Sepsis
Conditions
Interventions
Intervention Group:Intervention Group: Wearing smart wearable devices (collecting vital signs such as heart rate, blood oxygen, body temperature, blood pressure) + AI-based remote monitoring and rehab
Control Group:Control Group: Routine health education + telephone follow-up (without smart device intervention).
Sponsors
Affiliated Hospital of Jiangsu University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Meeting the Sepsis-3.0 diagnostic criteria for sepsis with low mortality risk within 28 days after discharge; 2. Aged >=18 years old, regardless of gender; 3. Having complete clinical data (including diagnosis, laboratory tests, treatment history, etc.); 4. Being proficient in using smart wearable devices/mobile APPs, or having family members to assist in operation; 5. Signing the informed consent form and voluntarily participating in the study.
Exclusion criteria
Exclusion criteria: 1. Not meeting the sepsis diagnostic criteria or having controversial diagnosis; 2. Aged <18 years old; 3. Complicated with cognitive impairment, mental illness, or being unable to cooperate with the study process/with extremely poor compliance; 4. Unable to maintain long-term follow-up contact with high risk of loss; 5. Expected survival time <28 days, or complicated with severe malignant tumors or end-stage organ failure; 6. Refusing to participate in the study or wear smart wearable devices; 7. Having contraindications for smart device use (such as severe skin allergy)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 12-month Survival Rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Readmission Rate;Outpatient Visit Rate;ED Visit Rate;Quality of Life (EQ-5D-5L); | — |
Countries
China
Contacts
Public ContactJianguo Zhang
Affiliated Hospital of Jiangsu University
Outcome results
None listed