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Evaluation of Compumedics Somfit Device

Performance Evaluation of the Compumedics Somfit Sleep Monitoring Device

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04326127
Enrollment
30
Registered
2020-03-30
Start date
2019-11-06
Completion date
2019-11-19
Last updated
2020-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea

Brief summary

To study whether Somfit is substantially equivalent to an existing approved device (i.e. Compumedic's Grael System) to assist in elucidating sleep disorders.

Detailed description

Sleep is recognized as one of the three pillars of health (i.e. nutrition, exercise and sleep). Poor quality and fragmented sleep leads to an increase in the risk for development of chronic health conditions. Given the importance of good quality sleep and its critical role in overall well-being, there is a need for regular monitoring and assessment of sleep quality in individuals. However, current technologies will only allow for this to be performed in sleep clinics and with the help of full polysomnography (PSG) systems which require the patients to spend a night at the clinic with several wired electrodes connected to their scalp. This will cause discomfort for the patients in a long run. To solve this problem, Compumedics has recently developed a miniaturized, portable and affordable sleep monitoring system with code name of Somfit which can be used in the comfort of patients' home. The aim of this study is to validate Somfit for home based sleep studies.

Interventions

DEVICEIntervention is the validation of a sleep monitoring device (i.e. Somfit) against the gold-standard polysomnograph with electroencephalograph (i.e. the Greal system)

Data were recorded overnight by both devices simultaneously

Sponsors

Compumedics Limited
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Individuals age between 18 to 75 * Be able to give informed consent * Individuals with diagnosed Obstructive Sleep Apnoea (OSA)

Exclusion criteria

* Less than 18 years of age * Greater than 75 years of age * Unable or not willing to provide informed consent * Need for nursing care * Currently working nightshift

Design outcomes

Primary

MeasureTime frameDescription
Comparison between raw EEG signalssingle night recording for each subjectDirect comparison of Raw EEG data between Somfit and Grael system on an epoch by epoch basis (with each epoch being equivalent to 30 secs) to test and validate Somfit for data acquisition, display and record of Raw EEG data.

Secondary

MeasureTime frameDescription
Comparison between Manual and Automatic sleep Scoring - Sleep hypnogramsingle night recording for each subjectEpoch-by-epoch comparison between manual and automatic scoring of sleep data recorded by Somfit and Grael devices

Other

MeasureTime frameDescription
Validation of the new device for detection of sleep apneasingle night recording for each subjectDifferentiation between case and control groups

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026