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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00740402
Other study ID # GPalma
Secondary ID GPalma 123
Status Completed
Phase N/A
First received August 22, 2008
Last updated April 15, 2010
Start date January 2008
Est. completion date January 2009

Study information

Verified date August 2008
Source Faculdades Metropolitanas Unidas
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate the process of acquiring a motor skill subject in post-stroke, comparing them with healthy subjects.


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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date January 2009
Est. primary completion date July 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 45 Years to 65 Years
Eligibility 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 Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil University Center of Metropolitan United São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Faculdades Metropolitanas Unidas

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary TIME time (in seconds) 3 times in a week (acquisition, transfer an retention phase) Yes
Secondary error number of mistakes made by the subjects 3 times in a week (acquisition, transfer an retention phase) Yes
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