Ireland
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Starting soon Not applicable

Perioperative Yoga Therapy and Endometriosis Surgery

NCT07765680 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-10-01
Last updated
2026-10-02

Condition(s) studied

EndometriosisChronic PainImpairment of Quality of Life

Investigational drug(s) / intervention(s)

Standard surgical management for endometriosisStructured perioperative yogatherapy programme plus standard surgical management

Standard surgical management for endometriosis: Participants undergo the indicated surgery for endometriosis and receive standard perioperative and follow-up care, without study yoga therapy sessions. They complete the same scheduled clinical and patient-reported assessments as the intervention group.

Structured perioperative yogatherapy programme plus standard surgical management: Participants undergo the indicated surgery for endometriosis and receive 32 live, guided yoga therapy sessions: 16 sessions during the 2 months before surgery and 16 sessions during the 3 months after surgery. Sessions are delivered by healthcare professionals trained in yoga therapy and combine adapted postures, breathing techniques, and meditative practices. A secure digital platform provides videos, audio materials, questionnaires, support for independent practice, and pseudonymised monitoring of session opening, initiation, interruption, completion, validation, frequency, and regularity.

Study summary

YOGENDOCHIR is a multicentre, prospective, randomised, controlled, parallel-group study involving 188 adult women scheduled to undergo surgery for endometriosis.

The study compares standard surgical management alone with the same management combined with a structured perioperative yoga therapy programme comprising 32 guided sessions (16 before and 16 after surgery), supplemented by a secure digital platform supporting independent practice and adherence monitoring.

The primary objective is to assess the effect of yoga therapy on endometriosis-related pain, as measured by the pain subscale of the Endometriosis Health Profile-30 (EHP-30). Participants are assessed before surgery and at 3, 6, and 12 months after the procedure.

Secondary outcomes include quality of life, pain characteristics, fatigue, sleep, anxiety and depressive symptoms, sexual health, kinesiophobia, activities of daily living, medication use, healthcare utilisation, absenteeism, adherence, satisfaction, and the participants' ability to use the platform independently.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
* Adult woman (18 years or older) covered by a social health insurance scheme. * Surgery for endometriosis is indicated. * No assisted reproductive technology (ART) protocol planned within 6 months after surgery. * No chronic pain attributable to another disease or condition. * No yoga practice outside the study during participation.

Primary outcome measure(s)

  • Change in endometriosis-related pain measured by the EHP-30 pain subscale — baseline3 Months6 monthes12 months after surgery
    Between-group difference in change from the preoperative baseline in the pain subscale of the Endometriosis Health Profile-30 (EHP-30), comparing perioperative yoga therapy plus standard surgery with standard surgery alone. The sample-size calculation is based on detecting an additional clinically relevant 11-point reduction in the EHP-30 pain subscore.

Trial sites (4)

FacilityCityRegionStatus
CHU Amiens Amiens France
CH de Calais Calais France
CHU de Lille Lille France
CHU de Lille Lille France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07765680 on ClinicalTrials.gov ↗ ← All trials in France