- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00740402
Motor Learning of a Planning Task in Stroke Patients: the Maze Paradigm Measured Through Time and Error as Variables
April 15, 2010 updated by: Faculdades Metropolitanas Unidas
Motor Learning of a Planning Task in Stroke Patients
The purpose of this study is to investigate the process of acquiring a motor skill subject in post-stroke, comparing them with healthy subjects.
Study Overview
Status
Completed
Conditions
Detailed Description
20 post-stroke patients were comprised to the experimental group (EG) and 20 health subjects were included to the control group (CG.
Inclusion criteria: chronic stroke, single stroke event, lesion in anterior circulation, right handed subjects, MEEM over 23 points.
The task consisted in a maze paradigm, made by pencil and paper, with the non affected side for EG and left upper extremity for CG.
The instruction was given to the subjects to complete the task as fast as possible.
The study consisted in three phases: acquisition (AQ)with 30 trials, transfer (TR, short retention (R1)and long term retention (R2 both with 5 trials.
Study Type
Observational
Enrollment (Actual)
20
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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São Paulo, Brazil
- University Center of Metropolitan United
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
45 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients after stroke
Description
Inclusion Criteria:
- Age between 40 and 65
- Injury in territory of movement earlier, as shown by examination of image and finding medical neurologist
- Time of injury over 6 months
- Single vascular event
- Right handed, by applying the Inventory of Dominance Side of Edinburgh Mini mental with scores over 23 points
Exclusion Criteria:
- Aphasia of understanding
- Instability clinic
- Other neurological diseases associated (Parkinson's disease, dementias, Alzheimer)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
TIME
Time Frame: 3 times in a week (acquisition, transfer an retention phase)
|
time (in seconds)
|
3 times in a week (acquisition, transfer an retention phase)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
error
Time Frame: 3 times in a week (acquisition, transfer an retention phase)
|
number of mistakes made by the subjects
|
3 times in a week (acquisition, transfer an retention phase)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Camila Torriani, doctor, University of Sao Paulo
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2008
Primary Completion (Actual)
July 1, 2008
Study Completion (Actual)
January 1, 2009
Study Registration Dates
First Submitted
August 22, 2008
First Submitted That Met QC Criteria
August 22, 2008
First Posted (Estimate)
August 25, 2008
Study Record Updates
Last Update Posted (Estimate)
April 16, 2010
Last Update Submitted That Met QC Criteria
April 15, 2010
Last Verified
August 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GPalma
- GPalma 123 (Other Identifier: UNICID/USP)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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