CeRa Münster, Centre of Reproductive Medicine and Andrology
Münster, Germany, 48149
NCT Number: NCT06501144
The goal of this observational study is to assess the long-term effectiveness of a digital health application for treating erectile dysfunction in men aged 18 and older. The main questions it aims to answer are:
* Will participants maintain an improvement of their erectile function, that means maintain an improvement of at least 3 points in the IIEF-5 score at 3 months post-therapy? * How does the application affect overall health status and disease-related quality of life?
Participants will:
* Complete validated questionnaires (IIEF-5, PGI-I, QOL-Med) to track erectile function, overall health status, and quality of life at up to two follow-up points after using the app with a 3-month self-management program combining cardiovascular training, pelvic floor exercises, psychological support, and educational content. * Provide information on demographics, risk factors, and other relevant health characteristics for subgroup analysis.
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Notify Me18 year and older
Male
Observational
Münster, Germany, 48149
The intervention that needs to be completed prior participation in this study involves a digital therapy program delivered via a smartphone or tablet application. This program includes several components aimed at addressing different aspects for the treatment of erectile dysfunction:
Overall, the digital therapy program is designed to provide comprehensive support for men with erectile dysfuntion, addressing both physical and psychological aspects of the condition to improve symptom severity, quality of life, and patient activation.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 6 months after start of the app-based therapy
The primary endpoint is the rate of patients maintaining an IIEF-5 score improvement of ≥ 3 points compared to baseline (start of app-based therapy) after the app-based therapy
Time frame: 6 months after start of the app-based therapy
Assessment of overall improvement of patients' health status using the PGI-I questionnaire
Time frame: 6 months after start of the app-based therapy
Assessment of disease-related quality of life using the QOL-Med questionnaire
Time frame: 6 months after start of the app-based therapy
•. PGI-I
Derived variables
Kranus Health GmbH
Industry
Acronym: RELOED
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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