Children With Hemiparesis Arm and Hand Movement Project (CHAMP Study) (CHAMP)
Primary Purpose
Hemiparesis, Cerebral Palsy, Brain Injury
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Variations in Pediatric Constraint-Induced Movement Therapy (P-CIMT) versus usual and customary rehabilitation
Sponsored by
About this trial
This is an interventional treatment trial for Hemiparesis focused on measuring P-CIMT, Pediatric Constraint Induced Movement Therapy, Hemiparesis, Cerebral Palsy, Children
Eligibility Criteria
Inclusion Criteria:
- are 2 years - 8 years old
- do not have any serious complicating conditions or acute medical concerns
- are diagnosed with cerebral palsy with hemiparesis (prior to age 2)
- have not had botox injections in the last 6 months and
- have not received Constraint-Induced Movement Therapy in the last 6 months
- have a clinical MRI that can be provided in digital format for research project
Exclusion Criteria:
-
Sites / Locations
- Fralin Biomedical Research Institute at Virginia Tech
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Experimental
Experimental
Experimental
Experimental
Active Comparator
Arm Label
Group with continuous constraint and daily therapy
Group with continuous constrainit and 3 days a week therapy
Group with part-time constraint and daily therapy
Group with part-time constraint and 3 days a week therapy
Usual and customary treatment group
Arm Description
Outcomes
Primary Outcome Measures
Functional measurements of change across time in the child's abilities with their arms and hands will be measured using the Assisting Hand Assessment, the Peabody Developmental Motor Scales, and the Pediatric Evaluation and Disability Inventory.
Functional measurements of arm use
Secondary Outcome Measures
Modified version of Quality of Upper Extremity Skills Test (QUEST)
Functional range of motion measure
Full Information
NCT ID
NCT01895660
First Posted
June 25, 2013
Last Updated
March 10, 2022
Sponsor
Virginia Polytechnic Institute and State University
Collaborators
Ohio State University, University of Virginia
1. Study Identification
Unique Protocol Identification Number
NCT01895660
Brief Title
Children With Hemiparesis Arm and Hand Movement Project (CHAMP Study)
Acronym
CHAMP
Official Title
A Multisite Trial of Pediatric Constraint-Induced Movement Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Virginia Polytechnic Institute and State University
Collaborators
Ohio State University, University of Virginia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
What is the CHAMP Study?
The CHAMP Study is a multisite clinical trial funded by the National Institutes of Health that is comparing the efficacy of alternative therapies for young children with unilateral spastic cerebral palsy (or hemiparetic cerebral palsy). Children who meet study eligibility criteria at one of the three clinical sites (Roanoke, VA; Charlottesville, VA, and Columbus, OH) will be invited to enroll, and their parents will be provided all necessary paperwork along with informed consent documentation. Assignment to one of the alternative therapy conditions will be random. Participation in the study includes assessment of each child prior to treatment, close monitoring of the child's progress during treatment, and post-treatment evaluation at the end of therapy, as well as, 6 and 12 months later. Parents will have an active role in the project, both observing their child during therapy sessions and then engaging in home-based activities that allow the child to practice and extend new motor skills. There will be no charge for the therapy provided.
What are the therapies being tested? In the past decade or so, a new form of therapy for children with hemiparetic cerebral palsy was developed and has shown to produce positive changes in individual children and in small clinical trials (e.g., DeLuca, Echols, Ramey, & Taub, 2003; DeLuca, Echols, Law, & Ramey, 2006; Case-Smith, DeLuca, Stevenson, & Ramey, 2012). The therapy is named Constraint-Induced Movement Therapy (CIMT) and refers to a multi-component form of therapy in which the child has the unimpaired or less impaired upper extremity constrained (by a cast or a splint) while also receiving active therapy from a specially trained therapist who shapes new skills and functional activities with the child's more impaired upper extremity. Traditionally, CIMT therapy dosages have been high - often lasting many hours per day, 5 days a week, for 4 consecutive weeks. There are important clinical and scientific questions that need to be answered about the effects of different dosage levels and about different types of constraint on the child's more functional (less impaired) arm and hand. This study will be the first that will directly compare different amounts of therapy and different types of constraint to evaluate what "works best" for young children. The therapy is very play-like and engaging for children, and no negative effects of casting or the high dosages have been detected in previous clinical trials.
