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Wearable Devices in the Recovery Phase of Acute Exacerbations of COPD (AECOPDs)

NCT05776654 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21

Last updated 2024-05-29

No results posted yet for this study

Summary

The purpose the study is to successfully characterize the recovery phase of acute exacerbations of COPD in the outpatient setting using remotely captured physiologic data from wearable devices, to compare this with patient self-reported symptom data, to determine which physiologic variable(s) best correspond with AECOPD recovery, and to further document the feasibility, data quantity, data quality, and COPD outpatient usability experience with wearable devices.

Conditions

Interventions

DEVICE

Biometric wearable devices

Passive data collection using biometric wearable devices.

Sponsors & Collaborators

  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    lead OTHER

Principal Investigators

  • Bryan A. Ross, MD, FRCPC, MSc (Epi, Physiol) · Research Institute of the McGill University Health Centre (RI-MUHC)

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-16
Primary Completion
2024-01-15
Completion
2024-01-15

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT05776654 on ClinicalTrials.gov