- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06305689
Defining Treatment Outcomes and Genetic Architecture in Idiopathic Toe Walking* (ITW)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Sacramento, California, United States, 95817
- Shriners Hospitals for Children
-
-
Illinois
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Chicago, Illinois, United States, 60707
- Shriners Hospitals for Children
-
-
Kentucky
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Lexington, Kentucky, United States, 40508
- Shriners Hospitals for Children
-
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Oregon
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Portland, Oregon, United States, 97239
- Shriners Hospitals for Children
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19140
- Shriners Hospitals for Children
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South Carolina
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Greenville, South Carolina, United States, 29605
- Shriners Hospitals for Children
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Utah
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Salt Lake City, Utah, United States, 84103
- Shriners Hospitals for Children
-
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Washington
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Spokane, Washington, United States, 99204
- Shriners Children's Spokane
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosis of Idiopathic Toe Walking Persistent (ITWp)
- Between the ages of 6-18 years
- Passive dorsiflexion dorsiflexion with knee extension between -10 plantar flexion - + 5 degrees of dorsiflexion, DiGiovanni defined an isolated gastrocnemius contracture as maximum passive ankle dorsiflexion as < 5 degrees with the knee in full extension
Exclusion Criteria:
- Diagnosis of Autism or autism spectrum disorder
- Presence of any indicators of trauma, neuromuscular influence or neurogenic influence as identified by using the Toe Walking Tool
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Serial Casting
Repeated casts weekly until desired dorsiflexion range achieved
|
Repeated casts weekly until desired dorsiflexion range achieved
|
|
Active Comparator: Surgery
Surgical procedure to the gastrocnemius and/or plantar fascia
|
Surgical procedure to the gastrocnemius and/or plantar fascia
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gait parameters: Velocity
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Velocity (m/s) will be assessed during walking in the gait lab.
|
Baseline, 6 months post intervention, 1 year post intervention
|
|
Three dimensional Gait Analysis:Kinematics (degrees)
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Kinematics as calculated from the reflective markers placed on the skin during the computerized gait analysis will allow for the computation of knee, ankle and foot kinematics during walking. Knee Kinematics (measured in degrees): Knee angle at IC, knee extension at midstance, peak knee flexion in swing. Ankle kinematics (measured in degrees): Ankle angle at IC, ankle angle at midstance, angle range of 3rd rocker, average ankle angle in stance, average ankle angle in swing. Multisegment Foot Motion (measured in degrees): ankle complex flexion, rotation, 2)midfoot flexion, rotation and 3) hallux varus and flexion rotation. |
Baseline, 6 months post intervention, 1 year post intervention
|
|
Dynamic Motor Control Index during Walking (Walk-DMC)
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Walk-DMC is a measure of motor control which is calculated from the dynamic muscle activity from five muscles (rectus femoris, medial and lateral hamstrings, tibialis anterior and gastrocnemius, bilaterally)
|
Baseline, 6 months post intervention, 1 year post intervention
|
|
Three dimensional Gait Analysis:Kinetics (nm/kg)
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Ankle kinetics: peak plantarflexion moment and power absorption at loading response, power generation at terminal stance will be calculated from the force plates and gait kinematics during the walking gait analysis.
|
Baseline, 6 months post intervention, 1 year post intervention
|
|
Quantitative Assessment of Toe Walking
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Quantitative assessment of toe walking will be obtained with the in-shoe system the NURVV/RUN.
The NURVV/RUN calculates the percentage of foot contact time spent on the rearfoot, midfoot and forefoot.
|
Baseline, 6 months post intervention, 1 year post intervention
|
|
Pediatric Outcomes Data Collection Instrument
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Daily functional musculoskeletal health will be assessed with the Pediatric Outcomes Data Collection Instrument, a questionnaire that contains 108 questions in seven domains including four functional assessment areas: upper extremity functioning, transfers and basic mobility, sports and physical function, and comfort/pain.
Items have different weights, with possible scores range from three (often, sometimes, rarely or never) to five (none, very mild, moderate, severe, very severe).
For most items a lower score indicates higher functioning or a more positive quality of life.
|
Baseline, 6 months post intervention, 1 year post intervention
|
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Gait Parameters:Stride Length (m)
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Stride Length (m) will be assessed during walking in the gait lab.
|
Baseline, 6 months post intervention, 1 year post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Passive Range of Motion
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
Dorsiflexion with and without knee flexion, popliteal angle are measured with a goniometer and measured in degrees
|
Baseline, 6 months post intervention, 1 year post intervention
|
|
Muscle Strength
Time Frame: Baseline, 6 months post intervention, 1 year post intervention
|
A hand-held dynamometer (HHD) will be used to assess quantitative muscle strength, via a "make test" for ankle dorsiflexors/plantarflexors, and foot inverters/everters, bilaterally.
|
Baseline, 6 months post intervention, 1 year post intervention
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coactivation Tool
Time Frame: Baseline
|
The coactivation tool utilizes electromyographic activity during two lower extremity activities to determine whether there is coactivation between the gastrocnemius and the quadriceps during resistive knee extension bilaterally.
Abnormalities in the muscle activation pattern may be an indication of a diagnosis other than idiopathic toe walking.
|
Baseline
|
|
Bruininks-Oseretsky Test of Motor Proficiency (BOT-2)
Time Frame: Baseline
|
The subtests of Bilateral Coordination and Balance which form the Body Coordination composite score will be used ascertain coordination of children with ITW relative to age-matched norms to help characterize the population and determine if coordination influences outcome.
Higher scores indicate better balance and bilateral coordination.
|
Baseline
|
|
Genomics
Time Frame: Baseline
|
Whole Genome Sequencing will be done on the participant and both biological parents (if possible) to determine if the patient and their parents have any genetic abnormalities in genes that may be associated with toe walking and to determine if the cohort as a whole have potential new genes that may be indicative of toe walking.
|
Baseline
|
|
Selective Motor Control
Time Frame: Baseline
|
Selective Voluntary Motor Control Scale is a simple clinical measure of the ability to selectively control the muscles.
Selective motor control of the hip, knee, ankle, subtalar, and toe joints will be assessed using the Selective Voluntary Motor Control tool.
A total of 10 points is possible for each side with higher numbers indicating more selective control.
|
Baseline
|
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The Toe Walking Tool
Time Frame: Baseline
|
This novel tool designed for screening out children who toe walk for other reasons such as neurogenic, neuromuscular, or traumatic.
If any questions are answered as yes, the principal investigator will review to determine whether a diagnosis of idiopathic toe walking is appropriate.
|
Baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jeremy Bauer, MD, Shriners Hospitals for Children-Portland
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 79144
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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