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Clinical Trials/NCT00837460
NCT00837460CompletedNot Applicable

Effect of Rehabilitation of Patients With a Central Nervous System Lesion

Cliniques universitaires Saint-Luc- Université Catholique de Louvain2 sites in 1 country15 target enrollmentStarted: September 1, 2006Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
15
Locations
2
Primary Endpoint
prehension functionality
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The purpose of the study is to analyse the prehensions deficits and the effect of prehension rehabilitation in central nervous system lesioned people

Study Design

Study Type
Interventional
Intervention Model
Crossover
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
16 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Adult minimum 6mounth after first stroke
  • •Minimal prehension of both hands

Exclusion Criteria

  • •Diabetuss
  • •Other Upper Limb pathologies
  • •MMSE < 26

Outcomes

Primary Outcomes

prehension functionality

Time Frame: 4 weeks before, just before, after first part and after the second part of rehabilitation

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Sponsor Class
Other

Study Sites (2)

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