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Clinical Trials/NCT02066116
NCT02066116
Terminated
Not Applicable

Effect of Kinect-based Upper Limb Rehabilitation System in Patients With Stroke: A Pilot Trial

Seoul National University Bundang Hospital1 site in 1 country23 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Seoul National University Bundang Hospital
Enrollment
23
Locations
1
Primary Endpoint
Change from Baseline in Fugl-Meyer Assessment Scale for upper extremity at 2 weeks
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

The investigators have developed the kinect-based upper extremity rehabilitation program and designed this protocol to prove the efficacy of this program.

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.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
November 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nam-Jong Paik

MD, PhD

Seoul National University Bundang Hospital

Eligibility Criteria

Inclusion Criteria

  • Age from 20 to 80 years
  • Stroke within prior 3 months
  • Unilateral upper extremity weakness

Exclusion Criteria

  • Uncontrolled medical conditions
  • Who cannot obey the simple command
  • Who has the hemispatial neglect, visual impairment, apraxia

Outcomes

Primary Outcomes

Change from Baseline in Fugl-Meyer Assessment Scale for upper extremity at 2 weeks

Time Frame: Baseline, 2 weeks after the baseline

Secondary Outcomes

  • Box and Block Test(Baseline, 2 weeks after the baseline, 6 weeks after the baseline, 14 weeks after the baseline)
  • Modified Barthel Index(Baseline, 2 weeks after the baseline, 6 weeks after the baseline, 14 weeks after the baseline)
  • Brunnstrom stage(Baseline, 2 weeks after the baseline, 6 weeks after the baseline, 14 weeks after the baseline)
  • Number of movement counts during rehabilitation using accelerometer data(Baseline, 2 weeks after the baseline)

Study Sites (1)

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