COVID-19 Surveillance Based on Smart Wearable Device

NCT ID: NCT04459637

Last Updated: 2022-03-28

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 103 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-08-02
• Study Completion Date: 2021-04-15

Brief Summary

This is a prospective, multi-center cohort study. 200 subjects with COVID-19will be included . Wearable device's physiological parameters and clinical data will be continually collected , the investigators aim to explore whether using smart wearable devices is useful to early alerting deterioration of COVID-19.

Detailed Description

This is a prospective cohort study. 200 subjects aged 18～75y with asymptomatic, mild, general-type COVID-19 will be recruited. The physiological parameters of wearable devices, including heart rate, sleep, blood oxygen saturation, electrocardiogram and exercise records, will be continuously collected from the day of admission / isolation to 14 days after discharge or out of quarantine. The Department of Respiratory and Critical Care of Peking University First Hospital is responsible for this research. All clinical data of patients during hospitalization will be collected including demographic characteristics, onset time, visit time, hospitalization time, symptoms, physical examination, laboratory examination, imaging characteristics, disease severity, treatment and outcome. Primary outcome is the deterioration of disease, the correlation analysis between the change of wearable device physiological parameters and the deterioration of disease determined by the traditional disease evaluation system will be used to find it whether can early alert deterioration of COVID-19.

The study protocol has been approved by the Peking University First Hospital Institutional Review Board (IRB) (2020-055). Any protocol modifications will be submitted for the IRB review and approval.

Conditions

COVID-19

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Asymptomatic group

Definition of asymptomatic disease:refer to Guidelines for the Diagnosis and Treatment of Novel Coronavirus Infection by the National Health Commission (Trial Version 7)

No interventions assigned to this group

Mild group

Definition of mild disease:refer to Guidelines for the Diagnosis and Treatment of Novel Coronavirus Infection by the National Health Commission (Trial Version 7)

No interventions assigned to this group

general-type group

Definition of general-type disease:refer to Guidelines for the Diagnosis and Treatment of Novel Coronavirus Infection by the National Health Commission (Trial Version 7)

No interventions assigned to this group

severe group

Definition of severe disease:refer to Guidelines for the Diagnosis and Treatment of Novel Coronavirus Infection by the National Health Commission (Trial Version 7)

No interventions assigned to this group

critical group

Definition of critical disease:refer to Guidelines for the Diagnosis and Treatment of Novel Coronavirus Infection by the National Health Commission (Trial Version 7)

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Age between 18 and 75 years(both 18 and 75), either gender;

2. At the time of enrollment, patients with novel coronavirus infection meeting the criteria of The New Coronavirus Pneumonia Diagnosis and Treatment Program (Seventh Edition)

3. Able to engage in daily activities;

4. Willing to participate in this research and willing to follow the research program, with the ability to sign informed consent;

5. having mobile communication equipment which can install APP of wearable device.

Exclusion Criteria

1. Wear time of wearable devices <50% during the whole study period

2. Wearable devices have faults, missing signals or errors throughout the study period, resulting in the proportion of analyzable information <50%

3. Patients with incomplete outpatient and inpatient information and missing core information such as hospitalization / discharge time, symptoms, laboratory examination, disease progress record, etc.

4. Patients with serious underlying diseases (including serious mental diseases, mental disorders, nervous system diseases, malignant tumors, chronic liver diseases, heart failure, autoimmune diseases, chronic kidney diseases), or life expectancy less than 6 months

5. Unable to take care of themselves in daily life, unable to cooperate with medical history and data collection

6. participating in other clinical trials;

7. Pregnant women, women in puerperium

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Peking University First Hospital

OTHER

Sponsor Role: lead

Responsible Party

Guangfa Wang

Professor & MD.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Peking University First Hospital

Beijing, Beijing Municipality, China

Countries

China

References

Zhang C, Sun A, Liao J, Zhang C, Yu K, Ma X, Wang G. COVID-19 surveillance based on consumer wearable devices. Digit Health. 2024 Apr 24;10:20552076241247374. doi: 10.1177/20552076241247374. eCollection 2024 Jan-Dec.

Reference Type: DERIVED

PMID: 38665889 (View on PubMed)

Other Identifiers

2020055-0615

Identifier Type: -

Identifier Source: org_study_id