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NCT07134023Recruiting

Educational Program for the Multidisciplinary Support of Patients With Endometriosis

Programme EducaTif d'Accompagnement pLuridisciplinaire Des Patientes Atteintes d'Endométriose

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

Background: Endometriosis is a chronic gynecological condition characterized by the ectopic presence of endometrial tissue outside the uterine cavity. It affects approximately 2 to 10% of women of reproductive age and up to 50% of women with chronic pelvic pain. In France, between 1.5 and 2.5 million women are estimated to be affected. Endometriosis significantly impairs quality of life, with consequences on cognitive, behavioral, sexual, and emotional well-being, and has substantial socio-economic impact. Rationale: Current medical and surgical treatments primarily aim to reduce pain and preserve fertility but show limited effectiveness and are often discontinued due to adverse effects. Many women resort to self-management strategies, which may pose risks if not properly supervised. A multidisciplinary and integrative approach is essential to address the complex and multifactorial symptoms of endometriosis. Therapeutic patient education (TPE) is a recommended strategy that can empower patients in the management of chronic conditions, yet remains underdeveloped in endometriosis care pathways. Objective: This study aims to evaluate the effectiveness of a multidisciplinary educational program combined with nurse-led telephone follow-up on the quality of life of patients with endometriosis. Methods: The intervention will consist of a series of workshops led by various healthcare professionals (medical and paramedical), alongside regular nurse-led telephone follow-up. This approach intends to provide continuous support, assess patients' evolving needs, and facilitate access to supportive care services, particularly within regional endometriosis networks (ENDAURA and ENDOSUD). Expected Outcomes: The study will assess whether this intervention improves quality of life among women with endometriosis. It also aims to provide evidence for the scalability and transferability of such a program at a national level, in alignment with current public health priorities.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
260 (estimated)
First submitted
7 Aug 2025
Start date
17 Dec 2025
Primary completion date
1 Jan 2029
Lead sponsor
Centre Hospitalier Emile Roux
NCT number
NCT07134023

What you commit to

  • Study type: Interventional
  • Planned participants: 260
  • From 17 Dec 2025 to the primary completion date, 1 Jan 2029
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient having already participated in an educational program or received multidisciplinary follow-up (involving at least 3 different healthcare professionals simultaneously within the same facility) in the past 12 months,

Other

  • Patient in an emergency situation, or under legal protection measures (guardianship, curatorship, or judicial protection) and unable to give consent,
  • For patients at the experimental center only: inability to comply with study follow-up due to geographical, social, or psychological reasons.

Who the study is looking for

  • Signed informed consent,
  • Age ≥ 18 years,
  • Patient diagnosed with endometriosis confirmed by pelvic ultrasound and/or MRI,
  • Patient experiencing chronic pelvic-perineal pain (± dysmenorrhea, dyspareunia, etc.) for at least 3 months,
  • Ability to read and understand French,
  • Affiliation with a social security system or equivalent.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinique Axium
Coordinator of this site? Confirm its status
Aix-en-ProvenceFranceRecruiting
Centre Hospitalier Emile Roux
Coordinator of this site? Confirm its status
Le Puy-en-VelayFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.