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Qol Following Management for Pediatric UI

U

University of South Dakota

Status

Completed

Conditions

Quality of Life
Incontinence

Treatments

Behavioral: Physical Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04867876
QOL after UI treatment

Details and patient eligibility

About

A comparison of changes between symptoms of incontinence and pediatric quality of life will be used to draw conclusions about whether differences in quality of life are noted with changes in symptoms of incontinence.

Full description

Although positive physiological results are associated with successful treatment for bowel and bladder dysfunction and daytime incontinence (BD-UI), there are few studies examining the effects of treatment on quality of life (QoL) for children. The purpose of our study is to determine whether successful physical therapy treatment improves QoL for children with BD-UI.

Consent will be obtained from parents and assent from children. Children will be asked to complete a global, age appropriate quality of life assessment and a quality of life instrument specific to incontinence. Information will be provided by the parent through completion of a parent report instrument matched to the child's global quality of life tool as well as completion of an instrument depicting child symptoms. Clinicians will report general information about related physiological changes and progress with established outcomes individualized to the child. A repeated measures MANOVA will be used to analyze the results.

Enrollment

6 patients

Sex

All

Ages

5 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Children between ages 5-18 who were currently receiving conservative treatment for daytime UI with or without constipation or encopresis met inclusion criteria.

Exclusion criteria

  • Exclusion criteria included children who only had nocturnal enuresis or children with neurogenic bladders.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

6 participants in 1 patient group

Intervention Cohort
Experimental group
Description:
Physical Therapy
Treatment:
Behavioral: Physical Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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