RecruitingNot ApplicableNCT07324967

A Standardized Counseling Approach to Preoperative Education in Transmasculine Individuals Receiving Gender-affirming Surgery


Sponsor

University of Minnesota

Enrollment

250 participants

Start Date

Mar 12, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The intervention will be an educational handout provided to a randomized cohort of patients that reviews the benefits and risks of retaining ovaries vs removing them. This educational handout will be provided prior to the surgical consultation at the time of the initial survey.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is examining whether providing a detailed educational handout before surgery helps transgender and non-binary individuals make more informed decisions about whether to keep or remove their ovaries during a gender-affirming hysterectomy. Researchers want to know if reading about the benefits and risks of oophorectomy (ovary removal) ahead of the surgical consultation improves patients' knowledge and confidence. Adults aged 18 to 65 who were assigned female at birth, identify as transgender or non-binary, and desire a gender-affirming hysterectomy are eligible if they speak English. Participation involves completing surveys before and after your surgical consultation and, for some participants, receiving the educational handout beforehand. This summary was prepared to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHEREducational Handout

educational handout provided to a randomized cohort of patients that reviews the benefits and risks of retaining ovaries vs removing them. This educational handout will be provided prior to the surgical consultation at the time of the initial survey.


Locations(1)

University of Minnesota

Minneapolis, Minnesota, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07324967


Related Trials