RECRUITING

Wearable Device and Behavioral Support for Enhancing Arm Use After Stroke

Description

The goal of this study is to determine the effectiveness of behavioral support and feedback from a wearable device that senses arm movement in improving upper extremity function in a pilot, randomized controlled trial with chronic stroke patients

Study Overview

Study Details

Study overview

The goal of this study is to determine the effectiveness of behavioral support and feedback from a wearable device that senses arm movement in improving upper extremity function in a pilot, randomized controlled trial with chronic stroke patients

Sensor Enhanced Activity Motivation After Stroke

Wearable Device and Behavioral Support for Enhancing Arm Use After Stroke

Condition
Chronic Stroke Patients
Intervention / Treatment

-

Contacts and Locations

Irvine

University of California Irvine, Irvine, California, United States, 92697

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 18 to 85 years of age
  • * Experienced a single or multiple, ischemic or hemorrhagic stroke, with unilateral weakness, over six months previously
  • * An ability to score at least 3 blocks on the Box and Block Test. BBT score of the affected arm is at least 5% worse than that present with the unaffected arm.
  • * Absence of major depression, as defined by DSM V criteria or a score on the Geriatric Depression Scale \< 10.
  • * Any substantial decrease in alertness, language reception, or attention
  • * Single or multiple, ischemic or hemorrhagic stroke less than 6 months ago
  • * Severe muscle tone at the upper extremity (score ≥ 3 on the Modified Ashworth Spasticity scale)
  • * Pregnant or lactating
  • * Advanced liver, kidney, cardiac, or pulmonary disease
  • * Coexistent major neurological disease
  • * Coexistent major psychiatric disease
  • * Plans to alter any current participation in other rehabilitation therapy in the time period of the study
  • * A terminal medical diagnosis consistent with survival \< 1 year
  • * A history of significant alcohol or drug abuse in the prior 3 years
  • * Current enrollment in another study related to stroke or stroke recovery
  • * Any other medical contraindication to participation in the study, as evaluated by our team physician.
  • * Visual Analog of Pain Scale Score of 7 or greater

Ages Eligible for Study

18 Years to 84 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of California, Irvine,

David Reinkensmeyer, PhD, PRINCIPAL_INVESTIGATOR, University of California, Irvine

Study Record Dates

2026-01-29