Breathing rate monitoring with a wearable device in patients with obstructive sleep apnea

Not Applicable

Completed

• Conditions: Obstructive sleep apnea; Nervous System Diseases; Sleep apnoea

• Registration Number: ISRCTN13965929
• Lead Sponsor: Stichting Haaglanden Clinics

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-03-11
• Study Start: 2021-09-06
• Last Update Posted: 20 September 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

1. Patients suspected of Obstructive Sleep Apnea scheduled for overnight respiratory polygraphy, and healthy volunteers
2. Aged 18 years or above

Exclusion Criteria

1. Wearer of cardiac implanted electronic device (Pacemaker, ICD)
2. CardioWatch 287 cannot be worn due to comprehensible reasons (allergic reactions, wounds, amputations, other)
3. Unable or not willing to sign informed consent
4. Significant mental or cognitive impairment
5. Currently enrolled in another clinical investigation in which the intervention might compromise the safety of the subject's participation in this study

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Respiration rate and heart rate as measured by the Corsano CardioWatch 287 and respiratory polygraphy, continuously for one night

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcome measures