RECRUITING

Inpatient Stroke Recovery Using Sensors

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Conditions

StrokeDevice StudiesNoninvasive ProceduresDevice FeasibilityInpatient RehabilitationSensorsMachine Learning

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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

This observational trial seeks to assess the feasibility of using non-invasive, portable, real-time body-worn sensors to continuously monitor, quantify, and interpret recovery during inpatient treatment of stroke

Official Title

Wearable Sensor Platform to Monitor Stroke Recovery During Inpatient Rehabilitation

Quick Facts

Study Start:2017-10-31
Study Completion:2024-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04219670

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patient group
  2. * Individuals diagnosed with stroke admitted to the Shirley Ryan AbilityLab (inpatient), or individuals in the community who had a stroke (chronic)
  3. * Age 18 or older
  4. * Able and willing to give written consent and comply with study procedures
  5. * Healthy control group
  6. * Individuals without any known significant health problem (healthy controls)
  7. * Age 18 or older
  8. * Able and willing to give written consent and comply with study procedures
  1. * Patient group
  2. * Neurological degenerative pathologies as co-morbidities (such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, etc.)
  3. * Pregnant or nursing
  4. * Skin allergies or irritation; open wounds
  5. * Utilizing a powered, implanted cardiac device for monitoring or supporting heart function (i.e. pacemaker, defibrillator, or LVAD)
  6. * Healthy control group
  7. * No known history of cerebrovascular accidents or neurological degenerative pathologies (such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, etc.)
  8. * Pregnant or nursing
  9. * Skin allergies or irritation; open wounds
  10. * Utilizing a powered, implanted cardiac device for monitoring or supporting heart function (i.e. pacemaker, defibrillator, or LVAD)

Contacts and Locations

Study Contact

Arun Jayaraman, PT, PhD
CONTACT
3122386875
a-jayaraman@northwestern.edu
Sara Prokup, PT, DPT
CONTACT
3122381355
sprokup@ricres.org

Principal Investigator

Arun Jayaraman, PT, PhD
PRINCIPAL_INVESTIGATOR
Study Principal Investigator

Study Locations (Sites)

Shirley Ryan AbilityLab
Chicago, Illinois, 60611
United States

Collaborators and Investigators

Sponsor: Shirley Ryan AbilityLab

  • Arun Jayaraman, PT, PhD, PRINCIPAL_INVESTIGATOR, Study Principal Investigator

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 Date2017-10-31
Study Completion Date2024-09

Study Record Updates

Study Start Date2017-10-31
Study Completion Date2024-09

Terms related to this study

Keywords Provided by Researchers

  • Stroke
  • Device Studies
  • Noninvasive Procedures
  • Device Feasibility
  • Inpatient Rehabilitation
  • Sensors
  • Machine Learning

Additional Relevant MeSH Terms

  • Stroke