Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
NCT06212349

Therapeutic-educational Physiotherapy on Pain, Physical-functionality and Quality of Life in Women With Endometriosis.

Led by University of Valencia · Updated on 2025-01-15

62

Participants Needed

1

Research Sites

149 weeks

Total Duration

On this page

Sponsors

U

University of Valencia

Lead Sponsor

H

Hospital Universitario La Fe

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a randomized clinical trial that will be carried out in women with endometriosis divided into two groups: the experimental group (EG) that will receive therapeutic-educational physiotherapy, which will combine therapeutic exercise with a pain education program, and the control group (CG) who will receive the pain education program. The participants will be evaluated at three moments: before starting the study (T1), after the 8-week treatment program (T2) and after another 8 weeks of follow-up in which they will be encouraged to continue with the treatment (T3). The initial assessment will include a medical and physiotherapy history, and at T1, T2 and T3 the following will be assessed: pain, abdominopelvic mobility, muscle status, functionality, sexual function, quality of life, stress and biomarkers of chronic inflammation.

CONDITIONS

Official Title

Therapeutic-educational Physiotherapy on Pain, Physical-functionality and Quality of Life in Women With Endometriosis.

Who Can Participate

Age: 18Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of endometriosis by MRI, ultrasound, or surgery
  • At least 3 months since last surgery if applicable
  • Receiving hormone treatment with disease under control
  • Persistent pelvic pain lasting at least 3 months
  • Presence of pelvic muscle pain, hypertonus, myofascial syndrome, vestibulodynia, or pudendal neuropathy
  • Willingness to participate and provide consent
  • Ability to complete study follow-up visits
  • Access to internet and audiovisual resources for home sessions
Not Eligible

You will not qualify if you...

  • Women in menopausal phase
  • Women undergoing or planning fertility treatment within 3 months
  • Pregnant women
  • Receiving or received physiotherapy treatment in last 3 months
  • Recent lower limb fracture in last 3 months limiting function
  • Cognitive illness interfering with understanding exercises
  • Acute musculoskeletal pathology or neuropathy
  • History or current neoplastic disease
  • Untreated endometriosis
  • Acquired genital or pelvic floor abnormalities
  • In litigation, compensation claims, or pending disability status
  • Severe mental illness such as schizophrenia or borderline personality disorder

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospital Universitari i Politècnic La Fe,

Valencia, Spain, 46026

Actively Recruiting

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Research Team

I

Irene Juarez, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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