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Wearable Health Technology for Perioperative Risk Assessment

NCT05083598 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2022-11-30

No results posted yet for this study

Summary

Accurate and timely preoperative identification of high-risk patients provides opportunities to better inform and manage them. Current predictors for perioperative complications are either resource consuming or have low accuracy. The primary objective of the study is to assess if Wearable Devices may be an alternative to assess cardiopulmonary function, with low risks and lower costs.

Conditions

  • Surgery--Complications

Interventions

OTHER

6 Minute walking test

The patient is asked to repetitively walk along a 15 m track, at their best speed, in six minutes. Before and after the exercise, blood arterial pressure and dyspnea level (via Borg scale) are assessed. Cardiac frequency and peripheral Oxygen saturation are assessed before the test, and every minute and in the two minutes following the exercise.

OTHER

Frailty questionaires

Clinical Frailty Score, Metabolic Equivalent of Task, DUKE Activity Status Index

Sponsors & Collaborators

  • Politecnico di Milano

    collaborator OTHER

  • Istituto Clinico Humanitas

    lead OTHER

Eligibility

Min Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-10
Primary Completion
2022-06-30
Completion
2022-07-30

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05083598 on ClinicalTrials.gov