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Clinical Trials in Germany / NCT06912594
Starting soon Not applicable

App Impact on Quality of Life and Symptoms in PCOS

NCT06912594 · tracked via the Priya Life Science Germany tracker
Sponsor
Endo Health GmbH
Phase
Not applicable
Started
2025-04-02
Last updated
2025-04-06

Condition(s) studied

Polycystic Ovary Syndrome (PCOS)

Investigational drug(s) / intervention(s)

PCOS-App

PCOS-App: The PCOS-App helps to implement multimodal self-help measures in the daily lives of PCOS patients through various functions such as symptom diary and interactive exercises.

Study summary

This study investigates the influence of a PCOS app on the quality of life and symptoms of individuals with polycystic ovary syndrome (PCOS). The intervention group can use the app over the study period of twelve weeks in addition to care-as-usual (CAU). In the control group, this is compared with no use of the PCOS-App for a twelve-week period, that is, care-as-usual only/ continuation of the current treatment (waitlist design). The aim is to evaluate the effectiveness of the app and to gain insights for the design of future studies. The study is expected to last seven months and include 220 participants.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Legal capacity * Resident in Germany * Female gender * Age ≥18 years up to 65 years * Diagnosed and medically confirmed Polycystic Ovary Syndrome (E28.2) * Ownership of a smartphone with a compatible iOS or Android version and the ability to operate it * Internet access and an email address for registration, app usage, and completing questionnaires * Willingness to complete questionnaires online * Motivation to use the app regularly * Sufficient knowledge of the German language Exclusion Criteria: * Changes in hormone therapy within eight weeks prior to the start of the study and/or planned within the next 12 weeks * Changes in treatment with metformin within eight weeks prior to the start of the study and/or planned within the next 12 weeks * Current treatment with medications for obesity (e.g., liraglutide, orlistat) * Changes in treatment with anti-androgens (e.g., spironolactone, cyproterone acetate, flutamide) within eight weeks prior to the start of the study and/or planned within the next 12 weeks * Pregnancy or breastfeeding * Current hormonal fertility treatment * Changes in treatment with psychotropic medications within eight weeks prior to the start of the study and/or planned within the next 12 weeks * Current psychotherapeutic treatment * Previous or current access to the Endo-App or other digital health applications (DiGAs) * Current participation in other clinical studies * Current nutritional counseling according to §20 SGB V or nutritional therapy according to §43 SGB V, or participation in weight reduction programs

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Endo Health GmbH Chemnitz Saxony

More Endo Health GmbH trials in Germany

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 NCT06912594 on ClinicalTrials.gov ↗ ← All trials in Germany