Study of Transition in Real-life Experiences Affecting Micturition and Well-being in Adolescent Years

NCT07339865 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2026-01-14

No results posted yet for this study

Summary

With this study, we would like to interview 16-25-year-olds who have experienced urinary problems since childhood and who are still experiencing symptoms in young adulthood. The transition from childhood, through puberty, to young adulthood is a time period marked by many psychological ans physiological changes, during which it can be difficult to properly monitor certain symptoms. With this study, we aim to gather opinions and experiences of adolescents and young adults in order to improve urological care for other patients in the future.

Conditions

  • Lower Urinary Tract Symptoms (LUTS)
  • Transition Care
  • Enuresis Nocturnal
  • Adverse Childhood Experiences
  • Genitourinary Issues
  • Constipation
  • Sleep Quality
  • Quality of Life

Interventions

OTHER

Semi-structured in-depth interviews with standardized validated questionnaires

Interviews utilize a semi-structured format, with one researcher conducting all interviews to ensure consistency. A piloted, multidisciplinary-approved interview guide is used to ask open-ended questions exploring adolescent transition experiences.

OTHER

Completion of a urological time-line

Participants complete a blank timeline representing their urological care pathway from birth to the moment of the in-depth interview.

Sponsors & Collaborators

  • University Ghent

    collaborator OTHER
  • University Hospital, Ghent

    lead OTHER

Eligibility

Min Age
16 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-28
Primary Completion
2026-07-31
Completion
2029-12-31

Countries

  • Belgium

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07339865 on ClinicalTrials.gov