Feasibility, safety, and efficacy of pediatric constraint-induced movement therapy for patients with upper extremity hemiparesis
Not Applicable
Recruiting
- Conditions
- Patients with upper extremity hemiparesis due to cerebral palsy, stroke, brain tumor and traumatic brain injury.
- Registration Number
- JPRN-UMIN000039715
- Lead Sponsor
- Hyogo college of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 22
Inclusion Criteria
Not provided
Exclusion Criteria
1) Unable to understand simple order 2) Uncontrolled complications 3) Unable to obtain informed consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Outcome Measures 1) The feasibility of research protocol 2) Adverse events 3) Jebsen Taylor Test of Hand Function Test Assessment timing Outcome measures were assessed at baseline, after intervention, 1 month follow up, 6 months follow up and 12 months follow up. Statistical assessment Short-term effect: t test or Wilcoxon signed rank test Long-term effect: ANOVA or Kruskal-Wallis or Dunnet Tukey-Kramer,or Bonferroni method
- Secondary Outcome Measures
Name Time Method (1) Fugl-Meyer Assessment (2) Pediatric Motor Activity Log-Revised Assessment timing Outcome measures were assessed at baseline, after intervention, 1 month follow up, 6 months follow up and 12 months follow up. Statistical assessment Short-term effect: t test or Wilcoxon signed rank test Long-term effect: ANOVA or Kruskal-Wallis or Dunnet Tukey-Kramer,or Bonferroni method