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Clinical Trials/NCT00359255
NCT00359255
Completed
N/A

The Effect of a Supplementary Exercise Program for Upper Extremity Function in Stroke Rehabilitation

University of British Columbia4 sites in 1 country120 target enrollmentJuly 2006
ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
University of British Columbia
Enrollment
120
Locations
4
Primary Endpoint
The primary outcome is the ability to use the paretic arm in activities of daily living. This outcome will be measured pre and post program.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study would focus on a new method of adding extra arm exercise to the usual therapy delivered in the hospital. We propose to design an exercise program for the affected arm and hand that would be given to the client as homework and done in the client's hospital room. The program would be designed and monitored by a therapist that works in the hospital.

We believe that this program will: 1) increase arm and hand recovery over usual care received in the hospital, 2) help people make the move from therapist run exercise to self management of exercise, and 3) promote family involvement in therapy.

Detailed Description

In total 250 participants admitted for stroke rehabilitation at 4 BC sites will be randomly assigned to either the experimental or the control group. The extra arm and hand exercise program (experimental group) will receive usual therapy plus 60 minutes per day of additional arm exercises. This program will last for 4 weeks while the participant is in the hospital. The arm and hand program will include muscle strengthening and stretching, repetitive reaching, folding, stacking, pushing and pulling tasks, picking up objects, and activities that use speed and accuracy. The family will be encouraged to participate in the program with the participant. The control group will receive usual therapy only.

Registry
clinicaltrials.gov
Start Date
July 2006
End Date
December 2008
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Janice Eng

Principal Investigator

University of British Columbia

Eligibility Criteria

Inclusion Criteria

  • 19 years of age or older
  • arm recovery as a rehabilitation goal
  • have palpatable movement of wrist extension
  • able to follow 3 step verabal commands

Exclusion Criteria

  • unstable cardiovascular status (congestive heart failure, uncontrolled hypertension, uncontrolled atrial fibrillation, or left ventricular failure),
  • significant musculo-skeletal problems (e.g., rheumatoid arthritis) or neurological conditions (e.g., Parkinson's disease) due to conditions other than stroke,
  • receptive aphasia

Outcomes

Primary Outcomes

The primary outcome is the ability to use the paretic arm in activities of daily living. This outcome will be measured pre and post program.

Secondary Outcomes

  • Secondary outcomes include amount of use and quality of movement of the paretic arm, motor recovery, strength, tone, and health related quality of life. Each of these measures will be evaluated pre and post program.

Study Sites (4)

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