Skip to main content
Clinical Trials/NCT02995213
NCT02995213
Completed
N/A

Quantification of UE Use and Effects of Feedback in the Home Setting

Cleveland State University0 sites12 target enrollmentNovember 2015
ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Cleveland State University
Enrollment
12
Primary Endpoint
Accelerometer based paretic arm amount of use
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The investigators are proposing a pilot study, the purpose of which is to use accelerometers to quantify UE use (1 and two hand use) in people post-stroke from which the investigators will develop use-based feedback to improve recovery in the home setting. The objectives of this pilot study are to:

i.) determine the feasibility of using accelerometers to quantify amount of UE use in the home setting in individuals chronic post-stroke,

ii.) quantify and compare the unilateral activity of the weaker (paretic) versus stronger (non-paretic) UEs, and

iii.) assess the effect of a 7 sessions of in-home accelerometer used-based feedback on unilateral and bilateral UE use.

iv.) assess kinematic, kinetic, and EMG data during UE movements unilaterally and bilaterally in subjects post-chronic stroke pre and post feedback.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
December 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maureen Whitford

Assistant Professor

Cleveland State University

Eligibility Criteria

Inclusion Criteria

  • Subjects post-stroke
  • chronic post ischemic or hemorrhagic cortical or subcortical stroke
  • 25 - 100 years old
  • upper extremity impairment
  • Subjects will need to be able to flex their paretic shoulder and their elbow \> 40° without assist
  • able to follow 2-step commands
  • community dwelling with or without assistance
  • intact superficial light touch sensation in both upper extremities
  • must also have some movement in both arms

Exclusion Criteria

  • can't currently have another neuromuscular disorders such as spinal cord injury, traumatic brain injury, Parkinson disease or multiple sclerosis
  • no upper extremity injury within the last 3 months

Outcomes

Primary Outcomes

Accelerometer based paretic arm amount of use

Time Frame: 3 week period

Similar Trials