Actively Recruiting
A Pelvic Health eModule to Address Urogenital Impairments After Breast and Gynecologic Cancer: a Pilot Prospective Interventional Study
Led by Laval University · Updated on 2025-02-12
20
Participants Needed
2
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new online program called the Pelvic Health eModule to support women who have had breast or gynecologic cancer and are experiencing pelvic health issues such as urinary incontinence and pain during sex. These cancers and their treatments can cause significant pelvic problems that affect daily life and quality of life. The study aims to test how practical and acceptable the eModule is, as well as to explore its early effectiveness in reducing pelvic health impairments. The study involves 20 female participants from Quebec and Edmonton who have had breast or gynecologic cancer and currently have pelvic health dysfunction. Participants will join a 12-week program featuring weekly live online group sessions led by a registered physiotherapist specialized in pelvic health. The sessions cover pelvic floor muscle training, use of vaginal moisturizers, hydration, diet, and pain management. The program is delivered in French or English and focuses on telerehabilitation combining exercises, education, and counseling. During the study, participants will complete questionnaires before, during, and after the intervention to assess how well the program works and how satisfied they are. Researchers will monitor attendance, completion rates, and changes in pelvic health symptoms using the Pelvic Floor Bother Questionnaire. The study will protect participants' privacy and obtain informed consent. It runs over several months including preparation, recruitment, intervention, and analysis phases, aiming to inform future broader use of this online pelvic health program for cancer survivors.
CONDITIONS
Brief Title
Pelvic Health Rehabilitation After Breast and Gynecologic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be 18 years of age or older
- Have a diagnosis of breast or gynecologic cancer (endometrial, cervical, ovarian, vulvar, or vaginal cancer) at any stage (I-IV)
- Be currently on active cancer treatment or have completed treatment (surgery, radiation, or chemotherapy) within the last 3 years
- Be able to provide informed written consent in English or French
- Have pelvic health dysfunction, shown by a score of 2 or higher on the Pelvic Floor Bother Questionnaire
You will not qualify if you...
- Do not have regular access to the internet, a smart device, or a computer at home
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 12 weeks
Participants take part in a 12-week online pelvic health rehabilitation program including weekly live group exercises and educational sessions led by a physiotherapist.
Weekly online group sessions
Trial Site Locations
Total: 2 locations
1
University of Alberta
Edmonton, Alberta, Canada, T6G2G4
Actively Recruiting
2
Centre interdisciplinaire de recherche en réadaptation et intégration sociale
Québec, Quebec, Canada, G1M2S8
Actively Recruiting
Research Team
S
Stéphanie Bernard, Ph.D. PT
C
Clémence Bélanger, M.Sc. PT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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