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

Ghent University Hospital (UZ)

Status: Invitation-only

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

Treatments: Other: Semi-structured in-depth interviews with standardized validated questionnaires; Other: Completion of a urological time-line

Study type: Observational

Funder types: Other

Identifiers

NCT07339865

ONZ-2024-0541

Details and patient eligibility

About

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.

Full description

This study investigates the experiences of adolescents with urinary symptoms during the transition from pediatric to adult urological care. This transition is a complex, multidisciplinary process that impacts their well-being and treatment. Gaining insight into the perceptions of and barriers within this transition is crucial for improving care and guidance for future patients.

This mix-method study uses in-depth interviews and standardized questionnaires and focuses on adolescents (16-25 years) with a history of urinary symptoms who are currently being followed for these complaints. Data collection includes a timeline completion of the urological care pathway from birth untill the moment of the interview, semi-structured interviews, and questionnaires. Twenty participants will be included, with the possibility of expanding the sample or terminating recruitment early depending on interim results.

Participants will be recruited via healthcare providers at Ghent University Hospital (UZ Gent) from various departments: urology, pediatric urology, pediatric nephrology, and general practice, as well as through lecture evenings organized by UZ Gent for healthcare providers from peripheral settings (outside UZ Gent) involved in the care of adolescents with urinary symptoms. The informed consent form (ICF) will be provided first-signed by the participant in the case of adults, and, in the case of minors, through an informed assent form (IAF) completed by the participant and an informed consent form (ICF) signed by a parent or legal guardian. Subsequently, appointments for an introductory meeting and interview will be scheduled.

After the introductory meeting, participants will complete a timeline of their urological care pathway from birth to date and will independently collect their childhood growth curves, following instructions provided by the research team. The subsequent interview-if approved by the participant-will be audio-recorded, questionnaires will be completed, and all data will later be pseudonymized in accordance with GDPR guidelines. Interviews may take place at UZ Gent, at a preferred location, or via video consultation.

Enrollment: 20 estimated patients

Sex: All

Ages: 16 to 25 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Trial design

20 participants in 1 patient group

Adolescents and young adults (AYA)

Description:

Adolescents and young adults (AYA) with persisting childhood LUTS, none related to a congenital or neurological disorder.

Treatment:

Other: Completion of a urological time-line

Other: Semi-structured in-depth interviews with standardized validated questionnaires