Effect of Tele-Yoga on Pain, Fatigue, and Quality of Life in Endometriosis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorAnkara University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
Those who wish to withdraw at any stage of the research
Those who do not attend all Tele-yoga sessions
Those who begin regular exercise or physical therapy during the study period
Those who become pregnant during the study
Trial design
Design model
Parallel
Treatments tested in this trial
Tele-Yoga Group
BehavioralTele-yoga is a telerehabilitation method that enables the delivery of yoga-based rehabilitation services through electronic systems. Initially developed for emergency management, this approach has become effective in daily practice with the increasing cost of treatment and the privatization of healthcare services. Yoga is a practice that can be adapted to the individual needs of each woman. In women with endometriosis, yoga helps develop a different response to pain through mindful attention to painful areas, relaxation postures, breathing techniques, and movement sequences
Treatment groups
66 Participants
are divided into 2 treatment groupsGroup A: Tele-Yoga GroupExperimental treatment 1 intervention
Group B: Control GroupNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Numerical Rating Scale (NRS)
In patients diagnosed with endometriosis, the Numerical Rating Scale (NRS) is used to assess pain intensity by having the patient rate their perceived pain on a scale from 0 to 10.A value of 0 is considered "no pain," while a value of 10 is considered "the worst pain imaginable." Patients are asked to circle the number representing the amount of pain they experience during the assessment. As the number on the scale increases, the pain increases.
Time frame
The scale will be administered to all groups before the intervention begins and after the intervention is completed (at the end of the eighth week)Secondary outcomes
1
The Fatigue Severity Scale (FSS)
The Fatigue Severity Scale (FSS) is used to determine how fatigued the patient has felt over the past week, including the day the test is administered.
Time frame
The scale will be administered to all groups before the intervention begins and after the intervention is completed (at the end of the eighth week).2
The Endometriosis Health Profile-5 (EHP-5)
The Endometriosis Health Profile-5 (EHP-5) is used to assess the impact of endometriosis on women's quality of life.
Time frame
The scale will be administered to all groups before the intervention begins and after the intervention is completed (at the end of the eighth week)Sponsors and contacts
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Source ClinicalTrials.gov