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Individualized Assessment of Motor Function and Balance in Intensive Therapy

Active, not recruiting
Conditions
Neurodevelopmental Disorders
Registration Number
NCT05820412
Lead Sponsor
University of Missouri-Columbia
Brief Summary

The goal of this study is to assess the individualized use of technology to assess motor function and balance for ambulatory children participating in an intensive therapy episode of care and determine the effectiveness of the program. Children 7-17 years old who can walk and are completing an intensive therapy episode of care will be recruited to participate in this study. Demographic, health history, and PT,OT,ST medical records will be collected. Based on the participant's functional goals, motor function and balance tests will be selected including common balance tests (standing with eyes open, standing with eyes closed), walking, walking and turning, standing up and sitting down from a bench, reaction time, and step down. Participants will be tested before, immediately after, 6 weeks after, and 12 weeks after the episode of care.

Detailed Description

The goal of this study is to assess the individualized use of instrumented assessment of motor function and balance for ambulatory children participating in an intensive therapy episode of care and determine the effectiveness of the intervention. Children 7-17 with neurodevelopmental diagnosis, GMFCS Levels I and II and completing an intensive therapy episode of care will be recruited to participate in this study. Demographic, health history, and PT,OT,ST medical records will be collected. Based on the participant's functional goals, motor function and balance tests in single and dual conditions will be selected including Romberg balance tests, walking, walking and turning, sit to/from stand, reaction time, and step down administered while participant is recorded using a portable measurement platform which incorporates a custom force plate, Azure Kinect spatial sensor, and interface board. Participants will be tested before, immediately after, 6 weeks after, and 12 weeks after the episode of care. Testing is estimated to last for 45 minutes.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Ambulatory children 7-17 years old receiving care in an interdisciplinary, intensive therapy program
  • GMFCS Levels I and II
  • able to follow 2-3 step directions
  • English speaking
Exclusion Criteria
  • orthopedic surgery in the past year or
  • significant visual impairment
  • significant hearing impairment.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Eyes closed standing on firm surface12 weeks following physical therapy

joint kinematics (movement strategies) obtained while eyes closed standing on firm surface

Walking12 weeks following physical therapy

stride length obtained from spatial sensor

5 Times sit to stand test12 weeks following physical therapy

knee joint kinematics obtained from spatial sensor

Step down12 weeks following physical therapy

knee joint kinematics obtained from spatial sensor

Secondary Outcome Measures
NameTimeMethod
Measures of processes of careimmediately following the episode of care

Questionnaire designed to assess parents' perceptions of the care they and their children receive from children's rehabilitation treatment centres. It is a means to assess family-centred behaviours of health care providers.

Trial Locations

Locations (1)

Children's Therapy Center--MU Healthcare

🇺🇸

Columbia, Missouri, United States

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