Effect of Rehabilitation of Patients With a Central Nervous System Lesion

NCT ID: NCT00837460

Last Updated: 2010-03-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-09-30

Study Completion Date

2009-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Stroke

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Intervention Model

CROSSOVER

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

rehabilitation

Bilateral and unilateral prehension oriented rehabilitation to enhance prehension.

Group Type EXPERIMENTAL

rehabilitation

Intervention Type OTHER

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.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

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

Exclusion Criteria

* Diabetuss
* Other Upper Limb pathologies
* MMSE \< 26
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Fondation Saint Luc

UNKNOWN

Sponsor Role collaborator

Fonds pour la recherche scientifique médicale (FRSM), Belgium

UNKNOWN

Sponsor Role collaborator

Association nationale d'aide aux personnes handicapées (ANAH)

UNKNOWN

Sponsor Role collaborator

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Université Catholique de Louvain

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Delphine Dispa, PhD student

Role: PRINCIPAL_INVESTIGATOR

Rehabilitation and physical medecine Unit - UCL

Jean-Louis Thonnard, PhD

Role: STUDY_DIRECTOR

Rehabilitation and physical medecine Unit-UCL

Yannick Bleyenheuft, PhD student

Role: PRINCIPAL_INVESTIGATOR

Rehabilitation and physical medecine Unit-UCL

Thierry Lejeune, MD PhD

Role: STUDY_DIRECTOR

Rehabilitation and physical medecine Unit-UCL

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

READ : Rehabilitation and physical medecine Unit

Brussels, Brussels Capital, Belgium

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Belgium

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2006/06NOV/207

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Multicenter Rehabilitation Study in Acute Stroke
NCT00849303 UNKNOWN PHASE2/PHASE3
Physiotherapy/hypnosis for AVC Patients
NCT06885294 ENROLLING_BY_INVITATION NA