Evaluation of the comfort and usability of two different sleep EEG devices in a home environment

Evaluation of the comfort and usability of two different sleep EEG devices in a home environment - SleepWell_Komfort

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028525

Enrollment

Registered

2022-03-25

Start date

2022-03-30

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

sleep quality

Interventions

Group 1: Observational study: healthy participants are asked to evaluate the user-friendliness and comfort of two commercially available sleep monitoring systems for the home environment. The two syst

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: - Fully vaccinated against Covid-19 - Age: 18-85 - Understanding of the German or English language

Exclusion criteria

Exclusion criteria: - Magnetizable metal in the brain / skull - History of seizure disorders (epilepsy) / family history - Neurological diseases

Design outcomes

Primary

Measure	Time frame
comparison of two commercially available sleep monitoring systems for the home environment.	—

Countries

Germany

Contacts

Public ContactAxel Winneke

Fraunhofer IDMT

axel.winneke@idmt.fraunhofer.de044136116842

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026