N/A
N=4
Toilet Training Toddlers and Preschoolers
Incontinence · Enuresis
Bottom Line
View on ClinicalTrials.gov: NCT01747343 ↗Enrolled (actual)
4
Serious AEs
0.0%
Results posted
Sep 2014
Primary outcome: Primary: Change in the Mean Number of Accidents Across Children — -1.3 Accidents
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Underwear/Differential Reinforcement (Behavioral)
- Age
- Pediatric, Adult, Older Adult · 0+ yrs
- Sex
- All
- Sponsor
- University of Kansas
- Primary completion
- Jul 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in the Mean Number of Accidents Across Children |
-1.3 | — |
| SECONDARY Change in the Mean Percentage of Appropriate Eliminations Across Children |
33.4 | — |
Summary
The investigators are interested in determining those procedures that prove to be most efficient and effective in facilitating continence (i.e., "dry pants" or the absence of soiled undergarments), appropriate eliminations (i.e., voids/stools in toilet), and independent requests/initiations to use the toilet. To assess the effectiveness of toilet training methods (procedures), data on toileting skills (in addition to each skill in a given child's curriculum) are collected across the school day (7:30 am-5:45 pm) by the classroom teachers. The primary dependent variables (toileting skills) are continence (i.e., absence of soiled undergarments), appropriate eliminations (i.e., the number of voids/stools made in the toilet), and independent/self requests (i.e., communication by the child with an adult to use the toilet). The toileting procedures are implemented by classroom teachers (undergraduate practicum students) and implementation is monitored by classroom supervisors (graduate teaching assistants). Procedural effectiveness is evaluated on a daily basis by the graduate teaching assistants and on an at-least-weekly basis by faculty supervisors.
Eligibility Criteria
Inclusion Criteria
- Individual not yet toilet trained
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT01747343). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.