Pediatric Locomotor Training Bladder Study

Sponsor
University of Louisville (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03559036
Collaborator
The Leona M. and Harry B. Helmsley Charitable Trust (Other), Kosair Charities, Inc. (Other)
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Study Details

Study Description

Brief Summary

Bladder dysfunction is one of the most important factors influencing duration and quality of life in children with spinal cord injury. Effective bladder control comprises a major aspect of a child's life with SCI and is especially challenging due to the rapid changes in a child's physical and cognitive development. Urological consequences secondary to a neurogenic bladder are responsible for many clinical complications post-spinal cord injury, including repeated urinary tract infections, autonomic dysreflexia, lifelong urologic care, and many hospitalizations. Alternative approaches to bladder management that focus on recovery of function and age-appropriate independence are needed. Prior research findings in our lab in adult participants indicate a benefit of locomotor training on bladder function. The purpose of this study is to determine with quantitative unbiased urodynamic outcome measures if locomotor training, provided to children with spinal cord injury, impacts the developing urinary system.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Locomotor Training

Detailed Description

Our overall hypothesis is that spinal cord injury-induced bladder dysfunction, facilitated by the loss of supra-spinal connections and subsequent alterations of the lumbosacral circuitry, can be ameliorated through activity-based therapy that regulates the state of detrusor-sphincter dyssynergia and normalizes release of neurotrophic factors known to contribute to bladder hyper-reflexia. The primary study aim is to determine the effects of weight-bearing task-specific training for locomotion (stepping on a treadmill) after incomplete and complete spinal cord injury in children on bladder storage, voiding, biomarkers, and quality of life (parent-reported during baseline and exit interview). A secondary aim is to develop a scale for classifying bladder recovery after spinal cord injury based either on the pattern of storage and voiding prior to injury (if the child had bladder control prior to injury) or on established patterns of micturition development (if the child was injured prior to experiencing bladder control).

Study Design

Study Type:
Observational
Anticipated Enrollment :
6 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Impact of Activity-Dependent Plasticity on Bladder Function After Pediatric Spinal Cord Injury
Actual Study Start Date :
Apr 26, 2018
Anticipated Primary Completion Date :
Dec 30, 2022
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Locomotor Training

Assessments for bladder function will be conducted pre-training and following 80 sessions of locomotor training. Locomotor training consists of body-weight supported stepping on a treadmill for one hour.

Procedure: Locomotor Training
Body-weight supported stepping on a treadmill.
Other Names:
  • Step Training
  • Outcome Measures

    Primary Outcome Measures

    1. Bladder Storage [2 years]

      Bladder Capacity

    Secondary Outcome Measures

    1. Bladder Emptying [2 years]

      Voiding Efficiency

    2. Bladder Pressure [2 years]

      Leak Point and Maximum Pressure

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    2 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Supra-sacral, non-progressive spinal cord injury

    • Bladder dysfunction post-injury

    Exclusion Criteria:
    • Use of anti-spasticity medications or unwillingness to wean off of medications

    • Botox (onabotulinumtoxinA) in the bladder within 9 months of the study

    • Bladder dysfunction or urinary tract impairment prior to injury

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Louisville Louisville Kentucky United States 40202

    Sponsors and Collaborators

    • University of Louisville
    • The Leona M. and Harry B. Helmsley Charitable Trust
    • Kosair Charities, Inc.

    Investigators

    • Principal Investigator: Charles Hubscher, PhD, University of Louisville

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Charles Hubscher, Professor, University of Louisville
    ClinicalTrials.gov Identifier:
    NCT03559036
    Other Study ID Numbers:
    • 17.1007
    First Posted:
    Jun 15, 2018
    Last Update Posted:
    May 10, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Charles Hubscher, Professor, University of Louisville
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 10, 2022