Effect of Tele-Yoga on Pain, Fatigue, and Quality of Life in Endometriosis (NCT07241637) | Clinical Trial Compass
CompletedNot Applicable
Effect of Tele-Yoga on Pain, Fatigue, and Quality of Life in Endometriosis
Turkey (Türkiye)60 participantsStarted 2025-09-01
Plain-language summary
This study aims to examine the effects of Tele-yoga on chronic pelvic pain, fatigue, and quality of life in patients diagnosed with endometriosis. It will be conducted as a single-center, randomized controlled experimental study design.
Who can participate
Age range
18 Years – 65 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria
* Voluntary willingness to participate in the study.
* Ability to communicate effectively, with no language barriers.
* Completion of at least primary school education.
* Aged 18 years or older.
* Premenopausal.
* Mild (1-3) or moderate (4-6) chronic pelvic pain.
* Not pregnant.
* No use of any complementary and integrative health practice during the study period.
* No regular exercise (defined as exercising more than three times per week).
* No physiotherapy within the previous 3 months.
* No pelvic surgery within the previous year.
* No planned surgical treatment for endometriosis.
* No other injury or medical condition causing pelvic pain.
* Access to a computer, smartphone, or tablet with a camera and a stable internet connection to participate in the online sessions.
Exclusion Criteria
* Participant's request to withdraw from the study at any stage.
* Failure to attend all tele-yoga sessions.
* Initiation of regular exercise or physiotherapy during the study period.
* Pregnancy during the study period.
* Decision to undergo surgical treatment during the study period.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Numerical Rating Scale (NRS)
Timeframe: The scale was administered to all groups before the intervention began and after the intervention was completed (at the end of the eighth week).