ClinicalTrials.gg
Enrolling by invitationNCT04789746Updated Aug 18, 2026

Ready, Set, Go! A Physical Fitness Intervention for Children With Mobility Challenges

An interventional study of adapted Chicago Run running program in Cerebral Palsy, Myelomeningocele and Arthrogryposis, sponsored by Northwestern University. Enrolling by invitation at 1 site in United States. Open to participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Northwestern University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years after the study started (first participant enrolled Feb 2019, registered Mar 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
6 Years to 18 Years
Sex
All
01

Study summary

Barriers to keeping and maintaining fitness as a young person with a disability exist across many domains of access to community locations such as fitness centers, so looking outside of these establishments may be necessary to advance fitness. This study is aimed at piloting a program that would address some of these barriers by hosting a modified after school running program with an underserved population in an accessible way. There is a second option to participate outside of school.

02

Conditions studied

  • Cerebral Palsy
  • Myelomeningocele
  • Arthrogryposis
  • Motor Skills Disorders
  • Gross Motor Development Delay
03

In context

Cerebral Palsy

1,936 studies on the registry are indexed under Cerebral Palsy; 458 are open to participants now.

This study's planned enrollment of 25 is below the median of 34 across 1,431 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

Northwestern University is the lead sponsor of 1,423 studies on the registry; 198 are open to participants now.

Of its 105 completed or terminated interventional studies of FDA-regulated products, 78 (74%) have results posted.

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

04

Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • a medical diagnosis (for example, cerebral palsy) that causes them mobility limitations

Exclusion criteria

Exclusion Criteria:

  • concurrent medical condition that would make exercise unsafe,
  • are unable to follow simple commands
  • have behaviors that would potentially compromise safety of fellow runners or caregivers
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (estimated)

Study arms

  • Experimental
    Running group

    Participants that will join the running program.

    Behavioral: adapted Chicago Run running program

Interventions

  • Behavioraladapted Chicago Run running program

    The intervention being piloted is a 6-8 week running program modified from a running curriculum designed for school-aged children. The children will use a RaceRunner device to facilitate their participation, but this device is not explicitly evaluated in this study. Depending on transportation, they may be given access to the device in their home or school between sessions after it has been fit for them. If given access, guardians will be instructed on care and usage.

06

What researchers measure

Primary outcomes

  1. Goal attainment scale

    a tool designed to standardize the setting and scaling of goals in a way that allows for both improvement and regression as a result of intervention.

    Time frame: at 8 weeks.

  2. 6 min walk test

    Participant will walk as far as they can in 6 minutes, as a measure of endurance

    Time frame: baseline

  3. 6 min walk test

    Participant will walk as far as they can in 6 minutes, as a measure of endurance

    Time frame: at 8 weeks

  4. 30 second walk test

    Participant will walk as fast as they can for 30 seconds, as a measure of speed.

    Time frame: baseline

  5. 30 second walk test

    Participant will walk as fast as they can for 30 seconds, as a measure of speed.

    Time frame: at 8 weeks

  6. Resting heart rate

    Participant heart rate after 5 minutes of quiet sitting

    Time frame: baseline

  7. Resting heart rate

    Participant heart rate after 5 minutes of quiet sitting

    Time frame: at 8 weeks

Secondary outcomes

  1. Surveys

    Participants and their parents will answer questions about baseline level of activity, their perception of themselves, and areas of personal strength

    Time frame: baseline

  2. Surveys

    Participants and their parents will answer questions about baseline level of activity, their perception of themselves, and areas of personal strength

    Time frame: at 8 weeks

  3. Selective Control Assessment of the Lower Extremity (SCALE)

    a method of assessing the ability of a participant to isolate motion to an individual joint of the lower extremity. Min score=0; max score=16, a higher score is a better outcome

    Time frame: baseline

  4. Selective Control Assessment of the Lower Extremity (SCALE)

    a method of assessing the ability of a participant to isolate motion to an individual joint of the lower extremity Min score=0; max score=16, a higher score is a better outcome

    Time frame: at 8 weeks

07

Study locations

1 site
  • Northwestern University
    Chicago Heights, Illinois 60611, United States
08

References and documents

Individual participant data

Plan to share: Undecided

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 Aug 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04789746
Collaborators
Chicago Run, American Academy of Cerebral Palsy and Developmental Medicine
Responsible party
Theresa Moulton (Assistant Professor, Northwestern University) — Principal investigator
First posted
Mar 10, 2021
Start date
Feb 20, 2019
Primary completion
Dec 2027 (estimated)
Completion
Dec 2028 (estimated)
Last update
Aug 18, 2026

Oversight

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

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No contact was published for this record. The registry link below has the sponsor’s details.

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