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N/A N=40 Randomized Single-blind Treatment

Influence of Timing on Motor Learning

Cerebrovascular Accident

Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: Motor and Strength Outcome Measure Using Box and Block Test — 2.3; 4.3 blocks

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Conventional hand exercise (Other); MusicGlove (Device); Conventional Arm Exercise (Other); Resonating Arm Exerciser (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of California, Irvine
Primary completion
Dec 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Motor and Strength Outcome Measure Using Box and Block Test
2.3; 4.3
PRIMARY
Motor and Strength Outcome Measure Using Fugl-Meyer Score
2.88; 1.31

Summary

The purpose of this research study is to compare different methods for training hand movement at home after stroke. This study involves research because it will test two experimental devices, the MusicGlove and the Resonating Arm Exerciser (RAE), compared to conventional hand and arm exercises. The MusicGlove is a glove that measures finger movements and allows its user to play a musical computer game using those movements. The RAE is a lever that attaches to a manual wheelchair with elastic bands and can be pushed back and forth to exercise the arm.

Eligibility Criteria

Inclusion Criteria

  • Age 18 to 80 years of age
  • Sustained a single stroke affecting the arm, at least three months prior to enrollment
  • Minimal to moderate lost motor control of the arm after stroke
  • No active major psychiatric problems, or neurological/orthopedic problems affecting the stroke-affected upper extremity
  • No active major neurological disease other than the stroke
  • Absence of pain in the stroke-affected upper extremity

Exclusion Criteria

  • Severe tone at the affected upper extremity
  • Severe aphasia
  • Severe reduced level of consciousness
  • Severe sensory/proprioception deficit at the affected upper extremity
  • Currently pregnant
  • Difficulty in understanding or complying with instructions
  • Inability to perform the experimental task that will be studied
  • Increased pain with movement of the stroke-affected upper extremity
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01769326). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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