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Wearable Devices Empowering Active Health Initiatives for High-Risk Stroke Populations (AISP)

A

Affiliated Hospital of Nantong University

Status

Enrolling

Conditions

Hypertension
Physical Inactivity
Atrial Fibrillation
Obesity and Overweight
Diabetes
Dyslipidemia
Smoking

Treatments

Behavioral: Wearable Devices

Study type

Interventional

Funder types

Other

Identifiers

NCT06935513
2025005

Details and patient eligibility

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

Full description

A randomized controlled study was conducted on the application of smart wearable devices in the intervention of high-risk populations for stroke, with a focus on whether the functions of smart wearable devices such as medication reminders, heart rate monitoring, and exercise reminders can effectively benefit the improvement of key risk factors for stroke, especially blood pressure, blood glucose, and blood lipids.

Enrollment

300 estimated patients

Sex

All

Ages

30+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

With Wearable Devices
Experimental group
Description:
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:
Behavioral: Wearable Devices
Without Wearable Devices
No Intervention group
Description:
Participants do not utilize wearable devices (smart wristbands) .

Trial contacts and locations

1

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Central trial contact

Qiuhong Ji, MD, PhD; Pengyu Gong, MD

Data sourced from clinicaltrials.gov

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