Effect of Rehabilitation of Patients With a Central Nervous System Lesion

Tracking Information
First Submitted Date ICMJE	February 4, 2009
First Posted Date ICMJE	February 5, 2009
Last Update Posted Date	March 30, 2010
Study Start Date ICMJE	September 2006
Actual Primary Completion Date	September 2009 (Final data collection date for primary outcome measure)
Current Primary Outcome Measures ICMJE; (submitted: February 4, 2009)	prehension functionality [ Time Frame: 4 weeks before, just before, after first part and after the second part of rehabilitation ]
Original Primary Outcome Measures ICMJE	Same as current
Change History	Complete list of historical versions of study NCT00837460 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ICMJE	Not Provided
Original Secondary Outcome Measures ICMJE	Not Provided
Current Other Outcome Measures ICMJE	Not Provided
Original Other Outcome Measures ICMJE	Not Provided
Descriptive Information
Brief Title ICMJE	Effect of Rehabilitation of Patients With a Central Nervous System Lesion
Official Title ICMJE	Not Provided
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
Detailed Description	Not Provided
Study Type ICMJE	Interventional
Study Phase	Not Applicable
Study Design ICMJE	Intervention Model: Crossover Assignment; Masking: Single (Outcomes Assessor); Primary Purpose: Supportive Care
Condition ICMJE	Stroke
Intervention ICMJE	Other: rehabilitation; 4 weeks of bilateral followed or preceded by 4 weeks of unilateral similar prehension oriented repeated rehabilitation tasks. About 45 minutes 3 times a week, the subject is coached by a physiotherapist to enhance his prehension habilities.
Study Arms	Experimental: rehabilitation; Bilateral and unilateral prehension oriented rehabilitation to enhance prehension.; Intervention: Other: rehabilitation
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
Recruitment Information
Recruitment Status ICMJE	Completed
Estimated Enrollment ICMJE; (submitted: February 4, 2009)	15
Original Estimated Enrollment ICMJE	Same as current
Actual Study Completion Date	October 2009
Actual Primary Completion Date	September 2009 (Final data collection date for primary outcome measure)
Eligibility Criteria ICMJE	Inclusion Criteria: Adult minimum 6mounth after first stroke; Minimal prehension of both hands Exclusion Criteria: Diabetuss; Other Upper Limb pathologies; MMSE < 26
Sex/Gender	Sexes Eligible for Study: All
Ages	16 Years and older (Child, Adult, Senior)
Accepts Healthy Volunteers	Yes
Contacts ICMJE	Contact information is only displayed when the study is recruiting subjects
Listed Location Countries ICMJE	Belgium
Removed Location Countries
Administrative Information
NCT Number ICMJE	NCT00837460
Other Study ID Numbers ICMJE	2006/06NOV/207
Has Data Monitoring Committee	Yes
U.S. FDA-regulated Product	Not Provided
IPD Sharing Statement	Not Provided
Responsible Party	Cliniques Universitaires Saint-Luc, Université Catholique de Louvain
Study Sponsor ICMJE	Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Collaborators ICMJE	Fondation Saint Luc; Fonds de la recherche scientifique et médicale (FRSM); Association nationale d'aide aux personnes handicapées (ANAH)
Investigators ICMJE	Principal Investigator: Delphine Dispa, PhD student Rehabilitation and physical medecine Unit - UCL Study Director: Jean-Louis Thonnard, PhD Rehabilitation and physical medecine Unit-UCL Principal Investigator: Yannick Bleyenheuft, PhD student Rehabilitation and physical medecine Unit-UCL Study Director: Thierry Lejeune, MD PhD Rehabilitation and physical medecine Unit-UCL
PRS Account	Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Verification Date	March 2010
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP