Clinical trial
Wearable Devices Empowering Active Health Initiatives for High-Risk Stroke Populations
Recruiting now · Not applicable · 1 countries · Registry ID NCT06935513
Recruiting nowNot applicableInterventional
What this study is about
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
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age30 Years to Not listed
SexAll
Healthy volunteersNot accepted
ConditionHypertension, Diabetes, Atrial Fibrillation, Dyslipidemia, Smoking, Physical Inactivity, Obesity and Overweight
Full registry criteria
Inclusion Criteria: 1. Diagnosed with hypertension; 2. Diagnosed with diabetes; 3. Diagnosed with atrial fibrillation; 4. Smoking subjects; 5. Physical inactive subjects； 6. Obesity and overweight subjects; 7. Must be able to use smart wearable devices. Exclusion Criteria: 1. Diagnosed with malignancies; 2. Diagnosed with psychiatric disorders; 3. Diagnosed with cognitive impairment; 4. Unable to operate smart wearable devices.
Treatments and study arms
Wearable Devices
Behavioral
Participants utilize wearable devices (smart wristbands) 24 hours a day for 6 months. Wearable devices can provide medication reminders for each use and heart rate monitoring.
Primary outcomes
medication adherence and risk factor control rates6 months
1.The medication rates and control rates for hypertension; 2.The medication rates and control rates for hyperglycemia; 3. The medication rates and control rates for hyperlipidemia; 4.The medication rates and control rates for obesity.
Study locations
1 locations were listed when this page was built. The first 40 are shown.
Affiliated Hospital of Nantong University🇨🇳 Nantong, Jiangsu, China
Qiuhong Ji, MD, PhDContact
Tian Xu, MD, PhDContact