Predicting Exacerbation of COPD With Wireless Telemonitoring

NCT ID: NCT02791451

Last Updated: 2021-04-15

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-10-31
• Study Completion Date: 2017-12-31

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.

Conditions

COPD

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Telemonitoring

Exacerbation of COPD with wireless telemonitoring of respiratory rate, heart rate and sleep.

Group Type: EXPERIMENTAL

telemonitoring

Intervention Type: DEVICE

To predict exacerbation of COPD with wireless telemonitoring

Interventions

telemonitoring

To predict exacerbation of COPD with wireless telemonitoring

Intervention Type: DEVICE

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Turku

OTHER

Sponsor Role: collaborator

Turku University Hospital

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

COPD_BCG

Identifier Type: -

Identifier Source: org_study_id