RecruitingEndometriosis
MY-ENDO -- Mind Your ENDOmetriosis: a Digital Mindfulness- and Acceptance-based Endometriosis Self-management Program
Eligible age
18+ yrs
Accepts
Women
Locations
0 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
The purpose of the study is to assess the effect of a digital mindfulness- and acceptance-based psychological intervention on quality of life, work ability, pain experience and physical and mental health in participants experiencing chronic pain, fatigue and/or reduced quality of life due to endometriosis.
Sponsor: University of Aarhus
You may qualify if…
- ✓ ≥18 years old.
- ✓ Signed informed consent.
- ✓ Endometriosis diagnosed by a gynecologist based on the medical case history, ultrasound, laparoscopy, or MRI (all self-reported).
- ✓ Moderate to severe symptoms (pelvic pain and/or fatigue measured on an 11-point numeric rating scale (NRS) from 0 = no pain/fatigue to 10 = worst imaginable pain/fatigue symptom) or reduced endometriosis-related quality of life (measured by the EHP-30):
- ✓ Moderate to severe endometriosis-related chronic pelvic pain (NRS \> 2) or
- ✓ Moderate to severe endometriosis-related fatigue (NRS \> 2) or
- ✓ Low endometriosis-related quality of life (one or more EHP-30 subscale mean scores ≥ 40.00).
- ✓ Relevant clinical and/or surgical treatment according to the European Society of Human Reproduction and Embryology (ESHRE) guidelines for endometriosis has been attempted.
You may not qualify if…
- ✕ Under 18 years old.
- ✕ Severe psychiatric diagnosis made by a psychiatrist and/or ongoing psychiatric treatment.
- ✕ Pregnancy or planned pregnancy during the study period.
- ✕ An estimated lack of capacity or surplus energy to enter into a digital mindfulness treatment, for instance, because of:
- ✕ major life events taking place at the same time (e.g., divorce, loss of a close relative, etc.)
- ✕ linguistic or cultural barriers
Source: ClinicalTrials.gov · NCT06211231 · last updated 2024-04-03