NCT06517654Completed
Comparison of the Effectiveness of EMG-Biofeedback and Rebound Therapy in Patients With Endometriosis
Source: ClinicalTrials.gov · Last updated 21 Apr 2026
Brief summary (registry, in English)
The aim of our study is to investigate the effects of pelvic floor muscle strengthening exercises with EMG-Biofeedback and pelvic floor muscle strengthening exercises with Rebound therapy on pelvic floor muscle strength, pain level, NGF level, perceived stress level, quality of life and sleep in women diagnosed with endometriosis.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 42 (actual)
- First submitted
- 11 Jul 2024
- Start date
- 1 Sept 2024
- Primary completion date
- 1 Nov 2025
- Lead sponsor
- Medipol University
- Diseases
- Endometriosis
- NCT number
- NCT06517654
What you commit to
- Study type: Interventional
- Participants enrolled: 42
- From 1 Sept 2024 to the primary completion date, 1 Nov 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Being receiving medical treatment for endometriosis,
Other illness
- Presence of gynecological bleeding,
- Active vaginal or urinary tract infection,
- Presence of a neurological or orthopedic disease affecting the lower extremity,
- History of spine and/or lower extremity orthopedic surgery,
- Presence of uncontrolled hypertension and cardiovascular disease.
Other
- Being included in another study during the study period,
- Presence of communication and cooperation problems,
- Presence of tubo-ovarian abscess,
- Pregnancy and giving birth within the last 12 months,
- Presence of impaired somatosensory status,
- Not attending 2 consecutive sessions.
- In addition to the exclusion criteria determined for the EMG-Biofeedback Group;
- Presence of severe arthritis affecting the spine and/or lower extremity,
Who the study is looking for
- Being between 20-50 years old,
- Being diagnosed with endometriosis,
- Completing the voluntary consent form,
- Pain level being at least 4 on the Visual Analog Scale (VAS).
Age in the registry: 20 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Zeynep Kamil Women and Children's Diseases Training and Research Hospital Coordinator of this site? Confirm its status | Üsküdar | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.