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Recruiting NCT04219670

NCT04219670 Inpatient Stroke Recovery Using Sensors

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Clinical Trial Summary
NCT ID NCT04219670
Status Recruiting
Phase
Sponsor Shirley Ryan AbilityLab
Condition Stroke
Study Type OBSERVATIONAL
Enrollment 400 participants
Start Date 2017-10-31
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Wearable sensors

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 400 participants in total. It began in 2017-10-31 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

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

Contact & Investigator

Central Contact

Arun Jayaraman, PT, PhD

✉ a-jayaraman@northwestern.edu

📞 3122386875

Principal Investigator

Arun Jayaraman, PT, PhD

PRINCIPAL INVESTIGATOR

Study Principal Investigator

Frequently Asked Questions

Who can join the NCT04219670 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04219670 currently recruiting?

Yes, NCT04219670 is actively recruiting participants. Contact the research team at a-jayaraman@northwestern.edu for enrollment information.

Where is the NCT04219670 trial being conducted?

This trial is being conducted at Chicago, United States.

Who is sponsoring the NCT04219670 clinical trial?

NCT04219670 is sponsored by Shirley Ryan AbilityLab. The principal investigator is Arun Jayaraman, PT, PhD at Study Principal Investigator. The trial plans to enroll 400 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology