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Influence of Bodily Practices on the Quality of Life of Women With Endometriosis

Influence of Bodily Practices on the Quality of Life of Women

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06660043
Acronym
PCKendo
Enrollment
52
Registered
2024-10-26
Start date
2024-03-21
Completion date
2026-07-01
Last updated
2026-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

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.

Interventions

OTHERphysical activity

40 min circuit training session

OTHERanalgesic physical therapy

physical therapy with massage and Transcutaneous Electrical Nerve Stimulation in a 40min session

OTHERanalgesic physical therapy AND physical activity

25 min circuit training session and 15 min physical therapy

Sponsors

Fondation Hôpital Saint-Joseph
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
No

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;

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of quality of life6monthsEndometriosis Health Profile-30 (EHP-30) questionnaire

Secondary

MeasureTime frameDescription
Global Self Esteem evaluationat enrollement, 3 and 6 months after enrollementRosenberg questionnaire
evaluation of physical self esteemat enrollement, at 3 and 6 months after enrollementPhysical Self Description questionnaire - short form (PSDQ-S)
Pain Evaluationat enrollement, 3 and 6 months after enrollementNumerical pain rating scale

Countries

France

Contacts

PRINCIPAL_INVESTIGATORFrederique PERROTTE

Fondation Hôpital Saint-Joseph

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026