CompletedNo phase
Motivating Occupational Virtual Experiences In Therapy for Kids
Key facts
- Who runs it
- Barron Associates, Inc.
- Where
- Charlottesville and Durham, United StatesSee the 2 sites
- Trial code
- Status
- Completed
- People taking part
- 25 people enrolled
- Started
- 17 Jun 2022
- Ended
- 15 Jun 2024
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- MOVE-IT Intervention
- UCT Control
- Record updated
- 15 October 2025
Who can take part
- Age
- 4 years to 14 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 15 criteriaShow less
Who can take part
- Diagnosis of hemiplegia resulting from cerebral palsy, stroke, or other form of brain injury
- Medically stable
- Participant has antigravity strength in the affected UE at the elbow to at least 45 degrees of active flexion
- Participant has antigravity shoulder strength in the affected UE to at least 30 degrees each in active flexion, abduction/adduction, and 15 degrees in active internal/external rotation when in an upright and seated position
- Participant has ability to perform a basic color-matching test and identify characters on a vision chart
- Participant must be available to attend study visits during an approximately 3-week participation period
- Willingness and ability to comply with scheduled visits and study procedures
Who cannot take part
- Has received another form of intensive UE therapy, such as CIMT, within the prior 6 months
- History of uncontrolled seizures
- Diagnosis of moderate to severe cortical-visual impairment that in the judgement of the Principal Investigator could adversely impact the subject's participation
- Unwillingness or inability to understand or follow verbal directions
- Psychological diagnosis that in the determination of the Principal Investigator could significantly impact subject's participation or that could be aggravated by study participation
- Determination that participation would result in over exertion, or significant discomfort or pain
- Determination that participation would result in significant agitation or elevated stress
- Visual field deficit in either eye that impairs the ability to view the computer monitor
Where in United States
- University of Virginia (UVA)Charlottesville, United StatesNo longer taking part
- Duke UniversityDurham, United StatesNo longer taking part
About the trial
What the trial wants to find out
A rater-blinded randomized controlled trial (RCT) will be conducted to compare the efficacy of MOVE-IT use in a remotely supervised home exercise program (HEP) to usual care for recovery of upper extremity (UE) function in children with hemiplegia.
The 2 groups in the trial
- MOVE-IT Home Exercise Program (HEP)Treatment being tested
Participants will be asked to employ the MOVE-IT system for upper extremity practice at home 1 hour/day, 5 days/week over a 10-week period.
Treatment: MOVE-IT Intervention
- Usual Care Treatment (UCT) ControlExisting treatment, for comparison
Children in the UCT group will be followed as they continue to receive their previously prescribed therapy services. These children will not receive any treatment services through the study as UCT group participants.
Treatment: UCT Control
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Motivating Occupational Virtual Experiences In Therapy for Kids (MOVE-IT)
- Record updated
- 15 October 2025