Testing wearable devices to help manage stroke risk factors
Tests smart wearable devices in people at high risk of stroke.
Key facts
- Who runs it
- Affiliated Hospital of Nantong University
- Where
- Nantong, ChinaSee the site
- Trial code
- Registry title
- Wearable Devices Empowering Active Health Initiatives for High-Risk Stroke Populations
- Status
- Recruiting
- People taking part
- 300 people, planned
- Started
- 20 Apr 2025
- Planned end
- 20 Apr 2026
- Type of study
- Interventional, 2 groupsOne group gets no study treatment, for comparison.
- Treatments tested
- Wearable Devices
- Record updated
- 30 April 2025
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults at high risk of stroke, for example people with high blood pressure, diabetes, atrial fibrillation, smoking, little physical activity or overweight. They must be able to use a smart wearable device.
- Age
- 30 years or older
- Sex
- All sexes can join
- Disease stage
- Diagnosed with hypertension, diabetes or atrial fibrillation, or being a smoker, physically inactive, or obese or overweight
Main reasons for not taking part
- Diagnosed with a cancer (malignancy)
- Diagnosed with a psychiatric disorder
- Diagnosed with cognitive impairment
- Unable to operate smart wearable devices
The registry criteria, word for word
Show all 11 criteriaShow less
Who can take part
- Diagnosed with hypertension
- Diagnosed with diabetes
- Diagnosed with atrial fibrillation
- Smoking subjects
- Physical inactive subjects；
- Obesity and overweight subjects
- Must be able to use smart wearable devices
Who cannot take part
- Diagnosed with malignancies
- Diagnosed with psychiatric disorders
- Diagnosed with cognitive impairment
- Unable to operate smart wearable devices
Where in China
- Affiliated Hospital of Nantong UniversityNantong, ChinaContact: Qiuhong Ji, MD, PhDTaking people
About the trial
What the trial wants to find out
The purpose of this study is to evaluate the control effect of smart wearable devices on key risk factors in the high-risk populations for stroke
The 2 groups in the trial
- With Wearable DevicesTreatment being tested
Participants utilize wearable devices (smart wristbands) 24 hours a day for 6 months and receive medication reminders for each use and heart rate monitoring.
Treatment: Wearable Devices
- Without Wearable DevicesNo study treatment, for comparison
Participants do not utilize wearable devices (smart wristbands) .
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Wearable Devices Empowering Active Health Initiatives for High-Risk Stroke Populations
- Plain-language title
- Testing wearable devices to help manage stroke risk factorsGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Record updated
- 30 April 2025