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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05140174
Other study ID # 2021-1133
Secondary ID A171600Protocol
Status Completed
Phase N/A
First received
Last updated
Start date January 14, 2022
Est. completion date August 10, 2023

Study information

Verified date August 2023
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The proposed research will use a community-based participatory research (CBPR) approach to engage with community organizations to design and implement a project that trains therapists to provide effective, supportive, and engaged therapy to two-spirit, transgender, and nonbinary (2STNB) clients most impacted by barriers in accessing mental health care. 10 2STNB licensed mental health therapists will be identified and 50 2STNB of their clients will be enrolled and can expect to be on study for 10-20 months.


Description:

The long-term aim of this research is to ensure that therapists have access to training and engage in effective psychotherapy that ultimately reaches Two-spirit, transgender, and nonbinary (2STNB) clients who are the most impacted by unequal systems that create mental health concerns. To make real improvement in reaching TNB populations who lack the most access to mental health care, therapists must be properly trained and data from clients about their mental health experiences must be obtained. The proposed research will use a community-based participatory research (CBPR) approach to engage with community organizations to design and implement a project that trains therapists to provide effective, supportive, and engaged therapy to TNB clients most impacted by barriers in accessing mental health care. Intervention: - Therapist Training: The Radical Healing and Internalized Stigma (RHIS) training provides education to therapists on radical healing and internalized stress. The ten therapists employed by the study will engage in an 8 hour intensive training by consultants hired to be on this study. - Participants: - T0 - baseline surveys - T1a to T1p - psychotherapy sessions (session complete within 11 months) - T2 - end intervention surveys - T3 - post intervention follow up (up to 6 months post intervention) Aim 1: Determine best methods for recruiting 2STNB clients (e.g., increasing access to care), with attention to specific populations and barriers (BIPOC, lack of trust, finances, identity match, etc.) Aim 2: Examine the feasibility/acceptability of a specialized training for therapists that focuses on healing and internalized stigma Aim 3: Longitudinally investigate the impact of access to mental health care (e-therapy) on 2STNB people's well-being/mental health. Endpoints: The primary endpoint of the study is to determine if the study actually improved access to mental health care for study participants--this will be determined through qualitative interviewing. An additional endpoint is determining feasibility/acceptability of the study, which will also be assessed via qualitative methods. A secondary endpoint for this study will be to determine if clients experienced psychological improvement in their mental health over the course of the study.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date August 10, 2023
Est. primary completion date August 10, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - fluent in written and spoken English and/or Spanish - willingness to participate in pre/ post/ session-by session assessments and 15 individual psychotherapy treatment sessions - individual identifies as transgender, Two-Spirit, or nonbinary (or somewhere along the gender minority spectrum) - individual identifies as Black, Indigenous/Native, or otherwise as a person of color - not currently in individual therapy with another therapist Exclusion Criteria: - reports current, unmanaged serious/persistent mental health symptoms requiring inpatient treatment (e.g., hallucinations, delusions) - individual does not identify as transgender, Two-Spirit, or nonbinary (or somewhere along the gender minority spectrum) - currently in therapy with an individual therapist

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Radical Healing and Internalized Stigma (RHIS) Training
8-hour RHIS training includes, readings that discuss radical healing and internalized stigma, access to didactic information regarding radical healing and internalized stigma. Therapists will role play certain scenarios that may involve minority stress experiences and discuss with the trainers different types of responses that could be therapeutic. The training will focus on the most up to date research regarding transgender mental health, minority stress, radical healing, and role-plays that focus on these processes.

Locations

Country Name City State
United States University of Wisconsin Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants who Find the Intervention Acceptable Acceptability of the Intervention will be assessed qualitatively via semi-structured interviews post intervention. up to 20 months
Primary Number of Participants Who Find Intervention Feasible Feasibility of the Intervention will be assessed qualitatively via semi-structured interviews post intervention. up to 20 months
Primary Number of Participants Who Indicate Barriers to Therapy Were Decreased Participant Satisfaction with RHIS Intervention will be assessed qualitatively by semi-structured interview with researcher where access to mental health will be queried. up to 20 months
Secondary Change in Percent "Yes" on Yes/No subscales on Gender Minority Stress and Resilience Measure (GMSR) Designed for use with transgender, nonbinary, and gender nonconforming people, the GMSR measure is one of the few that assesses gender identity-related constructs. It was designed to take into account unique gender minority stressors, such as internalized transphobia, and concealment of identity, and resilience factors including community connectedness and pride. The first 3 sub-scales for gender-related discrimination, gender-related rejection, and gender-related victimization are yes/no responses, where 'yes' responses indicated gender-related discrimination, rejection, and victimization. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Gender Minority Stress and Resilience Measure (GMSR) Scores Designed for use with transgender, nonbinary, and gender nonconforming people, the GMSR measure is one of the few that assesses gender identity-related constructs. It was designed to take into account unique gender minority stressors, such as internalized transphobia, and concealment of identity, and resilience factors including community connectedness and pride. The last sub-scales are given on a 5-point Likert response scale (Strongly Disagree = 0 to Strongly Agree = 4) and responses are summed. Higher scores are indicative of greater phenomena. Sub-scales are as follows:
Non-Affirmation: 6-items (0-24)
Internalized Transphobia: 8-items (0-32)
Pride: 8-items (0-32)
Negative Expectations for Future Events: 9-items (0-36)
Non-Disclosure: 5-items (0-20)
Community Connectedness: 5-items (0-20)
baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Outcome Questionnaire-45 (OQ-45) Score The OQ-45 is a measure of how a person has felt in the past week. Total possible range of scores from 0-180, where the higher the score, the more disturbed the participant. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Depression, Anxiety, and Stress Scale (DASS) Scores The DASS is a measure of how perceived depression, anxiety, and stress in the past week. Total possible range of scores for each domain is 0-21, where higher scores indicate more severe depression, anxiety, and stress. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Coping with Discrimination Scale (CDS) Score CDS is a 25-item scale measuring five specific strategies (i.e., education/advocacy, internalization, drug and alcohol use, resistance, and detachment) that minority individuals may use when coping with experiences of prejudice and discrimination. Items are responded to on a 6-point Likert-type scale ranging from 1 = never like me to 6 = always like me, for a range of 25 - 150. The investigators will analyze a longitudinal change through time, where better coping is evidenced by higher scores. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Schwartz Outcome Scale Score This is a 10-item measure of how someone feels over the previous 7 days. Total possible range of scores is 0-100 where higher scores indicate improved outcome. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
Secondary Change in Client Task Specific Change Measure This is a 16-item measure of how someone feels they've changed. Total possible range of scores is 16-112, where higher scores indicate improved outcome. baseline, post-intervention (up to 14 months), follow-up (up to 20 months)
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