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ENROLLING BY INVITATION
NCT06443164
NA

Efficacy of a Chronic Pain Treatment Prior to Gender-affirming Surgery

Sponsor: Oregon Health and Science University

View on ClinicalTrials.gov

Summary

The primary objective of this study is to examine a single-session, 2-hour group intervention provided to a population of transgender or gender-diverse patients with chronic pain prior to gender-affirming surgery, to determine if participants who receive the intervention have less pain-related distress compared to participants randomly assigned to the control group.

Official title: Efficacy of a Single-session Treatment for Reducing Chronic Pain Prior to Gender-affirming Surgery

Key Details

Gender

All

Age Range

18 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

78

Start Date

2024-05-15

Completion Date

2025-12-31

Last Updated

2025-07-31

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Empowered Relief

Pain Management Course that has been used to treat pain in patients with different pain conditions.

OTHER

Standard of Care

Gender Affirming surgery without any attention to pain conditions prior to surgery.

Locations (1)

OHSU Comprehensive Pain Center

Portland, Oregon, United States