Clinical Trials in Norway / NCT07205614
Recruiting Not applicable

The Good Pain Consultation in Endometriosis.

NCT07205614 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2025-11-01
Last updated
2026-04-28

Condition(s) studied

Pelvic Pain SyndromeEndometriosisDysmenorrheaAdenomyosisPeriod PainMenstrual Pain

Investigational drug(s) / intervention(s)

pain consultation, biopsychosocial pain education + usual careUsual Care

pain consultation, biopsychosocial pain education + usual care: Participants will receive a link to a digital pain education program. The program will include standard information about endometriosis, but will also introduce a biopsychosocial understanding of pain including influence of psychological factors such as excessive worry, stress, sleep disturbance and emotional distress. Self-management strategies including physical activity, relaxation and breathing techniques, cognitive techniques, psychosocial support and appropriate use of pain medication and supplemental treatment (e.g. physical therapy, TENS, heat), will be introduced. Participants will then attend a single "good pain consultation", a patient-centered consultation with a clinician associated with the project, in which content from the educational package will be reinforced. The consultation will provide the opportunity to address the biopsychosocial factors including anxiety, previous trauma, emotional distress etc. Shared decision-making regarding preferred self-management strat

Usual Care: Usual follow up at the department of gynecology

Study summary

This PhD project investigates the effect of "the good pain consultation" and early integration of biopsychosocial pain education with current standard management of endometriosis. Our goal is to facilitate self-management of pain and improve health-related quality of life (HRQOL) using limited resources.

Our research question is: Does a good pain consultation improve pain self-efficacy and HRQOL, compared to usual care at 3 months and 1 year.?

Researchers will compare a good pain consultation to a control group that will receive usual care.

Participants will:

Attend a consultation and biopsychososial pain education plus usual care or usual care alone.

They will answer questions in an internet-based questionnaires three times point during the study.

Eligibility

Sex
FEMALE
Min age
16 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * biological women Exclusion Criteria: * not speaking norwegian

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sorlandet Sykehus HF Kristiansand Agder Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07205614 on ClinicalTrials.gov ↗ ← All trials in Norway