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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5-18
SponsorUniversity of Colorado, Denver

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Educational Video on Voiding Dysfunction

    Other intervention

    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.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Educational VideoExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Perceived Adherence

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

Time frame
4 weeks, 8 weeks.

Secondary outcomes

1

Video Acceptability

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).

Time frame
0 weeks.
2

Dysfunctional Voiding Scoring System

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.

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

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: