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Development and Clinical Application of Perioperative Intelligent Health Education Digital Intervention Mini-program Based on Four-Dimensional Risk Stratification and AI Prediction Model

Development and Clinical Application of Perioperative Intelligent Health Education Digital Intervention Mini-program Based on Four-Dimensional Risk Stratification and AI Prediction Model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128830
Enrollment
Unknown
Registered
2026-07-27
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Perioperative multiple systemic complications induced by surgical and anesthetic procedures, including perioperative hypothermia, intraoperative hypotension, postoperative acute kidney injury, postoperative delirium, anesthetic emergence agitation, postoperative nausea and vomiting, postoperative pulmonary complications.

Interventions

Observation group with precise intervention via AI mini-program:Perioperative hierarchical intervention based on WeChat mini-program with AI risk prediction
Control group with routine perioperative management:Traditional paper-based perioperative risk assessment and health education nursing

Sponsors

Nanjing Luhe People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old, scheduled inpatient surgery; 2.Plan to receive general anesthesia or neuraxial anesthesia; 3.Able to complete questionnaires and WeChat mini-program operations (family members may assist); 4.Patients or legal representatives voluntarily sign written informed consent; 5.Complete clinical medical records and anesthesia baseline data can be collected.

Exclusion criteria

Exclusion criteria: 1.Patients under emergency rescue or traumatic emergency surgery; 2.Pre-existing end-stage renal disease, persistent hypothermia, severe cognitive impairment or coma; 3.Complete loss of visual and auditory function without family assistance to complete the study; 4.Those who refuse to participate or withdraw from the study midway; 5.Patients with severe missing key laboratory and anesthesia record data.

Design outcomes

Primary

MeasureTime frame
Composite perioperative adverse events;

Secondary

MeasureTime frame
Health education adherence rate;Patient hospitalization satisfaction score;Preoperative assessment time consumption;Preoperative anxiety score;

Countries

China

Contacts

Public ContactWang Peng

Nanjing Luhe People's Hospital

wp19780716@126.com+86 25 57129179

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026