Phase
Condition
N/ATreatment
New telemonitoring approach using 2 connected devices : Scanwatch connected watch + Asten&masanté application
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult with newly diagnosed OSA (with central apnea index <5 ev/h), justifying CPAPand with low sleepiness (Epworth score <11 at inclusion).
Patient with at least 1 cardiovascular risk factor (obesity, type I or II diabeteswith or without treatment, permanent hypertension with or without treatment, heartfailure with preserved ejection fraction, valve disease, history of atrialfibrillation, history of ischaemic heart disease, history of stroke).
Patient with a smartphone and who agrees to use connected objects during the study.
Signed informed consent form,
Subject affiliated to a health insurance system, or is a beneficiary.
Exclusion
Exclusion Criteria:
Patients already fitted with a CPAP machine,
Patients with permanent atrial fibrillation,
Patients whose state of health is not stable or requires heavy treatment,
Patients with cognitive problems.
Patients participating in another intervention research in pulmonology.
Vulnerable subject
Study Design
Study Description
Connect with a study center
CHU Angers - Service de pneumologie
Angers, 49100
FranceActive - Recruiting
CHU Dijon-Bourgogne
Dijon, 21000
FranceActive - Recruiting
CH Départemental Vendée
La Roche-sur-Yon, 85925
FranceActive - Recruiting
CH Versailles
Le Chesnay, 78150
FranceActive - Recruiting
CH Le Mans
Le Mans, 72037
FranceActive - Recruiting
CHU Nancy
Nancy, 54511
FranceActive - Recruiting
AP-HP Bichat Claude Bernard
Paris, 75018
FranceActive - Recruiting
AP-HP Hôpital Européen Georges
Paris, 75015
FranceActive - Recruiting
AP-HP Pitié Salpêtrière
Paris, 75013
FranceActive - Recruiting
Polyclinique Saint-Laurent - Groupe médical de pneumologie
Rennes, 35000
FranceActive - Recruiting
CHU Rouen - Charles Nicolle
Rouen, 76000
FranceActive - Recruiting

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