- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06614868
Minority Stress Counseling for LGBTQ+ Individuals (MST)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adult participants will respond to advertisements by emailing a research assistant.
A research assistant will then arrange for a pre-screening interview to ensure inclusion criteria are met.
A research assistant will review informed consent and receive a signed informed consent during the pre-screening.
Participants who are accepted into the study will then be offered up to 12 sessions of ACT or receive an unstructured treatment as usual counseling condition delivered by graduate students in the UAB medical/clinical psychology program under the supervision of Dr. Borgogna. These sessions will be 45 minutes each and delivered in Dr. Borgogna's lab. During the first sessions a survey battery will be administered on a lab secure computer administered via Qualtrics. It will be re-administered at session six, and during the last session.
The survey will include a broad base of demographic, mental health, and minority stress measures.
Participants will be assigned a random number that will link their survey responses across sessions. Identifying information will not be gathered as part of data collection.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Nicholas Borgogna (Assistant Professor), PhD
- Phone Number: 7579693677
- Email: borgogna@uab.edu
Study Locations
-
-
Alabama
-
Birmingham, Alabama, United States, 35294
- Recruiting
- University of Alabama at Birmingham
-
Contact:
- Nicholas Borgogna, PhD
- Phone Number: 435258961
- Email: borgogna@uab.edu
-
Contact:
- Nicholas Borgogna
-
Principal Investigator:
- Nicholas Borgogna, PhQ
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Must identify as non-heterosexual
Exclusion Criteria:
Suicide attempt within the past 12 months.
Current eating disorder.
Narcotics use within the past 3 months
Non-suicidal self-injury within the past 6 months.
Current/History of psychosis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group
Participants receiving acceptance and commitment therapy
|
Up to 16 session of unstructured counseling therapy informed by Acceptance and Commitment Therapy tradition.
|
|
Active Comparator: Treatment as usual
Unstructured counseling intervention
|
Unstructured counseling
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Alcohol Problems
Time Frame: 16 Weeks
|
Alcohol Use Disorders Identification Test
|
16 Weeks
|
|
Depression
Time Frame: 12 weeks
|
Patient Health Questionnaire-9
|
12 weeks
|
|
Anxiety
Time Frame: 12 Weeks
|
Generalized Anxiety Disorder-7
|
12 Weeks
|
|
Post Traumatic Stress
Time Frame: 12 Weeks
|
Patient Checklist-5
|
12 Weeks
|
|
Internalized Heterosexism
Time Frame: 12 Weeks
|
Internalized Homophobia Scale
|
12 Weeks
|
|
Discrimination
Time Frame: 12 Weeks
|
Daily Heterosexist Questionnaire
|
12 Weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Experiential Avoidance
Time Frame: 16 Weeks
|
Experiential Avoidance Rating Scale
|
16 Weeks
|
|
Affect
Time Frame: 16 Weeks
|
Positive Negative Affect Schedule
|
16 Weeks
|
|
Problematic Pornography Use
Time Frame: 12 Weeks
|
Brief Pornography Screen
|
12 Weeks
|
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
Other Study ID Numbers
- IRB-300013570
- NBLAB1 (Other Identifier: UAB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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