A feasibility study on a smartphone treatment application for psychogenic erectile dysfunctio
Not Applicable
- Conditions
- Psychogenic erectile dysfunction
- Registration Number
- JPRN-UMIN000047183
- Lead Sponsor
- Waseda University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Male
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
Those meeting any of the items below. 1. Those receiving or attending any other psychological treatment or clinical trials. 2. Those with a diagnosis of hypertensive disease, heart disease (excluding hypertensive), cerebrovascular disease, chronic kidney disease, or diabetes mellitus. 3. Those with suspicions of alcohol or drug abuse. 4. Those whose participation judged inappropriate for any other reason by their primary care physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in the IIEF-15 score from pre- to post-8 week and at the 1-month, 3-month, and 6-month follow-ups
- Secondary Outcome Measures
Name Time Method