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Clinical Trials/NCT03867838
NCT03867838
Completed
N/A

Effects of Post-Stroke Upper Extremity Assistance

Stanford University1 site in 1 country6 target enrollmentJune 14, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Arm Weakness as a Consequence of Stroke
Sponsor
Stanford University
Enrollment
6
Locations
1
Primary Endpoint
Percent Change From Baseline in Reachable Workspace
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to show that a wearable compliant arm support consisting of inflatable bladders with adjustable straps to connect them to the waist and arm can meaningfully increase the reachable workspace of persons with post-stroke arm weakness.

Registry
clinicaltrials.gov
Start Date
June 14, 2019
End Date
October 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Allison Okamura

Professor of Mechanical Engineering

Stanford University

Eligibility Criteria

Inclusion Criteria

  • greater than 6 months post-stroke
  • passive abduction to 90 degrees at shoulder
  • reduced active (retro)flexion/extension at shoulder when abducted to 90 degrees
  • reduced active flexion/extension at elbow

Exclusion Criteria

  • unable to give informed consent
  • unable to comprehend and follow instructions
  • have a condition (other than stroke) affecting sensorimotor function
  • show evidence of unilateral spatial neglect
  • unable to sit in a chair without armrests for 2 hours

Outcomes

Primary Outcomes

Percent Change From Baseline in Reachable Workspace

Time Frame: baseline, while using support device, and 30 minutes following removal of support device (up to 4 minutes per assessment)

Reachable workspace was measured using a PhaseSpace motion capture system, recorded as an area (in square meters).

Secondary Outcomes

  • Percent Change From Baseline in Biceps Activation(baseline and while using support device (up to 10 seconds per assessment))

Study Sites (1)

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