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Worldwide Yearly Screening for Hypospadias (WYSH)

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Enrolling

Conditions

Hypospadias

Treatments

Other: WYSH Web Application

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06966375
A539800 (Other Identifier)
Protocol Version (Other Identifier)
2025-0402
2K12DK100022-06 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

20 estimated patients

Sex

Male

Ages

5 to 65 years old

Volunteers

No Healthy Volunteers

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

-

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Male Participants with Repaired Hypospadias
Experimental group
Description:
* 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
Treatment:
Other: WYSH Web Application

Trial contacts and locations

1

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Central trial contact

Haley Bryte

Data sourced from clinicaltrials.gov

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