The Effect of an App-based Intervention on Quality of Life in Patients With Endometriosis.
Recruiting · NCT06821217 · Interventional (participants receive a specific treatment) · Lead sponsor: Insel Gruppe AG, University Hospital Bern
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
The goal of this clinical trial is to learn if an App-based intervention affects the quality of life in patients with suspected or confirmed endometriosis. The main questions it aims to answer are: * Does the App-based intervention improve the quality of life? * Does it lead to pain relief? Researchers will compare participants using the App to a control group to see if the App works to improve quality of life and endometriosis-related symptoms. Participants will: * Use an App-based intervention or be in the control group (no App-use) for 6 months * Visit or have a telephone consultation after 3 and 6 months * Complete a questionnaire to assess the quality of life at inclusion, after 1, 3 and 6 months
Who can take part
Inclusion criteria
- Informed Consent as documented by signature
- Age 18 or older
- Premenopausal status (menopause is defined as amenorrhea lasting one year or longer)
- Endometriosis, confirmed by surgery or clinically suspected
- Possession of a smartphone
Exclusion criteria
- Planned endometriosis surgery or planned hormonal therapy in the study period
- Surgery and/or new hormonal therapy in the last three months
- Malignant diseases
- Pregnancy
- Breastfeeding
- Active desire for pregnancy in the study period
- Fertility treatment
- Simultaneous participation in other intervention studies
Where it is running
1 location listed.
- Department of Gynecology and Obstetrics, Women's University Hospital, Inselspital Bern, University of Bern - Bern, Switzerland