Improving Access to Pelvic Health Physiotherapy for Endometriosis
RecruitingNCT07731776
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Brief summary (from the registry)
This is a mixed-methods study aimed to generate new evidence to help optimize access to pelvic health physiotherapy (PHPT) for women living with endometriosis in the province of Quebec (Canada). Specifically, the objectives are to: Obj. 1: Understand the patient journey of women living with endometriosis, including their experiences accessing PHPT. Obj. 2: Describe current PHPT clinical practices and service delivery for women living with endometriosis in Quebec. Obj. 3: Identify barriers, facilitators and potential strategies to improve access to PHPT services and optimize the patient journey of women living with endometriosis in Quebec. Findings will inform clinical, organizational and policy recommendations to strengthen the integration of PHPT within multidisciplinary endometriosis care. The project is divided into three sequential parts: Part 1: Semi-structured individual interviews (open-ended questions) will be conducted with women living with endometriosis to explore their journey to obtain endometriosis care, experiences accessing PHPT and perceived barriers and facilitators. Approximately 15-20 participants will be recruited until data saturation is reached. Part 2: An online cross-sectional survey will be conducted among pelvic health physiotherapists practicing in the province of Quebec, Canada to describe current clinical practices, service delivery and challenges related to the management of women living with endometriosis. The minimum expected sample size is 225 physiotherapists . Part 3: Semi-structured focus groups (open-ended questions) will be conducted with women living with endometriosis, pelvic health physiotherapists, physicians and healthcare managers to identify and prioritize strategies to improve access to PHPT services. Approximately 24-32 participants will be recruited across four focus groups. Across all three parts, recruitment strategies will aim to ensure diversity in participant characteristics, including geographic region, sociodem…
Study details
- Official title
- Optimizing Care and Improving Access to Pelvic Health Physiotherapy for Women Living With Endometriosis: A Portrait of the Current Situation and Recommendations for Possible Solutions in Quebec (Canada)
- Conditions
- Sponsor
- Université de Sherbrooke
- Collaborators
- Réseau Québécois de Recherche sur la Douleur (RQRD); Association Québécoise de la Physiothérapie (AQP)
- Start date
- 2026-07-28
- Primary completion
- 2027-03-29
- Sex
- Female
- Age range
- from 18 Years to 45 Years
- Results posted
- No results posted in this snapshot
- Countries
- Canada
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria (part 1): * Female (biological sex at birth) * Aged between 18 and 45 years old * Residing in the province of Quebec, Canada * Able to speak and understand French * Has a confirmed or suspected diagnosis of endometriosis Inclusion Criteria (part 2): * Licensed physiotherapist authorized to practice pelvic health physiotherapy in Quebec, Canada * Currently practicing in the province of Quebec, Canada * Provides pelvic health physiotherapy services to women experiencing symptoms associated with endometriosis Inclusion Criteria (part 3): Women living with endometriosis: * Female (biological sex at birth) * Aged between 18 and 45 years old * Residing in the province of Quebec, Canada * Able to speak and understand French * Has a confirmed or suspected diagnosis of endometriosis Healthcare providers/managers: \- Has experience providing, coordinating, organizing or managing care for women with confirmed or suspected endometriosis in the province of Quebec, Canada
Canadian sites (1)
| Facility | City | Province |
|---|---|---|
| Centre hospitalier universitaire de Sherbrooke | Sherbrooke | Quebec |
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07731776