Wearable Accelerometers for Predicting Perioperative Risk in Elderly Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorPeking Union Medical College Hospital

About this trial

This single-center prospective cohort study is designed to evaluate whether preoperative physical activity measured by a wearable accelerometer is associated with cardiovascular autonomic function and whether it can help predict post-induction hypotension in elderly patients undergoing elective non-cardiac surgery. Patients aged 65 years or older scheduled for general anesthesia with tracheal intubation will undergo preoperative physical activity monitoring using an ActiGraph wearable accelerometer. Activity-related parameters, including sedentary time, light-, moderate-, and vigorous-intensity activity, daily step count, and sleep duration, will be recorded. Cardiovascular autonomic function will be assessed perioperatively using noninvasive continuous hemodynamic monitoring, with baroreflex sensitivity-related indices derived from continuous blood pressure and beat-to-beat timing data. The primary outcome is post-induction hypotension. Secondary outcomes include early intraoperative hypotension, postoperative complications, and 30-day mortality. This study aims to clarify the relationship between habitual physical activity and autonomic regulation in older surgical patients and to provide evidence supporting future prehabilitation strategies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥65 years

Scheduled for elective non-cardiac surgery

American Society of Anesthesiologists (ASA) physical status I-III

Planned to undergo general anesthesia

Disqualifiers

Severe vascular disease

Secondary hypertension

Limb tremor disorders, such as Parkinson disease

Inability to wear a wrist-based wearable accelerometer for any reason

Trial population

Elderly patients who will undergo general anesthesia surgery in Peking Union Medical College Hospital.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: observational group

Trial outcomes

Primary outcomes

1

Post induction hypotension

Systolic blood pressure less than 90 mmHg, mean arterial pressure less than 65 mmHg, or a decrease of more than 30% from baseline.

Time frame
Within 20 minutes after induction of anesthesia or before surgical incision.
2

Early intraoperative hypotension

Systolic blood pressure less than 90 mmHg, mean arterial pressure less than 65 mmHg, or a decrease of more than 30% from baseline.

Time frame
Within 30 minutes after incision

Secondary outcomes

1

Postoperative complications

We use Clavien-Dindo system to grade postoperative complications

Time frame
Within 30 days after surgery

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.