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Pelvic Floor Physical Therapy and Exercise for Women With Endometriosis and Chronic Pelvic Pain

Pelvic Floor Physical Therapy and Exercise for Women With Endometriosis and Chronic Pelvic Pain

Recruiting
18-45 years
Female
Phase N/A

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Overview

Endometriosis is a chronic gynecological condition that can cause persistent pelvic pain, painful menstruation, painful sexual intercourse, and reduced quality of life. This study will evaluate whether specialized pelvic floor physical therapy combined with a structured physical exercise program is more effective than a placebo intervention combined with the same exercise program in reducing chronic pelvic pain in women with endometriosis. Participants will be randomly assigned to one of the two groups and followed for 12 weeks.

Description

Endometriosis is a chronic estrogen-dependent inflammatory disease frequently associated with chronic pelvic pain, dysmenorrhea, dyspareunia, impaired quality of life, sexual dysfunction, and central pain sensitization. Although pelvic floor physical therapy and exercise have demonstrated potential benefits, high-quality randomized placebo-controlled trials evaluating their combined effects remain limited.

This study is a prospective, double-blind, randomized, placebo-controlled clinical trial designed to evaluate the effectiveness of specialized pelvic floor physical therapy combined with a structured physical exercise program compared with a placebo intervention combined with the same exercise program in women with confirmed endometriosis and chronic pelvic pain.

Sixty-four participants will be randomly allocated (1:1) to either the intervention group or the placebo group. Both groups will participate in the same 12-week progressive exercise program. The intervention group will receive specialized pelvic floor physical therapy, whereas the control group will receive a placebo pelvic floor physical therapy protocol designed to maintain participant blinding without providing specific therapeutic effects.

Participants will be evaluated at baseline (week 0), after 8 weeks, and at the end of the 12-week intervention. The primary outcome is the intensity of chronic pelvic pain. Secondary outcomes include neuropathic pain symptoms, central sensitization, quality of life, sexual function, depressive symptoms, pelvic floor muscle function, treatment adherence, and participant satisfaction.

Eligibility

Inclusion Criteria:

  • Female, aged 18 to 45 years.
  • Diagnosis of endometriosis confirmed by surgery and/or imaging examinations.
  • Chronic pelvic pain for at least 6 months.
  • Visual Analog Scale (VAS) score ≥4 for chronic pelvic pain.
  • Willingness and ability to provide written informed consent and comply with all study procedures.

Exclusion Criteria:

  • Current pregnancy or planned pregnancy during the study period.
  • Pelvic surgery within the previous 3 months.
  • Neuromodulation treatment within the previous 3 months.
  • Medical or musculoskeletal conditions that contraindicate participation in pelvic floor physical therapy or the exercise program.

Study details
    Endometriosis
    Chronic Pelvic Pain

NCT07733583

Hospital de Clinicas de Porto Alegre

1 August 2026

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