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Risk prediction of circadian rhythm syndrome in occupational populations based on wearable devices and intervention of human-computer interaction health behaviors

Study on Health Behavioral Intervention for Metabolic Syndrome in Occupational Population Based on Wearable Devices

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076437
Enrollment
Unknown
Registered
2023-10-09
Start date
2023-10-09
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic syndrome

Interventions

Intervention group 1:Conduct real-time monitoring based on both wearable devices and smartphones, regularly collect physical examination indicator data every quarter, and conduct daily medical consult
Develop a health behavior intervention that combines the theory of information motivation behavioral skills.
Intervention group 2:Real time monitoring based on smartphones, regular collection of physical examination indicator data every quarter, and daily medical consultation
Control group 1:Real time monitoring is carried out based on both wearable devices and smartphones, with placebo intervention given, and regular collection of physical examination indicator data and d
Control group 2:Real time monitoring is carried out based on wearable devices, placebo intervention is given, and quarterly routine collection of physical examination indicator data and daily medical

Sponsors

Sichuan University West China School of Public Health and West China Fourth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Individuals over 18 years old; (2) Normal cognition and coordination with behavioral intervention; (3) Agree to participate in this experiment and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Have a previous history of cardiovascular and cerebrovascular diseases; (2) Patients with malignant tumors; (3) Pregnant or lactating women; (4) Participate in other similar experiments.

Design outcomes

Primary

MeasureTime frame
Mean metabolic equivalent;Sleep quality score;The amount of change in BMI;PHQ-9 change amount;CAD-7 change amount;

Secondary

MeasureTime frame
User satisfaction and compliance;

Countries

China

Contacts

Public ContactShujuan Yang

Sichuan University West China School of Public Health and West China Fourth Hospital

rekiny@126.com+86 189 8084 2145

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026