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

NCT06443164 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2025-07-31

No results posted yet for this study

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.

Conditions

  • Pain Catastrophizing
  • Pain, Chronic
  • Gender Identity

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.

Sponsors & Collaborators

  • Oregon Health and Science University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-15
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • United States

Study Locations

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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 NCT06443164 on ClinicalTrials.gov