Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
FEMALE
ID05436106

Behavioral Intervention to Reduce Psychological Distress Symptoms Among Black Gender Minority Women Experiencing Chronic Stigma

Led by Emory University · Updated on 2026-01-30

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

E

Emory University

Lead Sponsor

N

National Institute of Nursing Research (NINR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are developing and testing a community-based behavioral intervention designed to reduce psychological distress symptoms, such as post-traumatic stress and depression, caused by chronic stigma among Black transgender women. This study aims to create a culturally informed program with input from community members through focus groups and theater testing. The trial will evaluate the feasibility and preliminary effects of this intervention in helping participants manage psychological distress related to stigma exposure. The intervention uses an adaptive approach with seven module-based sessions chosen based on participant feedback. It combines weekly group sessions co-led by a community expert and a public health nurse with supplemental educational materials accessible online through a portal or app. Participants will also have access to social resources via the same online platform. The trial includes both in-person sessions in Atlanta, GA, and online sessions via Zoom, delivered over up to 12 weeks. Participants will be involved in multiple assessments, including surveys at baseline, mid-intervention (3-6 weeks), immediately post-intervention, and three months after completion. Researchers will track intervention retention, attendance, acceptability, accessibility, and fidelity to the program. Changes in psychological distress, including PTSD symptoms and depression scores, will also be measured. The study will monitor recruitment and retention rates, as well as participant engagement with the intervention content.

CONDITIONS

Brief Title

Behavioral Intervention to Reduce Stress Among Black Gender Minority Women

Who Can Participate

Age: 18Years - 99Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Gender is woman, transgender feminine, or female
  • Assigned male sex at birth
  • Speak and read English
Not Eligible

You will not qualify if you...

  • Enrolled in mental health treatment or a controlled consequential environment (e.g., mental health transitional living environment)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual)

Treatment

Duration - Up to 12 weeks

Participants attend a 7-session behavioral intervention with weekly group sessions co-led by a community member and a public health nurse, supplemented by educational content and social resources accessible online.

Weekly group sessions with 3 in-person sessions in Atlanta and 4 online sessions via Zoom

Follow-up

Duration - 3 months post-intervention

Participants complete assessments at mid-intervention, immediately post-intervention, and 3 months post-intervention to evaluate outcomes and intervention acceptability.

4 assessment time points via self-administered surveys on internet-accessible devices

Trial Site Locations

Total: 1 location

1

Emory University School of Nursing

Atlanta, Georgia, United States, 30322

Actively Recruiting

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Research Team

A

Athena DF Sherman, PhD, PHN, RN

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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