Clinical Trials Directory

Trials / Completed

CompletedNCT03004716

Telemonitoring in Pulmonary Rehabilitation: Validity of a Remote Pulse Oxymetry System

Status
Completed
Phase
Study type
Observational
Enrollment
5 (actual)
Sponsor
ADIR Association · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the feasibility and the reliability of a telemonitoring system during pulmonary rehabilitation in patients with chronicle obstructive pulmonary disease. The feasibility is assessed using the patient's satisfaction and it ease of use. The reliability of the remote telemonitoring system is assessed comparing the local data (extracted from the monitoring device itself) and the data transmitted through the telemonitoring platform.

Conditions

Interventions

TypeNameDescription
OTHERAerobic training5 consecutive patients with chronicle obstructive pulmonary disease are offered to participate in the protocol when they have reached 45 min of aerobic training during their pulmonary rehabilitation program. During 5 sessions of 45 min, they are monitored with an oximeter device (Nonin 3150) which records heart rate (HR) and oxygen transcutaneous saturation (SpO2). The device also communicates with a telemedicine medical gateway which sends these data to a remote telemedicine center. Data are then provided on a secured online platform and compared with data recorded on the device (Nonin 3150).

Timeline

Start date
2017-01-01
Primary completion
2017-03-01
Completion
2017-03-01
First posted
2016-12-29
Last updated
2017-03-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03004716. Inclusion in this directory is not an endorsement.