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The use of wearable continuous monitoring devices in the perioperative period in elderly hip fracture patients

The use of wearable continuous monitoring devices in the perioperative period in elderly hip fracture patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078687
Enrollment
Unknown
Registered
2023-12-15
Start date
2024-01-01
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

elderly hip fracture patients

Interventions

Group W:Acceptance of wearable continuous monitoring equipment
Group C:Acceptance of routine monitoring equipment

Sponsors

The First Affiliated Hospital of USTC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Elective hip fracture surgery; 2) ASA grade I to III; 3) Signed informed consent. 4) Age = 65 years old

Exclusion criteria

Exclusion criteria: 1) Implantation of a cardioverter defibrillator or pacemaker; 2) Hypersensitivity to the study device; 3) Severe cognitive impairment as assessed by the Brief Mental State Examination (MMSE) or inability to cooperate with wearing a wireless monitoring device; 4) Patients with schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis.

Design outcomes

Primary

MeasureTime frame
Number of postoperative adverse events;—

Secondary

MeasureTime frame
Number of interventions based on MEWS scores;Patient and nurse satisfaction;Time to accumulate abnormal vital signs;Frequency of abnormal vital signs;—

Countries

China

Contacts

Public ContactHe keqiang

The First Affiliated Hospital of USTC

doctorhector@ustc.edu.cn+86 189 5519 7569

Outcome results

None listed

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