Arm More + Camp: An Implementation Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Modified Constraint Induced Movement Therapy.
- Who it may be relevant to
- Registry conditions: Hemiplegia, Cerebral Palsy Spastic Hemiplegic, Acquired Brain Injury (Including Stroke). Basic parameters: 5 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Arm More + Camp: An Implementation Study of a Modified Constraint Induced Movement Therapy Camp for Children With Hemiparesis
Overview
Our primary aim is to evaluate the implementation cost of a full day modified constraint induced movement therapy camp for children with hemiparesis. Participants will complete a day camp (9am to 4pm) with constraint induced movement therapy in Week 1 and bimanual therapy in Week 2.
Interventions
- Behavioral Modified Constraint Induced Movement Therapy
Constraint Induced Movement Therapy and Bimanual Therapy
Primary outcome measures
- Implementation Cost [Time frame: From enrolment to the end of outcome data collection at 3 weeks]
Secondary outcome measures (1)
- Canadian Occupational Performance Measure [Time frame: Baseline and the end of treatment at 2 weeks]
Eligibility criteria
Inclusion criteria
- Mild to moderate hemiparesis due to cerebral palsy or acquired brain injury (e.g, traumatic brain injury, stroke)
- Ability to actively extend wrist to neutral and actively flex and extend fingers (at minimum)
- Attend school full-time
- Able to participate in group activities
- Written consent
Exclusion criteria
- Severe hemiparesis due to cerebral palsy or acquired brain injury
- No wrist movement on the hemiplegic hand.
- Unable to concentrate for periods of 60-90minutes
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
Canada · 1 center
- Alberta Children's Hospital — Calgary
Identifiers
NCT: NCT07065916 · REB25-0524