Predicting Exacerbation of COPD With Wireless Telemonitoring

Not Applicable

Terminated

• Conditions: COPD
• Interventions: Device: telemonitoring

• Registration Number: NCT02791451
• Lead Sponsor: Turku University Hospital

Brief Summary

This is an open-label single-center 6-month prospective clinical trial predicting exacerbation of COPD with wireless telemonitoring of respiratory rate, heart rate and sleep in patients admitted to the pulmonary ward of the Turku University Hospital due to acute exacerbation of COPD.

Detailed Description

A bed sensor based on ballistocardiogram (BCG) will be used to wireless telemonitoring of respiratory rate, heart rate and sleep for six months after an acute exacerbation of COPD.

Study Timeline

• Study First Submitted: 2016-06-01
• Study First Submitted QC: 2016-06-01
• Study First Posted: 2016-06-06
• Study Start: 2016-10
• Primary Completion: 2017-12
• Study Completion: 2017-12
• Status Verified: 2021-04
• Last Update Submitted: 2021-04-12
• Last Update Posted: 2021-04-15

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

• Consecutive patients treated due to acute exacerbation of COPD at the pulmonary wards of the Turku University Hospital

Exclusion Criteria

• Those sleeping with a bed partner and not having separate mattresses
• Patients with pacemaker

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Telemonitoring	telemonitoring	Exacerbation of COPD with wireless telemonitoring of respiratory rate, heart rate and sleep.

Primary Outcome Measures

Name	Time	Method
Time window to detect acute exacerbation of COPD	Six months	Time window to detect acute exacerbation of COPD