Perfetti Method in Upper Extremity of Stroke Patients
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01374152|
Recruitment Status : Completed
First Posted : June 15, 2011
Last Update Posted : July 17, 2012
|Condition or disease||Intervention/treatment||Phase|
|Stroke||Other: cognitive sensory motor training therapy||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||A Randomized Controlled Trial of Cognitive Sensory Motor Training Therapy on the Recovery of Upper Extremity Function in Acute Stroke Patients|
|Study Start Date :||July 2008|
|Primary Completion Date :||May 2011|
|Study Completion Date :||June 2011|
Cognitive sensory motor training method for upper extremities rehabilitation every working day, totally training not less than 600 minutes within 4 weeks.
Other: cognitive sensory motor training therapy
training method that emphasis on cognition/ sensation/ and motor movement together train every working day 45 minutes per day for 4 weeks.
No Intervention: conventional rehabilitation
conventional occupational therapy method for upper extremities rehabilitation every working day, totally training not less than 600 minutes within 4 weeks.
- Action research arm test [ Time Frame: 4 weeks ]The Action research arm test used for assess the impairment of upper limb function. ARAT has ordinal 4-point scale (0-3) in 19 items. Totally 57 scores.
- Box and block test [ Time Frame: 4 weeks. ]For evaluated gross manual dexterity, consist of two adjacent boxes of the same size. Between the two boxes, there is a partition. It is recorded the number of wooden block that can be transported from one compartment of a box to another within 60 seconds
- Extended Barthel Index [ Time Frame: 4 weeks. ]Basic activity of daily living and degree of independence from any form of help.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01374152
|Prasat neurological institute|
|Bangkok, Thailand, 10400|
|Principal Investigator:||Ratanapat Chanubol, MD.||Prasat Neurological Institute|