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Clinical Trials/NCT02890446
NCT02890446
Completed
Not Applicable

A Randomized Control Trial on the Effects of Attentional Focus on Motor Training of the Upper Extremity Using Robotics With Individuals After Chronic Stroke

New York Presbyterian Hospital0 sites33 target enrollmentMay 2014
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
New York Presbyterian Hospital
Enrollment
33
Primary Endpoint
Change in quality of arm motion measured by smoothness at the start of arm training, at 4week, and 8 weeks.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study compares the effects of an internal versus an external focus of attention on motor training of the affected arm for individuals with stroke. Participants were randomly assigned to either the internal or external focus treatment groups and received 12 sessions of arm training.

Detailed Description

Participants were randomized to one of two treatment groups and received upper arm reaching training on the InMotion 2 shoulder robot (12 hourly sessions over four weeks). The external focus group received instructions specifically to pay attention to the task goal--hitting targets on the video game, while the internal focus group was instructed to pay attention to the movement of their arm motions (video game monitor was turned off). Both groups practiced the same arm reaching pattern and were matched for level of arm impairment and training dosage.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
November 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Grace Kim

Assistant Professor

New York Presbyterian Hospital

Eligibility Criteria

Inclusion Criteria

  • diagnosis of stroke \> 6 months
  • moderate to severe arm impairment
  • intact visual scanning and spatial orientation of the affected arm
  • functional cognitive status
  • medically stable

Exclusion Criteria

  • concurrent occupational or physical therapy for the arm
  • joint contractures at the wrist, forearm, elbow, or shoulder
  • moderate to severe spasticity at the elbow or shoulder
  • presence of other neurological conditions
  • botulinum toxin injection in the affected arm \< 3 months prior
  • score of 0/5 on manual muscle test at the elbow or shoulder

Outcomes

Primary Outcomes

Change in quality of arm motion measured by smoothness at the start of arm training, at 4week, and 8 weeks.

Time Frame: baseline, 4 weeks, 8 weeks

kinematic assessment of arm motion measured by average velocity decided by maximum velocity

Change in coordination at the shoulder and elbow measured by joint independence after arm training assessed start of training, discharge and at follow up.

Time Frame: baseline, 4 weeks, 8 weeks

kinematic measure of coordination between the shoulder and elbow joint

Change in motor impairment of the arm measured by Fugl-Meyer Assessment (FMA) at the start of training, discharge, and follow up.

Time Frame: baseline, 4 weeks, 8 weeks

performance based assessment of underlying motor impairment of the affected shoulder, elbow, hand after stroke

Change in motor impairment and functional ability of the arm measured by the Wolf Motor Function Test (WMFT) at start of training, discharge, and follow up.

Time Frame: baseline, 4 weeks, 8 weeks

performance based assessment of underlying motor impairment and function of the affected arm after stroke

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