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
| Type | Name | Description |
|---|---|---|
| OTHER | Aerobic training | 5 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.