Who is eligible: Children between 2 and 8 years of age with a diagnosis of unilateral spastic cerebral palsy or hemiparetic cerebral palsy. Children must be relatively healthy, not currently receiving Botox (or other similar medications), and able to understand simple communication and instructions. In advance, the treatment will be explained in detail to parents and a written protocol available to share with the child's physician and other current therapist for review. During the one month of treatment, children will not receive other forms of physical or occupational therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemiparesis, Cerebral Palsy, Brain Injury
Keywords
P-CIMT, Pediatric Constraint Induced Movement Therapy, Hemiparesis, Cerebral Palsy, Children
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
124 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group with continuous constraint and daily therapy
Arm Type
Experimental
Arm Title
Group with continuous constrainit and 3 days a week therapy
Arm Type
Experimental
Arm Title
Group with part-time constraint and daily therapy
Arm Type
Experimental
Arm Title
Group with part-time constraint and 3 days a week therapy
Arm Type
Experimental
Arm Title
Usual and customary treatment group
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Variations in Pediatric Constraint-Induced Movement Therapy (P-CIMT) versus usual and customary rehabilitation
Intervention Description
Types of constraint and dosage amounts will be varied.
Primary Outcome Measure Information:
Title
Functional measurements of change across time in the child's abilities with their arms and hands will be measured using the Assisting Hand Assessment, the Peabody Developmental Motor Scales, and the Pediatric Evaluation and Disability Inventory.
Description
Functional measurements of arm use
Time Frame
Pretreatment; Post-Treatment, 6 and 12 months Follow up
Secondary Outcome Measure Information:
Title
Modified version of Quality of Upper Extremity Skills Test (QUEST)
Description
Functional range of motion measure
Time Frame
Pre treatment; Post-Treatment (end of 4 weeks of treatment), 6 and 12 months Follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
are 2 years - 8 years old
do not have any serious complicating conditions or acute medical concerns
are diagnosed with cerebral palsy with hemiparesis (prior to age 2)
have not had botox injections in the last 6 months and
have not received Constraint-Induced Movement Therapy in the last 6 months
have a clinical MRI that can be provided in digital format for research project
Exclusion Criteria:
-
Facility Information:
Facility Name
Fralin Biomedical Research Institute at Virginia Tech
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24016
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
34649982
Citation
Ramey SL, DeLuca SC, Stevenson RD, Conaway M, Darragh AR, Lo W; CHAMP. Constraint-Induced Movement Therapy for Cerebral Palsy: A Randomized Trial. Pediatrics. 2021 Nov;148(5):e2020033878. doi: 10.1542/peds.2020-033878. Epub 2021 Oct 14.
Results Reference
derived
PubMed Identifier
30782701
Citation
Ramey SL, DeLuca S, Stevenson RD, Case-Smith J, Darragh A, Conaway M. Children with Hemiparesis Arm and Movement Project (CHAMP): protocol for a multisite comparative efficacy trial of paediatric constraint-induced movement therapy (CIMT) testing effects of dosage and type of constraint for children with hemiparetic cerebral palsy. BMJ Open. 2019 Jan 15;9(1):e023285. doi: 10.1136/bmjopen-2018-023285.
Results Reference
derived
Links:
URL
https://publications.aap.org/pediatrics/article/148/5/e2020033878/181349/Constraint-Induced-Movement-Therapy-for-Cerebral
Description
Constraint-Induced Movement Therapy for Cerebral Palsy: A Randomized Trial
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Children With Hemiparesis Arm and Hand Movement Project (CHAMP Study)
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