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Bilateral Training Versus Unilateral Training in Stroke

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University of Illinois

Status and phase

Completed
Phase 2

Conditions

Stroke
Hemiparesis

Treatments

Behavioral: bilateral upper extremity training
Behavioral: Unilateral upper extremity training

Study type

Interventional

Funder types

Other

Identifiers

NCT00681434
2006-0234

Details and patient eligibility

About

This randomized, single-blind study compares the effectiveness of bilateral training to unilateral training for individuals with moderate hemiparesis. We hypothesize that bilateral training will be superior to unilateral in the proximal extremity but not the distal one.

Full description

Upper extremity hemiparesis is the most common post-stroke disability. Longitudinal studies have indicated that 30 to 66 percent of stroke survivors do not have full arm function six months post-stroke. Bilateral arm training has been investigated as a potential rehabilitation intervention for individuals not eligible for constraint induced movement therapy.

This training study included 24 hours of treatment over eight weeks. The protocol consisted of reaching activities with rhythmic auditory cueing emphasizing the proximal arm. Subjects assigned to the bilateral group performed bilateral symmetrical activities while subjects in the unilateral group performed the same activity with the affected arm only. The Motor Assessment Scale-Upper Limb Item and the Motor Status Scale are used as primary outcome measures. The Reaching Performance Scale and strength measures are secondary outcome measures. Assessments are administered pre-/ and post-training by a blind rater.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • cortical or subcortical stroke
  • chronic condition (at least six months prior)
  • ability to follow 2-step commands
  • ability to give consent

Exclusion criteria

  • lesion in brain stem or cerebellum
  • visual field cut
  • neglect
  • uncontrolled hypertension
  • angina
  • COPD

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

1
Experimental group
Description:
bilateral training
Treatment:
Behavioral: bilateral upper extremity training
2
Active Comparator group
Description:
Unilateral training
Treatment:
Behavioral: Unilateral upper extremity training

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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