RECRUITING

Wearable Device and Behavioral Support for Enhancing Arm Use After Stroke

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Conditions

Chronic Stroke PatientsSensorSmartWatchStroke RecoveryStroke RehabilitationMotivational Interviewing

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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

Official Title

Sensor Enhanced Activity Motivation After Stroke

Quick Facts

Study Start:2025-08-20
Study Completion:2026-01-29
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07042152

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.

Ages Eligible for Study:18 Years to 84 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 to 85 years of age
  2. * Experienced a single or multiple, ischemic or hemorrhagic stroke, with unilateral weakness, over six months previously
  3. * 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.
  4. * Absence of major depression, as defined by DSM V criteria or a score on the Geriatric Depression Scale \< 10.
  1. * Any substantial decrease in alertness, language reception, or attention
  2. * Single or multiple, ischemic or hemorrhagic stroke less than 6 months ago
  3. * Severe muscle tone at the upper extremity (score ≥ 3 on the Modified Ashworth Spasticity scale)
  4. * Pregnant or lactating
  5. * Advanced liver, kidney, cardiac, or pulmonary disease
  6. * Coexistent major neurological disease
  7. * Coexistent major psychiatric disease
  8. * Plans to alter any current participation in other rehabilitation therapy in the time period of the study
  9. * A terminal medical diagnosis consistent with survival \< 1 year
  10. * A history of significant alcohol or drug abuse in the prior 3 years
  11. * Current enrollment in another study related to stroke or stroke recovery
  12. * Any other medical contraindication to participation in the study, as evaluated by our team physician.
  13. * Visual Analog of Pain Scale Score of 7 or greater

Contacts and Locations

Study Contact

Vicky Chan, DPT
CONTACT
9498248423
vchan2@uci.edu
Natanya Gunn, Medical Student
CONTACT
natanyag@hs.uci.edu

Principal Investigator

David Reinkensmeyer, PhD
PRINCIPAL_INVESTIGATOR
University of California, Irvine

Study Locations (Sites)

University of California Irvine
Irvine, California, 92697
United States

Collaborators and Investigators

Sponsor: University of California, Irvine

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-08-20
Study Completion Date2026-01-29

Study Record Updates

Study Start Date2025-08-20
Study Completion Date2026-01-29

Terms related to this study

Keywords Provided by Researchers

  • Sensor
  • SmartWatch
  • Stroke Recovery
  • Stroke Rehabilitation
  • Motivational Interviewing

Additional Relevant MeSH Terms

  • Chronic Stroke Patients