Recruiting

Observational Study

Sponsor:

University of Wisconsin, Madison

Code:

NCT06966375

Conditions

Hypospadias

Eligibility Criteria

Sex: Male

Age: 5 - 65

Healthy Volunteers: Not accepted

Interventions

WYSH Web Application

Study Details

Brief summary:

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.

Conditions

Hypospadias

Study ID

NCT06966375

Start date

Jul 23, 2025

Status verified date

Mar, 2026

Completion date

Nov, 2026

Anticipated

Primary completion date

Nov, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 5 - 65

Healthy Volunteers: Not accepted

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:

\-

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Male Participants with Repaired Hypospadias

  • 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

Interventions

WYSH Web Application

Worldwide Yearly Screening for Hypospadias (WYSH) Web Application

Primary outcome measure

  • 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 ]

Central Contacts and Locations

Locations

UW School of Medicine and Public Health

Recruiting

Madison, Wisconsin, United States, 53792

More Information

Sponsor

University of Wisconsin, Madison

Last update posted

Mar 27, 2026

Last verified

Mar, 2026

Keywords

  • Hypospadias Complications
  • Quality of Life
  • Patient-Reported Outcomes

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Wisconsin, Madison on 2026-03-27.