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Feasibility of a Multi-Level School Intervention for LGBTQ Youth

University of Southern California logo

University of Southern California

Status

Completed

Conditions

Sexual Minority Stress Experiences Among LGBTQ Youth

Treatments

Other: Proud & Empowered!

Study type

Interventional

Funder types

Other

Identifiers

NCT04041414
1R21MD013971

Details and patient eligibility

About

The goal of this R21 grant is to test the feasibility of a theoretically informed, LGBTQ-affirming intervention (Proud & Empowered; P&E). Although LGBTQ adolescents experience disparities in behavioral health outcomes compared to their heterosexual peers, interventions are scarce. For example, LGBTQ adolescents are 3 to 4 times more likely to meet criteria for an internalizing disorder and 2 to 5 times more likely to meet criteria for externalizing disorders than their heterosexual peers. Our intervention seeks to address disparate behavioral health problems such as depression, anxiety and trauma symptomology. Our goal will be achieved by completing two specific aims: 1) Assess the feasibility, including recruitment, enrollment, fidelity of service delivery, satisfaction, safety, and retention, of the intervention in a randomized control trial with four schools, 2) Obtain preliminary estimates of intervention effects on key behavioral health symptoms for LGBTQ youth and school climate (norms, attitudes, beliefs, behaviors) at the school level in preparation for a larger efficacy trial. This innovative R21 application brings together a team of nationally recognized minority stress and prevention science experts and responds to a nationally established public health need for research from the Institute of Medicine, the National Institutes of Health, and the National Gay and Lesbian Task Force.

Enrollment

47 patients

Sex

All

Ages

12 to 20 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • LGBTQ student in one of four high schools

Exclusion criteria

  • Not meeting inclusion criteria

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

47 participants in 2 patient groups

Intervention schools
Experimental group
Description:
Schools will be assigned to either intervention or control schools. Students in intervention schools will receive the intervention in semester 1.
Treatment:
Other: Proud & Empowered!
Control schools
Active Comparator group
Description:
Students in control schools will receive no intervention
Treatment:
Other: Proud & Empowered!

Trial documents
2

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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