Kinect-based Upper Limb Rehabilitation System in Stroke Patients
NCT ID: NCT02066116
Last Updated: 2017-11-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
23 participants
INTERVENTIONAL
2014-11-30
2017-11-30
Brief Summary
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In brief, subacute stroke patients allocated to intervention group will receive the kinect based-rehabilitation program plus conventional occupational therapy and patients allocated to control group will receive the sham virtual rehabilitation plus conventional occupational therapy, for 10 days.
20 patients with subacute stroke will be allocated into each group and after completing the 10 days intervention, they will be assessed by using objective assessment tools for upper extremity function.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Kinect-based Rehabilitation
Kinect-based rehabilitation plus occupational therapy
The developed kinect-based rehabilitation system will be used for 30min/session. Conventional 30min occupational therapy also will be applied for the patient enrolled.
Self-exercises education
sham virtual rehabilitation education plus occupational therapy
For the sham virtual rehabilitation, computer-based cognitive rehabilitation program will be used. Patients will be encouraged to use their affected arm to push the button but the motion will be minimal and not related to the concept of upper extremity rehabilitation.
Interventions
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Kinect-based rehabilitation plus occupational therapy
The developed kinect-based rehabilitation system will be used for 30min/session. Conventional 30min occupational therapy also will be applied for the patient enrolled.
sham virtual rehabilitation education plus occupational therapy
For the sham virtual rehabilitation, computer-based cognitive rehabilitation program will be used. Patients will be encouraged to use their affected arm to push the button but the motion will be minimal and not related to the concept of upper extremity rehabilitation.
Eligibility Criteria
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Inclusion Criteria
* Stroke within prior 3 months
* Unilateral upper extremity weakness
Exclusion Criteria
* Who cannot obey the simple command
* Who has the hemispatial neglect, visual impairment, apraxia
20 Years
80 Years
ALL
No
Sponsors
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Microsoft Research
INDUSTRY
Ministry of Science and ICT, Republic of Korea
OTHER_GOV
Seoul National University Bundang Hospital
OTHER
Responsible Party
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Nam-Jong Paik
MD, PhD
Principal Investigators
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Nam-Jong Paik, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea
Locations
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Seoul National University Hospital
Seongnam-si, Gyeonggi-do, South Korea
Countries
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Related Links
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Related Info
Related Info
Other Identifiers
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B1401-234-001
Identifier Type: -
Identifier Source: org_study_id