Massage and hydrotherapy for improving well-being and pain in endometriosis patients
Effect of Massage and Hydrotherapy to Improve Well-being and Pain Perception in Women With Endometriosis Unresponsive to Conventional Treatment
This study is testing whether a special relaxation treatment that includes massage and hydrotherapy can help women with endometriosis feel better and reduce their pain.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 18 Years to 55 Years |
| Sex | Female |
| Sponsor | Universidad de Granada Academic / other |
| Locations | 1 site (Granada) |
| Trial ID | NCT06506708 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the short-term effects of a comprehensive HAMMAM experience, which includes therapeutic hydrotherapy, aromatherapy, music therapy, and Swedish massage, on women suffering from endometriosis-related chronic pelvic pain. A total of 44 women will be randomly assigned to either an intervention group, receiving the HAMMAM experience alongside their usual gynecological treatment, or a control group, receiving only standard care. The intervention consists of three sessions over six weeks, focusing on relaxation and pain reduction. Participants will be assessed before and after the intervention to measure changes in well-being and pain perception.
Who should consider this trial
Good fit: Ideal candidates are premenopausal women diagnosed with endometriosis who experience chronic pelvic pain.
Not a fit: Patients with acute or terminal illnesses, recent fractures, or other chronic conditions that interfere with participation may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the quality of life and pain management for women with endometriosis.
How similar studies have performed: While similar approaches have been explored, this specific combination of therapies in a HAMMAM setting is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pelvic pain during the last 6 months more or equal to 4 in a NRS scale. * Diagnosed with endometriosis (through surgery, magnetic resonance imaging or ultrasound imaging) * Premenopausal status * Be able to walk without assistance and to read and write enough * Be capable and willing to provide consent Exclusion Criteria: * Acute or terminal illness * A recent fracture in any upper or lower extremity (\<3 months), disc herniation and any chronic disease or orthopaedic issues that would interfere with her ability to participate in this intervention program * Express unwillingness to complete the study requirements * Be involved in other rehabilitation program
Where this trial is running
Granada
- Francisco Artacho Cordón — Granada, Spain (Recruiting)
Study contacts
- Principal investigator: Francisco Artacho-Cordón — Universidad de Granada
- Study coordinator: Francisco Artacho-Cordón
- Email: fartacho@ugr.es
- Phone: 958249983
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.