Clinical trial Recruiting at 2 sites Interventional Ages 18 and up Women only

Online pelvic health program for breast and gynecologic cancer survivors

Official title: A Pelvic Health eModule to Address Urogenital Impairments After Breast and Gynecologic Cancer: a Pilot Prospective Interventional Study

Run by Laval University · NCT06822582 · Data updated 2026-11-12

This study is testing an online program to help breast and gynecologic cancer survivors improve their pelvic health and quality of life through group sessions with a physiotherapist.

More Breast Cancer Female trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment20 (estimated)
SponsorLaval University
Academic / other
Drugs / interventionschemotherapy, radiation
Locations2 sites (Edmonton, Alberta and 1 other locations)
StatusRecruiting
StartedJanuary 7, 2025
Main results expectedDecember 2025
Study endsJune 2026
Registry record updatedFebruary 12, 2025
Trial IDNCT06822582 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 18 who have been diagnosed with breast or gynecologic cancer and are experiencing pelvic health dysfunction.

Probably not a fit

Patients without regular access to the internet or smart devices may not benefit from this online program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The GYVE study tests an online program designed for individuals who have had breast or gynecologic cancer and are facing pelvic health issues such as urinary incontinence and sexual pain. This 12-week program includes weekly online group sessions led by a physiotherapist, focusing on pelvic floor muscle training, hydration, diet, and pain management. The study aims to evaluate the feasibility and acceptability of the program while exploring its preliminary effectiveness in reducing urogenital impairments. Participants will be recruited from Quebec and Edmonton, with the goal of providing valuable insights into the program's impact on quality of life for cancer survivors.

Why it matters

Potential benefit: If successful, this program could significantly improve pelvic health and quality of life for cancer survivors experiencing related issues.

How similar studies have gone: While similar approaches have been explored, this specific online intervention for pelvic health in cancer survivors is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* be \>18 years of age;
* have received a diagnosis of breast or gynecological (endometrial, cervical, ovarian, vulvar or vaginal) cancer (Stage I-IV) ;
* be on active cancer treatment or have completed any cancer treatment (surgery and/or radiation therapy and/or chemotherapy) within the last 3 years;
* be able to provide informed written consent in English or French;
* have a urogenital dysfunction, as screened by a score of ≥ 2 on the Pelvic Floor Bother Questionnaire.

Exclusion Criteria:

* do not have regular access to internet, to a smart device or a computer, at home.

Where it's running

  • University of Alberta
    Edmonton, Alberta, Canada
    Recruiting
  • Centre interdisciplinaire de recherche en réadaptation et intégration sociale
    Québec, Quebec, Canada
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.