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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05528601
Other study ID # Pre ELEA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date January 30, 2022

Study information

Verified date August 2022
Source University Hospital Muenster
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of quality of life before and after 14 days of use of Endo App® in endometriosis patients compared to non-users


Description:

Introduction: Endometriosis can significantly impair the quality of life of those affected. Multimodal self-help measures are recommended but often difficult to access. Smartphone apps have been shown to improve quality of life for other conditions with chronic pain. The aim of this study was to examine whether there is evidence of beneficial effects of the Endo-App and whether a multicenter randomized controlled trial should be planned to substantiate these effects. Methods: In a sample of N=106 women affected by endometriosis the present study determined the influence of the use of a smartphone app (Endo-App ®) on their quality of life. Among others, the validated questionnaire Endometriosis Health Profile from Oxford University was used for this purpose.


Recruitment information / eligibility

Status Completed
Enrollment 106
Est. completion date January 30, 2022
Est. primary completion date January 15, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - suffering from endometriosis - 18 years or older - willing and capable of using a smartphone Exclusion Criteria: - minor under 18 years - endometriosis excluded - not capable of using a smartphone

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
use of Endo App®
use of Endo App® smartphone application containing endometriosis relevant exercises and educational material

Locations

Country Name City State
Germany University Hospital Münster Germany Münster NRW

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Muenster

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary quality of life of endometriosis patients quality of life measured bei Endometriosis Health Profile 30 14 days
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