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NCT06059586 · ClinicalTrials.gov registry record · NA

Pre-Rehabilitation for Female Patients Undergoing Pelvic Radiotherapy

A NA study of Pelvic Pain and Sexual Dysfunction, sponsored by Indiana University.

Recruiting
Registry status
NA
Development phase
20
Enrollment target
3
Study locations

NCT06059586 is a NA study of Pelvic Pain and Sexual Dysfunction that is actively recruiting participants, run by Indiana University. The registered enrollment target is 20 participants, below the 371-participant average among 23 other Pelvic Pain trials with a reported enrollment target (95% lower). The trial reports 3 study locations across 1 state.

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The verdict

NCT06059586, a NA study of Pelvic Pain and Sexual Dysfunction, is actively recruiting participants, sponsored by Indiana University.

RECRUITING
Registry status
NA
Development phase
20 participants
Enrollment target
3
Study locations

Study 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.

Interventions

  • BEHAVIORAL Pelvic health therapy
  • DEVICE Dilator feasability

Study Locations (3)

Indiana

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

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-01-16
Est. Completion 2027-06
Phase NA

Sponsor

Indiana University

890 total trials

What the Registry Record Tells You About NCT06059586

The ClinicalTrials.gov registry entry for NCT06059586 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 371-participant average among 23 other Pelvic Pain trials with a reported enrollment target (95% lower). The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Pelvic Pain appearing as the primary indexed condition, and to 2 interventions - of which Pelvic health therapy is the first listed.

NCT06059586 reports 3 study locations spanning 1 distinct geographic area - top geographies include Indiana.

Frequently Asked Questions

What is clinical trial NCT06059586 about?

NCT06059586 is a clinical study titled "Pre-Rehabilitation for Female Patients Undergoing Pelvic Radiotherapy". 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 curativ...

What is the current status of trial NCT06059586?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-01-16. Estimated completion is 2027-06.

What conditions does trial NCT06059586 study?

This clinical trial studies the following conditions: Pelvic Pain, Sexual Dysfunction, Radiation Toxicity, Dyspareunia.

What interventions are being tested in trial NCT06059586?

The interventions under investigation include: Pelvic health therapy (BEHAVIORAL), Dilator feasability (DEVICE).

Who is sponsoring clinical trial NCT06059586?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06059586 being conducted?

This trial has 3 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.