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Effects of Soft Tissue Lengthening on Gait in Children With Spasticity

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Muscle Spasticity

Treatments

Procedure: selective percutaneous muscle release

Study type

Observational

Funder types

Other

Identifiers

NCT04090892
STU 042014-068

Details and patient eligibility

About

This research project is being conducted to investigate changes in secondary impairments, functional mobility skills, and gait variables in children with spasticity following selective percutaneous myofascial lengthening. The research project proposed here will be the first to use instrumented three-dimensional motion analysis to investigate the effects of selective percutaneous myofascial lengthening on gait kinematics and kinetics. The objectives of the study are to:

  1. Compare gait kinematics and kinetics in children and young adults with lower extremity spasticity before and after selective percutaneous myofascial lengthening to determine the effects of this procedure on functional mobility.
  2. Identify changes in impairments and activity limitations following selective percutaneous myofascial lengthening .
  3. Identify changes in a family or caregivers perceived quality of life after their child's selective percutaneous myofascial lengthening .

The aim of this study is to identify and describe the specific changes in secondary musculoskeletal impairments, activity limitations, and gait kinematics and kinetics after a selective percutaneous myofascial lengthening procedure. Gait kinematics and kinetics includes the motion of joints and body segments, and force and power, at each lower extremity joint, respectively. The results of this study will provide preliminary information on how this form of soft tissue lengthening affects functional mobility skills in children with spasticity. The study is expected to run for two years and the primary study endpoint is when participants have completed their second post- operative data collection session.

Enrollment

8 patients

Sex

All

Ages

4 to 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Scheduled for an selective percutaneous myofascial lengthening procedure,
  • Between the ages of 4.0 and 20.11 years old,
  • Lower extremity spasticity,
  • Able to ambulate 50 feet without a rest, with or without an assistive device, and with or without ankle foot orthoses (AFOs) and
  • Able to follow one step directions.

Exclusion criteria

  • Botox injections into any lower extremity muscle within three months of the scheduled selective percutaneous myofascial lengthening procedure,
  • Lower extremity orthopedic surgery within 6 months of the scheduled selective percutaneous myofascial lengthening procedure,
  • Visual impairment that interferes with maintaining a straight path while ambulating,
  • Uncontrolled seizure disorder
  • A change in medication that affects spasticity or ability to follow one step directions within three months of the scheduled selective percutaneous myofascial lengthening procedure.

Trial design

8 participants in 1 patient group

Persons with spasticity 4.0-20.11 years
Description:
Study personnel are not carrying out the surgical intervention but are assessing the outcomes of the surgery on gait and motor function.
Treatment:
Procedure: selective percutaneous muscle release

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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