NCT06660043 Influence of Bodily Practices on the Quality of Life of Women With Endometriosis
| NCT ID | NCT06660043 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Fondation Hôpital Saint-Joseph |
| Condition | Endometriosis |
| Study Type | INTERVENTIONAL |
| Enrollment | 90 participants |
| Start Date | 2024-03-21 |
| Primary Completion | 2025-03-20 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 90 participants in total. It began in 2024-03-21 with a primary completion date of 2025-03-20.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This research focuses on understanding how physical activity can improve the quality of life for women with endometriosis by enhancing their self-perception, particularly regarding their physical abilities and appearance. The study is based on the idea that improving internal perceptions can lead to better overall well-being for these women. Previous studies, suggest that physical self-perception plays a crucial role in shaping an individual's quality of life. There is also evidence supporting a reciprocal relationship between physical self-concept and participation in physical activity In this context, the research aims to explore how physical activity could positively influence the self-concept of women suffering from endometriosis, which in turn could enhance their quality of life. By focusing on improving both physical abilities and body image through regular exercise, this study seeks to offer insights into potential therapeutic approaches for managing the physical and psychological impacts of endometriosis.
Eligibility Criteria
Inclusion Criteria: * Menstruating women aged 18 to 55; * proven diagnosis of endometriosis (pelvic ultrasound or MRI) * Having endometriosis-related pain of a level higher than 3 on the VAS scale and/or chronic incapacitating symptoms related to endometriosis; * Patient without treatment or with stable endometriosis treatment (pill and/or ATG) who has not undergone treatment during the last 6 months; * Patient affiliated to a health insurance scheme; * French-speaking patient; * Patient having given free, informed and express oral consent. Exclusion Criteria: * Any patient whose endometriosis treatment has been modified for less than 6 months; * Having endometriosis-related pain greater than or equal to 8 on the VAS scale; * Cardiovascular risks related to physical training; * Inability to perform proposed exercises; * Patient under guardianship; * Patient deprived of liberty;
Contact & Investigator
Frederique PERROTTE
PRINCIPAL INVESTIGATOR
Fondation Hôpital Saint-Joseph
Frequently Asked Questions
Who can join the NCT06660043 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 55 Years, studying Endometriosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06660043 currently recruiting?
Yes, NCT06660043 is actively recruiting participants. Contact the research team at fperrotte@ghpsj.fr for enrollment information.
Where is the NCT06660043 trial being conducted?
This trial is being conducted at Chevry-Cossigny, France, Paris, France.
Who is sponsoring the NCT06660043 clinical trial?
NCT06660043 is sponsored by Fondation Hôpital Saint-Joseph. The principal investigator is Frederique PERROTTE at Fondation Hôpital Saint-Joseph. The trial plans to enroll 90 participants.