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The RuiLink digital health monitoring program based on wearable devices and mobile applications

The RuiLink digital health monitoring program based on wearable devices and mobile applications

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121198
Enrollment
Unknown
Registered
2026-03-26
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

None

Interventions

Observation group:NA

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 18 years old or above; 2. Being permanent residents of the area, who have resided locally for at least 4 months in the past 6 months, and planing to stay in the long term; 3. Possessing or being willing to use smartphones that meet the requirements, and wearing and using the designated wearable devices as instructed, Having basic operating skills for smartphones, or being able to complete the operations with the assistance of family members; 4.Agreeing to undergo regular or irregular follow-up contacts during the study period, which shall last for at least 5 years; 5. Voluntarily participating in this study and signing the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Planing to relocate from the target research area within the next two years; 2. Suffering from severe diseases or terminal illnesses, with an expected lifespan of less than 2 years, such as cancer, terminal heart failure, kidney failure, etc. 3.Being incompliant to use of wearable devices, or in situations that may affect the operation of the devices, including cognitive dysfunction, visual impairment, limb movement disorder, disability, burns, tattoos, skin diseases, allergies to device materials, after implantation of a cardiac pacemaker, after implantation of a cardioverter-defibrillator, after implantation of an artificial cochlea, etc. 4. Currently participating in other clinical studies; 5. Co-morbid with mental illnesses or behavioral problems, being unable to understand the requirements of the study or cooperate in completing the long-term follow-up, or any other circumstances that affect the participant's safety, data quality, or the integrity of the study; 6. Other circumstances that might affect the study compliance according to the researcher;

Design outcomes

Primary

MeasureTime frame
diastolic blood pressure;Smoke;Heart rate;temperature;Electrocardiogram-related parameters;Sleep-related parameters;oxygen saturation;Physical activity-related parameters and sedentary time;drink;respiratory rate;basal metabolic rate;sports;systolic pressure;quality of life;diet;

Countries

China

Contacts

Public ContactYufang Bi

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

byf10784@rjh.com.cn+86 21 5466 1789

Outcome results

None listed

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