Survey Experiment to Estimate Level of Mental Illness Stigma Based on Condition and Gender

June 7, 2024 updated by: Yale University

Measuring Level of Mental Illness Stigma Based on Condition and Gender

This study aims to measure levels of mental illness stigma based on condition and gender of the participants and individual portrayed with mental illness.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This study aims to measure levels of mental illness stigma based on condition and gender of the participants and individual portrayed with mental illness. This study utilizes eight vignettes portraying different mental illnesses and genders to measure the levels of mental illness stigma in the general community in rural Uganda.

Study Type

Interventional

Enrollment (Actual)

379

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Iganga, Uganda
        • Empowerment to Heal - Uganda

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • All adults who consider Buyende District their primary residence and who are capable of providing consent

Exclusion Criteria:

  • Minors younger than 18 years of age
  • Persons who do not consider Buyende District their primary place of residence

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: V1: Woman with Major Depressive Disorder
Depicting a young woman with symptomatic major depressive disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V2: Man with Major Depressive Disorder
Depicting a young man with symptomatic major depressive disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V3: Man with Generalized Anxiety Disorder
Depicting a young man with symptomatic generalized anxiety disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V4: Woman with Generalized Anxiety Disorder
Depicting a young woman with symptomatic generalized anxiety disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V5: Woman with Schizophrenia
Depicting a young woman with symptomatic schizophrenia
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V6: Man with Schizophrenia
Depicting a young man with symptomatic schizophrenia
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V7: Woman with Alcohol Use Disorder
Depicting a young woman with symptomatic alcohol use disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.
Experimental: Experimental: V8: Man with Alcohol Use Disorder
Depicting a young man with symptomatic alcohol use disorder
The intervention is being assigned to one of the 8 different versions of the survey vignette.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Level of acceptance for the individual depicted in the vignette as measured by PERSONAL ACCEPTANCE SCALE
Time Frame: Study period. For each interview, approximately 60 minutes.
The PAS is a 9-item questionnaire targeted to public stigma, the "negative attitudes, beliefs, and behaviors held within a community" against individuals with mental illness. Each yes adds one point to the scale, and five questions from each scale were reverse-scored to match the direction of the scale. The total number of points was divided by the number of questions (nine) and multiplied by ten to generate numbers between zero and ten for comparison purposes to the Broad Acceptance Scale. Higher scores indicated more acceptance and less stigma towards mental illness, while lower scores indicated less acceptance and more stigma towards mental illness.
Study period. For each interview, approximately 60 minutes.
Level of acceptance for the individual depicted in the vignette as measured by BROAD ACCEPTANCE SCALE
Time Frame: Study period. For each interview, approximately 60 minutes.
The BAS is a 9-item questionnaire targeted to structural stigma, the "societal-level conditions, cultural norms, and institutional practices that constrain the opportunities, resources, and wellbeing" for individuals with mental illness. Each yes adds one point to the scale, and five questions from each scale were reverse-scored to match the direction of the scale. There were ten questions, therefore it generated a score between zero and ten. Higher scores indicated more acceptance and less stigma towards mental illness, while lower scores indicated less acceptance and more stigma towards mental illness.
Study period. For each interview, approximately 60 minutes.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 15, 2023

Primary Completion (Actual)

September 15, 2023

Study Completion (Actual)

September 15, 2023

Study Registration Dates

First Submitted

February 14, 2024

First Submitted That Met QC Criteria

February 19, 2024

First Posted (Actual)

February 28, 2024

Study Record Updates

Last Update Posted (Actual)

June 10, 2024

Last Update Submitted That Met QC Criteria

June 7, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2000034605_a

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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