Cognitive Behavioral Therapy for Coping with Discrimination
Trial Summary
What is the purpose of this trial?
This study consists of a randomized controlled trial of a multi-session cognitive behavior therapy (CBT) group intervention that addresses coping with discrimination and medical mistrust among Black sexual minority men (SMM). Primary intervention objectives include increasing health care engagement and receipt of evidence-based preventive care, as well as better coping and reduced anticipated and internalized stigma, and medical mistrust among intervention participants.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Cognitive Behavioral Therapy Coping Intervention for coping with discrimination?
Research shows that cognitive behavioral therapy (CBT) can effectively change coping styles and reduce psychological symptoms, as seen in studies where CBT methods like relaxation and problem-solving training led to significant symptom reduction. Additionally, CBT has been adapted successfully for various groups, such as low-income African American women, indicating its flexibility and potential effectiveness in diverse contexts.12345
Is Cognitive Behavioral Therapy (CBT) safe for humans?
How is the CBT Coping Intervention treatment different from other treatments for coping with discrimination?
The CBT Coping Intervention is unique because it not only helps individuals manage personal distress from discrimination but also encourages understanding and addressing the root causes of discrimination, which are often systemic. This approach combines personal coping skills with a broader awareness of social injustice, making it distinct from treatments that focus solely on individual coping strategies.1112131415
Research Team
Laura Bogart, PhD
Principal Investigator
RAND
Eligibility Criteria
This trial is for Black sexual minority men over 18, who have had sex with other men in the past two years and will be in Los Angeles County for the next year. Participants must speak English and have been biologically male at birth. Transgender individuals and cisgender women cannot join.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants receive an 8-session cognitive behavior therapy (CBT) group intervention addressing coping with discrimination and medical mistrust
Follow-up
Participants are monitored for healthcare engagement and receipt of preventive care through surveys at 4-, 8-, and 12-months post-baseline
Treatment Details
Interventions
- CBT Coping Intervention
Find a Clinic Near You
Who Is Running the Clinical Trial?
RAND
Lead Sponsor
University of Massachusetts, Boston
Collaborator
APLA Health
Collaborator
University of Southern California
Collaborator