SGM Evidenced-Based Mental Healthcare Implementation

NCT05890404 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1410

Last updated 2025-08-05

No results posted yet for this study

Summary

The purpose of the proposed study is to identify effective strategies for implementing lesbian, gay, bisexual, transgender, and queer (LGBTQ)- affirmative Cognitive-Behavioral Therapy (CBT) at LGBTQ community centers across the United States.

Conditions

  • CBT
  • LGBTQ

Interventions

BEHAVIORAL

LGBTQ-Affirmative CBT Training: Materials Only

Participants will be provided a digital suite of online self-guided learning materials, including step-by-step treatment materials, client handouts, and "how to" instructions for delivering the treatment.

BEHAVIORAL

LGBTQ-Affirmative CBT Training: Direct Training

Participants will be provided a digital suite of online self-guided learning materials, including step-by-step treatment materials, client handouts, and "how to" instructions for delivering the treatment. In addition, participants will receive 12 weekly 1-hour live training webinars on delivering LGBTQ-affirmative CBT led by expert trainers.

BEHAVIORAL

LGBTQ-Affirmative CBT Training: Local Supervision

Participants will be provided a digital suite of online self-guided learning materials, including step-by-step treatment materials, client handouts, and "how to" instructions for delivering the treatment. In addition, participants will receive 12 weekly 1-hour live training webinars on delivering LGBTQ-affirmative CBT led by expert trainers. This arm will also receive one year of ongoing (at least monthly) supervision in LGBTQ-affirmative CBT from an expert supervisor at your center.

Sponsors & Collaborators

  • Northwestern University

    collaborator OTHER
  • Arizona State University

    collaborator OTHER
  • Miami University

    collaborator OTHER
  • University of Miami

    collaborator OTHER
  • CenterLink

    collaborator UNKNOWN
  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • Yale University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-08
Primary Completion
2027-10-01
Completion
2028-06-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05890404 on ClinicalTrials.gov