of Welcome
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These questions are only being given to everyone who took the survey including those who report they do not have a mental illness, those that report that they do, and those that report that they have a family member with a mental illness.
There are 32 statements related to organizational processes and respondent experiences with inclusion in their congregation.
There are an additional three statements specifically for those with family members with mental illness.
The response options are yes, no, and I don't know.
A greater number of "yes" responses would indicate a greater number of inclusionary practices and greater inclusive experiences and "no" or "I don't know" would indicate the opposite.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Mental Health Knowledge Questionnaire
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These questions are only being given to participants who report that they do not mental illness.
It consists of 6 statements related to knowledge about treatments and outcomes for individuals with mental illness.
Response options range from strongly agree (6) to strongly disagree (1) on a 6-point scale.
Stronger agreement or higher scores across statements indicates a higher level of knowledge about mental illness and a stronger disagreement or lower scores indicates less knowledge about mental illness.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Social Distance Scale
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These questions are only being given to participants who report that they do not mental illness.
This measure assesses participants's comfort level in being around people with mental illness.
It was modified to include measures directly related to faith communities (e.g., would you feel comfortable having someone with a serious mental illness as a member of your congregation).
There are 7 questions with response options that vary from strongly disagree (1) to strongly agree (6) on a 6-point scale.
Stronger agreement or higher scores indicate a higher level of comfort with people with mental illness and stronger disagreement or lower scores indicate a lower level of comfort with people with mental illness.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Community Attitudes Toward the Mentally Ill
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These questions are only being given to participants who report that they do not mental illness.
There are 4 statements related to attitudes toward people with mental illness from this measure.
The response options for each statement range from strongly disagree (1) to strongly agree (6) on a 6-point scale.
Stronger agreement or higher scores across all questions indicate more negative attitudes toward those with mentally illness and stronger disagreement or lower scores (1) across all questions indicates more positive attitudes toward those with mental illness.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Reported and Intended Behavior Scale
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These questions are only being given to participants who report that they do not mental illness.
The measure is divided into two parts.
The first 4 questions ask about the participants current experiences with people with mental illness.
Response options include "yes" or "no, or not that I know of".
A greater number of yes responses indicates more experience with individuals with mental illness.
The second part includes 4 questions asking about a person's willingness to include people with mental illnesses in their life.
The response options are from strongly disagree (1) to strongly agree (6) on a 6-point scale with stronger agreement or higher scores on each question indicating a greater willingness to associate with or include or have people with mental illnesses in their life in the future.
Stronger disagreement or lower scores across questions indicates less willingness to associate with or include people with mental illnesses in their lives.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Sense of Belonging Scale
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These 10 questions are only being given to participants who report having a mental illness or a family member with a mental illness.
The questions ask participants the degree to which they feel welcomed and that they belong in a given environment.
For this study that environment was their congregation.
Response options range from strongly agree to strongly disagree on a 6-point scale.
Stronger agreement or higher scores (6) on questions 2, 3, 4, 7, 8, 9 , and 10 and stronger disagreement (1) or lower scores on questions 1, 5, and 6 indicate a greater sense of belonging.
Stronger disagreement (1) or lower scores to questions 2, 3, 4, 7, 8, 9, and 10 and stronger agreement (6) or higher scores to questions 1, 5, and 6 indicate less of a sense of belonging.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
University of California Los Angeles Loneliness Scale
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
These 3 questions are only being given to participants who report having a mental illness.
The questions related to how often participants feel socially isolated or lonely.
Response options range from 1) hardly ever, 2) some of the time, and 3) often.
Responses (3) indicate increased loneliness and more "hardly ever" responses indicate less loneliness.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
|
Lerman Quality of Life Interview
Time Frame: Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
This measure is only presented to people who report having a mental illness.
Only the first question from this scale is being asked as it correlates well to other items on the interview related to overall quality of life.
The one question asks participants "how do you feel about your life in general?"
Response options vary from terrible to delighted on a 7-point scale.
Responses closer to 7 (delighted) indicate greater perceived quality of life and responses closer to 1 (terrible) indicate lower perceived quality of life.
|
Survey will be administered 2 times at the baseline and 11-12 months later at the end of the study
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 31021
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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