Good pain consultation for endometriosis

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled PhD project compares a targeted 'good pain consultation' plus biopsychosocial pain education delivered alongside usual care versus usual care alone for people with endometriosis and related pelvic pain. Participants are randomly assigned to one of the two groups and complete internet-based questionnaires at baseline, 3 months, and 1 year to measure pain self-efficacy and health-related quality of life. The intervention focuses on early integration of pain education and self-management strategies using limited resources within routine clinical practice. The trial is conducted at a single site (Sorlandet Sykehus HF) in Kristiansand, Norway.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* biological women

Exclusion Criteria:

* not speaking norwegian

Where it's running

• Sorlandet Sykehus HF
  Kristiansand, Agder, Norway Recruiting

Study contacts

• Study coordinator: Inger Johanne W Hansen, MD
• Email: inger.johanne.hansen@sshf.no
• Phone: +47 38149424

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• How pelvic organ pain affects muscles and the automatic nervous system in women with painful periods

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• Effects of pelvic organ diseases on endometrial receptivity in infertile women

  This study is trying to see how conditions like adenomyosis, fibroids, and endometriosis affect the ability of the uterus to support pregnancy in women who are having trouble getting pregnant.

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• Measuring L-PGDS levels in blood, urine, vaginal fluid and endometrial tissue

  This project will test whether L-PGDS levels in blood, urine, vaginal fluid and uterine tissue differ between women with adenomyosis, other benign uterine conditions, and healthy controls.

  Recruiting Centre Hospitalier Universitaire de Nīmes · Nîmes · NCT06864494

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.