A study on the Bonsai Sensor on participants with or without Obstructive Sleep Apnoea (OSA) to assess signal parameters

Not Applicable

• Conditions: /A; N/A; Respiratory - Sleep apnoea

• Registration Number: ACTRN12624000847516
• Lead Sponsor: ResMed Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-07-09
• Last Update Posted: 15 July 2024

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Participants willing to give written informed consent
Participants who >/= 18 years of age
Participants who are willing test the sensors for 3 nights, and up to 5 nights
Participants owning an iPhone (generation 7 and later) on which the participant can download the app used for the study
(Obstructive Sleep Apnoea (OSA). Participants in this study may or may not have OSA); Participants willing to give written informed consent
Participants who >/= 18 years of age
Participants who are willing test the sensors for 3 nights, and up to 5 nights
Participants owning an iPhone (generation 7 and later) on which the participant can download the app used for the study
(Obstructive Sleep Apnoea (OSA). Participants in this study may or may not have OSA)

Exclusion Criteria

Participants who are or may be pregnant
Participants with clinically relevant peripheral vascular disease, such as secondary Raynaud’s disease.
Participants believed to be unsuitable for inclusion by the researcher
; Participants who are or may be pregnant
Participants with clinically relevant peripheral vascular disease, such as secondary Raynaud’s disease.
Participants believed to be unsuitable for inclusion by the researcher

Study & Design

• Study Type: Interventional
• Study Design: Not specified