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NCT02791451 Clinical Trial

Predicting Exacerbation of COPD With Wireless Telemonitoring

COPD Clinical Trial

Official title:
Open-Label Prospective Study of Predicting Exacerbation of Chronic Obstructive Pulmonary Disease (COPD) With Wireless Telemonitoring of Respiratory Rate, Heart Rate and Sleep

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02791451
Other study ID # COPD_BCG
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date December 2017

Study information
Verified date April 2021
Source Turku University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Terminated
Enrollment 6
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Device:
• telemonitoring
To predict exacerbation of COPD with wireless telemonitoring

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Turku University Hospital University of Turku

Outcome
Type Measure Description Time frame Safety issue
Primary Time window to detect acute exacerbation of COPD Time window to detect acute exacerbation of COPD Six months
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