Worldwide Yearly Screening for Hypospadias
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: WYSH Web Application.
- Who it may be relevant to
- Registry conditions: Hypospadias. Basic parameters: 5 years — 65 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Pilot Testing of the Worldwide Yearly Screening for Hypospadias
Overview
The purpose of this study is to recruit approximately 20 male participants who have a history of repaired hypospadias to test the feasibility and acceptability of the Care Planning Tool within the Worldwide Yearly Screening for Hypospadias (WYSH) Web Application.
Detailed description
Several studies show that patients who undergo hypospadias repair report significant functional and psychosexual issues in adolescence or adulthood (in more than 50% of cases). The Care Planning tool within the Worldwide Yearly Screening for Hypospadias (WYSH) Web Application, developed using expert level consensus from a Delphi Measure including stakeholders (psychologists, urologists, endocrinologists, patients/families), is designed to support the functional and psychosexual health of male youth and adults treated for hypospadias, to support their physical and mental health after repair.
This is a pilot study of the WYSH intervention to access its feasibility and acceptability.
\[Potential participants can enroll at their local clinic.\]
Interventions
- Other WYSH Web Application
Worldwide Yearly Screening for Hypospadias (WYSH) Web Application
Primary outcome measures
- Feasibility: Participant Count to Summarize answers of the Care Planning Tool [Time frame: Baseline, 3 weeks, 3 months]
- Acceptability: User Centered Metrics [Time frame: Baseline, 3 weeks, 3 months]
- Acceptability: Cognitive Debriefing Measures [Time frame: Baseline, 3 weeks, 3 months]
- Feasibility: System Usability Testing [Time frame: Baseline, 3 weeks, 3 months]
Secondary outcome measures (1)
- Provider Acceptability: Usability Scale [Time frame: Data collected after participating patient completes questionnaire, up to approximately 3 months.]
Eligibility criteria
Inclusion criteria
- Males who have a documented history of repaired hypospadias.
- Age groups targeted, based on recommended standards for user experience data from pilot studies:
- 3-5 Males, age 5-10 (with parental consent and child assent)
- 3-5 Males, age 11-15 (with parental consent and child assent)
- 3-5 Males, age 16-20 (with parent consent, child assent until age 18)
- 3-5 Males, age 21-65
Exclusion criteria
\-
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- UW School of Medicine and Public Health — Madison
Identifiers
NCT: NCT06966375 · 2025-0402 · 2K12DK100022-06 · A539800 · Protocol Version 3/16/26