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Pre-Rehabilitation for Female Patients Undergoing Pelvic Radiotherapy

NCT06059586

This study is recruiting at 3 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to examine the feasibility of adding pre-rehabilitation pelvic health physical therapy to standard of care radiation therapy treatment plan for female patients who have been diagnosed with cervical, vaginal, vulvar, uterine, or anal cancer and are a candidate for curative pelvic radiation with external beam. Participants will receive education on using a vaginal dilator for use during treatment and complete questionnaires looking at pain and sexual function.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Dyspareunia
  • Pelvic Pain
  • Sexual Dysfunction
  • Radiation Toxicity

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
18 years and older
Sex
Female
Healthy volunteers
Not accepted
Sponsor
Indiana University
Last updated on ClinicalTrials.gov
September 18, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Indiana · 3

  • IU Health West · Avon, IN
  • IU Health Schwarz Cancer Center · Carmel, IN
  • Indiana University Melvin and Bren Simon Comprehensive Cancer Center · Indianapolis, IN

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.