Study of Transition in Real-life Experiences Affecting Micturition and Well-being in Adolescent Years
STREAMWAY
Perceptions and Barriers of Transition in Care Among Patients on Pediatric and Adult Urology Services - STREAMWAY: Study of Transition in Real-life Experiences Affecting Micturition and Well-being in Adolescent Years
1 other identifier
observational
20
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 28, 2025
CompletedFirst Submitted
Initial submission to the registry
December 19, 2025
CompletedFirst Posted
Study publicly available on registry
January 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2029
January 14, 2026
December 1, 2025
1.4 years
December 19, 2025
January 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Perceptions, Attitudes, and Experiences Regarding Transition from Pediatric to Adult Urological Care
Assessment of adolescents' perceptions, attitudes, and experiences related to the transition from pediatric to adult urological care, as measured using a semi-structured in-depth interview after or during completion of the transition process, depending of the age of the included participant.
Baseline (single assessment)
Secondary Outcomes (7)
Persisting LUTS in adolescence
Baseline (single assessment)
Constipation complaints
Baseline (single assessment)
Sleep quality
Baseline (single assessment)
Quality of Life reporting
Baseline (single assessment)
Quality of Life - LUTS related
Baseline (single assessment)
- +2 more secondary outcomes
Study Arms (1)
Adolescents and young adults (AYA)
Adolescents and young adults (AYA) with persisting childhood LUTS, none related to a congenital or neurological disorder.
Interventions
Participants complete a blank timeline representing their urological care pathway from birth to the moment of the in-depth interview.
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.
Eligibility Criteria
The Study of Transition in Real-life Experiences Affecting Micturition and Well-being in Adolescent Years (STREAMWAY) aims to map perceptions, attitudes and experiences of adolescents who have undergone the transfer from paediatric to adult urological care. Participants should have received follow-up care for childhood LUTS from a general practitioner, urologist, paediatric urologist, or paediatric nephrologist. At the initial study visit, before enrolment, AYA patients with LUTS undergo a complete diagnostic work-up as part of standard care to determine the presence of LUTS at the time of consultation.
You may qualify if:
- LUTS (according to ICCS definition) present during childhood
- Participants receiving follow-up care for LUTS from a general practitioner, urologist, paediatric urologist, or paediatric nephrologist.
- Individuals aged 16-25 years who have recently transitioned to adult care or are currently undergoing the transition process.
You may not qualify if:
- Patients not comfortable conducting interviews and completing questionnaires in Dutch
- Participants with neurological conditions or congenital anatomical anomalies that may cause LUTS, as these individuals are already followed in established transition pathways and cannot be compared to the target population
- Individuals with cognitive impairments that impair their capacity to independently participate in interviews or complete questionnaires.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Ghentcollaborator
- University Hospital, Ghentlead
Study Sites (1)
Ghent University Hospital
Ghent, East-Flanders, 9000, Belgium
Related Publications (2)
Karamaria S, Mauel R, Van den Ende M, Oosterlinck A, Verheye A, De Bruyne E, Degrauewe E, Dhondt K, Dossche L, Raes A, Renson C, Samijn B, Spinoit AF, Everaert K, Walle JV. Transition in enuresis patients: Identifying the gaps and opportunities for the future. Neurourol Urodyn. 2024 Jun;43(5):1118-1126. doi: 10.1002/nau.25460. Epub 2024 Apr 8.
PMID: 38587243BACKGROUNDVan den Ende M, Joinson C, Sinha S, Verbakel I, Ochoa DC, Lazar J, Baird A, Selai C, Van Huele A, Bou Kheir G, Spinoit AF, Abrams P, Everaert K, Herve F. Navigating the waters of LUTS from childhood to puberty - NOPIA meeting (ICI-RS 2024). J Pediatr Urol. 2025 Dec;21(6):1477-1485. doi: 10.1016/j.jpurol.2025.07.011. Epub 2025 Aug 18.
PMID: 40829984BACKGROUND
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 19, 2025
First Posted
January 14, 2026
Study Start
February 28, 2025
Primary Completion (Estimated)
July 31, 2026
Study Completion (Estimated)
December 31, 2029
Last Updated
January 14, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
Maintaning confidentiality and patient safety. Data is entered manually on an online firewall-protected data registry on the password-encrypted server of Ghent University. Subsequently, data is stored in a central IBM SPSS database also protected by the institutional firewall. Pseudonymized qualitative and quantitative data are registered in separated data sets, accessible to the PI, trial coordinator, and co-investigators. Only the trial coordinator has access to a key file with pseudonymization codes linked to patient data.