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Clinical Trials/NCT00473447
NCT00473447
Completed
Phase 1

Phase1 Effectiveness of a Modified Constraint-Induced Movement Therapy Program in Rehabilitation of Arm Paresis in Children With Cerebral Palsy: a Cross-Over Study

Universita di Verona0 sites10 target enrollmentJanuary 2004

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Hemiparesis
Sponsor
Universita di Verona
Enrollment
10
Primary Endpoint
Arm Use Test
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to determine if a modified protocol of constraint-induced movement therapy (CIT) is effective in rehabilitation treatment of arm paresis in children with cerebral palsy. In these children one main problem the non-use of the affected arm. Many studies showed that the non-use phenomenon can by reversed by the CIT, a rehabilitation program consisting of 15 days of restraining the unaffected arm plus a daily intensive (6 hours/day) physiotherapy training of the paretic arm. The present study aims at evaluating if a shortened CIT protocol (restraining device plus only 2 weekly hours of physiotherapy) is effective in improving use and function of children paretic arm

Registry
clinicaltrials.gov
Start Date
January 2004
End Date
April 2006
Last Updated
18 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Universita di Verona

Eligibility Criteria

Inclusion Criteria

  • presence of mild-moderate arm paresis (after cerebral palsy) enabling to
  • reach and grasp a pellet
  • age between 1-10 years
  • active participation during proposed activities
  • parents consent for participation -

Exclusion Criteria

  • presence of severe behaviour disturbances
  • presence of severe mental retardation (QI\<60)

Outcomes

Primary Outcomes

Arm Use Test

Time Frame: Four months for each patient

Secondary Outcomes

  • Arm Function Test(Four months for each patient)

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