Last updated: January 2, 2024
Sponsor: University Hospital, Grenoble
Overall Status: Active - Recruiting
Phase
N/A
Condition
Sleep Apnea Syndromes
Treatment
Connected BORA Band to measure respiratory rate in COPD patients only
Connected tensiometer to measure arterial pressure
Epworth scale to evaluate sleepiness
Clinical Study ID
NCT04963192
2021-A01126-35
38RC21.149
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient with a chronic respiratory pathology such as:
- Newly diagnosed OSA with indication for CPAP treatment
- And/or COPD with or without indication for NIV/oxygen therapy
- Have a smartphone (with Android or iOS) allowing the installation of applications forconnected objects
- Be able to use a mobile application on a personal smartphone
- Person agreeing to the telemonitoring of CPAP or NIV/oxygen therapy compliance data bythe healthcare provider
- Patient who has provided consent to participate in the study
- Person affiliated to the social security
Exclusion
Exclusion Criteria:
- Pregnant or breastfeeding woman
- Patient unable to give consent to participate in the study
- Patient under guardianship or curatorship
- Patient not affiliated to the social security system
- Patient deprived of liberty or hospitalized
- Patient protected by law
- Patient under administrative or judicial control
- Patient currently participating in another clinical research study that may have animpact on the study, this impact is left to the discretion of the investigator
Study Design
Total Participants: 400
Treatment Group(s): 13
Primary Treatment: Connected BORA Band to measure respiratory rate in COPD patients only
Phase:
Study Start date:
September 10, 2021
Estimated Completion Date:
February 28, 2025
Study Description
Connect with a study center
Grenoble Alpes University Hospital
Grenoble, 38000
FranceSite Not Available
Verdun Hospital
Verdun, 55100
FranceActive - Recruiting

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