Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
Healthy Volunteers
ID07241637

The Effect of Tele-Yoga Application on Chronic Pelvic Pain, Fatigue and Quality Of Life In Women With Endometriosis Diagnosis

Led by Ankara University · Updated on 2025-11-25

66

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to examine how Tele-yoga affects chronic pelvic pain, fatigue, and quality of life in women diagnosed with endometriosis. Endometriosis is a chronic condition affecting many women of reproductive age, causing symptoms like pain and fatigue that can significantly impact daily life. The study uses a randomized controlled experimental design to explore how a mind-body approach like yoga, delivered remotely, can support women with this condition. Participants will be divided into two groups. The intervention group will take part in 16 live Tele-yoga sessions over eight weeks, with two 60-minute sessions each week conducted via Google Meet. Each session includes breathing exercises, meditation, warm-up stretches, a yoga flow combining postures and breathing techniques, and deep relaxation. The control group will not receive any intervention but will be followed for the same period and complete assessments. During the study, participants will complete several scales before and after the eight-week period, including the Numerical Rating Scale for pain, the Fatigue Severity Scale, and the Endometriosis Health Profile-5 for quality of life. The study also monitors adherence to the yoga sessions and collects data on pain, fatigue, and life quality to evaluate the effects of the Tele-yoga program. The total participation duration is eight weeks.

CONDITIONS

Brief Title

Effect of Tele-Yoga on Pain, Fatigue, and Quality of Life in Endometriosis

Who Can Participate

Age: 18Years - 65Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Voluntarily agree to participate in the research
  • Able to communicate effectively and have no language barriers
  • Have at least a primary school education
  • Are 18 years of age or older and premenopausal
  • Are not pregnant
  • Have no health problems that would prevent them from practicing yoga
  • Do not exercise regularly or exercise no more than three times per week
  • Have not received physical therapy within the past three months
  • Have not undergone any pelvic surgery within the past year
  • Do not have surgical treatment planned for endometriosis
  • Do not have any other injury or disease causing pelvic pain
  • Have mild (1-3) or moderate (4-6) chronic pelvic pain
  • Have access to a computer, phone, or tablet with a camera and an available internet connection to participate in online sessions
Not Eligible

You will not qualify if you...

  • Wish to withdraw at any stage of the research
  • Do not attend all Tele-yoga sessions
  • Begin regular exercise or physical therapy during the study period
  • Become pregnant during the study
  • Use any Complementary or Alternative Medicine (CAM) method during the intervention
  • Undergo surgical treatment during the course of the study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Outpatient Treatment

Duration - 8 weeks

Participants in the Tele-Yoga group attend online yoga sessions twice a week for eight weeks, each lasting 60 minutes, conducted live via an electronic platform.

16 online sessions over 8 weeks

Outpatient Treatment

Duration - 8 weeks

Participants in the Control group are observed without intervention and complete evaluations at the end of the eight-week period.

1 evaluation visit at the end of 8 weeks

Trial Site Locations

Total: 1 location

1

Ankara University Nursing Faculty

Ankara, Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

M

Melek Ha Köprülü

F

Funda Özdemir, Prof. Dr.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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