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NCT Number: NCT06909552

Use of an Educational Video to Improve Adherence to Treatment in Voiding Dysfunction

This study aims to see whether an educational video on a common urinary dysfunction leads to improved parent and child perceived adherence to treatments recommendations.

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Key information

Age range

5 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Colorado Anschutz

Aurora, Colorado, 80045, United States

Location contact

Jennifer Pyrzanowski

CONTACT

[email protected]

303-724-0769

About this study

This study aims to explore whether the use of an educational video on voiding dysfunction, a common urinary dysfunction, leads to improve parents and child perceived adherence to behavioral treatment recommendations. Our main hypothesis explores whether there is improved perceived adherence, and whether this improved perceived adherence leads to better symptom outcomes in this condition.

We do so through randomizing patients to a control and intervention group, where the latter is exposed to the educational video, while the control group experiences standard of care visits/follow-ups. Data is collected through surveys pre and post exposure to the intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Parents and Caregivers of pediatric urology patients with a diagnosis of Dysfunctional voiding (minimum 100 participants)
  • 5-18 years old, no younger than 5 and no older than 18 years old
  • Potty-trained - fully independent with toileting, can complete every step of the process and can do so satisfactorily by themselves.

Exclusion criteria

  • Children with Voiding dysfunctionDysfunctional voiders with medically complex conditions (neurogenic bladder, POTS, EDS, etc.)
  • Parent's child is notNot a first-time patient (i.e. has been seen in the past for dysfunctional voiding)
  • Child has severeSevere intellectual disability, developmental delay, or cognitive impairment.

Treatment and study plan

Educational Video on Voiding Dysfunction

Other

The educational video is a short 3-minute video which describes the condition in detail, at the level that a parent or child could understand without a medical background.

Primary outcomes

  1. Perceived Adherence

    Time frame: 4 weeks, 8 weeks.

    Participants will take the TAPQ perceived adherence assessment at time points 4 weeks and 8 weeks.

Secondary outcomes

  1. Video Acceptability

    Time frame: 0 weeks.

    Immediately after watching the educational video, participants will be asked to complete a questionnaire on the acceptability of the video. this will occur at time frame 0 weeks (for intervention group).

  2. Dysfunctional Voiding Scoring System

    Time frame: 0 weeks, 4 weeks, and 8 weeks.

    Participants will be asked to complete a DVSS survey at timepoints 0 weeks, 4 weeks, and 8 weeks. This DVSS survey will be used to assess symptom improvement throughout the study.

Study contacts

Contact information is provided by the study sponsor or research team.

Jen Pyrzanowski

CONTACT

[email protected]

Marguerite Korber, CPNP

CONTACT

[email protected]

720-777-6523

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Registry information

Official study title

Use of an Educational Video to Improve Caregiver Knowledge, Adherence to Recommendations, and Outcomes in Children With Dysfunctional Voiding

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Apr 3, 2025
Registry last updated
Jul 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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