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CompletedNCT04891328Updated Mar 28, 2022

Experience With a Pediatric Summer Intensive Therapy Program

An observational study in Neurodevelopmental Disorders, sponsored by University of Missouri-Columbia. Completed at 1 site in United States. Open to participants aged 4 Years to 15 Years. Per ClinicalTrials.gov, last updated 2022-03-28.

Sponsored by University of Missouri-Columbia · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
13
Ages
4 Years to 15 Years
Sex
All
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Study summary

The purpose of this study is to explore the lived experiences of children with neurodevelopmental diagnoses and their caregivers with an intensive model of therapy. Children will receive usual care during the summer intensive program and the investigators will access medical records to assess effectiveness. Children and caregivers will also be asked to participate in semi-structured interviews upon the completion of the episode of care.

Read the detailed description

The purpose of this study is to explore the lived experiences of children with neurodevelopmental diagnoses and their caregivers with an intensive model of therapy. Research questions include: 1.) What are the perceptions of children and caregivers about intensive therapy after participating in multiple intensive therapy episodes over time? 2.) Why do caregivers choose to continue with an intensive model of therapy periodically for their child with neurodevelopmental diagnoses? 3.) What were the outcomes for children with neurodevelopmental disabilities participating in an episode of intensive therapy? Children will receive usual care during the summer intensive program and the investigators will access medical records to assess effectiveness. Children and caregivers will also be asked to participate in semi-structured interviews upon the completion of the episode of care.

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Conditions studied

  • Neurodevelopmental Disorders

Keywords

  • pediatric rehabilitation
  • intensive therapy
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In context

Neurodevelopmental Disorders

332 studies on the registry are indexed under Neurodevelopmental Disorders; 143 are open to participants now.

This study's enrollment of 13 is below the median of 200 across 124 observational studies indexed under Neurodevelopmental Disorders.

Browse Neurodevelopmental Disorders studies →

Lead sponsor

University of Missouri-Columbia is the lead sponsor of 357 studies on the registry; 70 are open to participants now.

Of its 42 completed or terminated interventional studies of FDA-regulated products, 28 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
4 Years to 15 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children 4-15 years old with neurodevelopmental diagnoses and scheduled for an intensive therapy program over the summer.

Inclusion criteria

  • Children receiving therapy through the Children's Therapy Center's Tiger Intensive Program and their caregivers from May 24 to August 13 2021.

Exclusion criteria

Exclusion Criteria:

  • n/a
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
13 participants (actual)
Patient registry
No

Interventions

  • OtherIntensive therapy program

    The intensive therapy program consists of physical therapy, occupational therapy, and speech therapy 3-6 hours x 4-5 days/week for 4 weeks. The individual therapies received will vary with the child/caregiver goals and be based on neuroplasticity and motor learning principles.

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What researchers measure

Primary outcomes

  1. Semi-structured interviews

    Upon completion of the program, children and caregivers will participate in an interview about their experience

    Time frame: at discharge assessed up to 10 days

  2. Canadian Occupational Performance Measure

    Individualized client-centered performance measure

    Time frame: measured at discharge 4 weeks after enrollment

Secondary outcomes

  1. Change in Lower extremity passive range of motion

    Measured at ankle, knee, and hip with goniometer

    Time frame: Measured at day 1 and discharge 4 weeks later

  2. Change in Thomas Test

    Hip flexor length test

    Time frame: Measured at day 1 and discharge 4 weeks later

  3. Change in popliteal angle

    Hamstring length test

    Time frame: Measured at day 1 and discharge 4 weeks later

  4. Change in Gastrocnemius muscle length

    Measured with goniometer

    Time frame: Measured at day 1 and discharge 4 weeks later

  5. Change in Kids Bestest

    Balance measure for pediatric patients

    Time frame: Measured at day 1 and discharge 4 weeks later

  6. Change in m-CTSIB

    Balance measure

    Time frame: Measured at day 1 and discharge 4 weeks later

  7. Change in Early Clinical Assessment of Balance

    Balance measure

    Time frame: Measured at day 1 and discharge 4 weeks later

  8. Change in Segmental Assessment of Trunk Control (SATCO)

    Measurement of trunk control

    Time frame: Measured at day 1 and discharge 4 weeks later

  9. Change in Edinburgh Visual Gait Scale

    Observational Gait measure

    Time frame: Measured at day 1 and discharge 4 weeks later

  10. Change in Timed Up and Down Stairs

    Measure of stair performance

    Time frame: Measured at day 1 and discharge 4 weeks later

  11. Change in Timed on and off the floor

    Measure of transition from floor to standing

    Time frame: Measured at day 1 and discharge 4 weeks later

  12. Change in 6 minute walk test

    Measure of walking performance

    Time frame: Measured at day 1 and discharge 4 weeks later

  13. Change in Peds QL

    Pediatric quality of life measure

    Time frame: Measured at day 1 and discharge 4 weeks later

  14. Change in GOAL

    patient reported measure of function mobility

    Time frame: Measured at day 1 and discharge 4 weeks later

  15. Change in Pediatric Evaluation of Disability Inventory

    Measure of amount of disability

    Time frame: Measured at day 1 and discharge 4 weeks later

  16. Pediatric Balance Scale

    Measure of balance

    Time frame: Measured at day 1 and discharge 4 weeks later

07

Study locations

1 site
  • University of Missouri Healthcare Children's Therapy Center
    Columbia, Missouri 65211, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04891328
Lead sponsor
University of Missouri-Columbia
Responsible party
Jamie Hall (Assistant Teaching Professor, University of Missouri-Columbia) — Principal investigator
First posted
May 18, 2021
Start date
May 24, 2021
Primary completion
Sep 1, 2021
Completion
Oct 1, 2021
Last update
Mar 28, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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