Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID06822582

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

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

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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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