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Clinical Trials in Canada / NCT06822582
Recruiting Not applicable

Pelvic Health Rehabilitation After Breast and Gynecologic Cancer

NCT06822582 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-01-07
Last updated
2025-02-12

Condition(s) studied

Gynecologic CancersBreast Cancer FemaleIncontinenceIncontinence BowelSexual DysfunctionVaginal Atrophy, Sexual Dysfunction, Vaginal Dryness, DyspareuniaConstipation

Investigational drug(s) / intervention(s)

Pelvic Health Module

Pelvic Health Module: Telerehabilitation program involving pelvic floor exercises, education and counselling.

Study summary

The GYVE study aims at testing an online program (eModule) to help people who have had breast or gynecologic cancer and are experiencing pelvic health issues like urinary incontinence and pain during sex. These cancers and their treatments can cause significant pelvic health problems, affecting daily life and quality of life. Physiotherapy can help, but access is often limited due to costs and other barriers. The study will involve 20 participants from Quebec and Edmonton, who will take part in a 12-week program with weekly online group sessions led by a physiotherapist. Topics include pelvic floor muscle training, use of vaginal moisturizers, hydration, diet, and pain management. Led by experts in cancer rehabilitation and pelvic health, the study aims to provide valuable information on the feasibility and effectiveness of the eModule, potentially leading to broader implementation to help more people with lived experience of cancer.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (2)

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

More Laval University trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06822582 on ClinicalTrials.gov ↗ ← All trials in Canada