Robot-Assisted Hand Motor Therapy for Subjects With Hemiparetic Stroke

University of California, Irvine41 enrolled

Overview

The purpose of this study is to develop and assess the effectiveness of robot-assisted movement therapy in enhancing hand motor function in subjects with chronic hemiparetic stroke, and to identify predictors of treatment response.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Stroke

Interventions

Hand & Wrist Assisting Robotic DeviceDEVICE

Treatment occurs in 2 hour sessions, 4 times a week over 3 weeks. In each treatment session, you will sit in a chair and have your weak hand attached to a mechanical device (the robot), which will help you open and close your hand. During the treatment, different types of objects (with varying shapes, sizes, and weight) will be placed into your hand. You will be given a variety of instructions related to the grasping, feeling, or identifying of the object in your hand. Sometimes these instructions will be given from the investigator and sometimes from the computer. You will often be asked to grasp, or release, each of these objects as best you can. You will also be asked to concentrate on the object in your hand. An example of what you may be asked to do is to name the object. During other times, you will play games, using the robot to control game parts on the computer screen. At other times, you will move your hand so that the robot can measure your hand function.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. At least 18 years old 2. Had stroke between 11-26 weeks ago 3. Have some weakness in one of your wrists or hands due to stroke 4. Did not have too much disability prior to stroke 5. Do not have major depression Exclusion Criteria: 1. Non-English speaking 2. If you have trouble keeping good attention 3. Pregnant, advanced liver, kidney, heart, or lung disease 4. Terminal medical diagnosis or major neurological or psychiatric disease apart from stroke 5. Cannot undergo MRI scanning 6. Have history of brain surgery or seizures

Locations (1)

University of California, Irvine

Irvine, California, United States

Outcomes

Primary Outcomes

Action Research Arm Test

The Action Research Arm Test is a 19 item measure divided into 4 sub-tests (grasp, grip, pinch, and gross arm movement). Performance on each item is rated on a 4-point ordinal scale ranging from: 3: Performs test normally 2: Completes test, but takes abnormally long or has great difficulty 1: Performs test partially 0: Can perform no part of test. The test is used to determine upper limb function, 0-57 points with higher is better, 57 is the highest score indicating normal arm movement.

Time frame: change from baseline to 1 month post-end treatment, Intention To Treat

Arm Motor Fugl-Meyer Test

The Arm Motor Fugl-Meyer test is an assessment of Sensorimotor Recovery After Stroke. It is a 33 item measure with 3 subgroups which are Proximal, Wrist/Hand, and Coordination/Speed. The scaling for each item works on a scale of 0-2 with 0 being not able to be done, 1 being partially done, and 2 being done normally. The scoring goes from 0-66, higher is better, 66 is considered a normal score with no noticable complications in movement.

Time frame: change from baseline to 1 month post-end treatment, Intention To Treat

Data from ClinicalTrials.gov

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