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Night recording of sleep for innovative sleep evaluation - NOCTIS

Nocturnal and circadian tracking for innovative sleep evaluation - NOCTIS - NOCTIS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58511
Enrollment
2500
Registered
2025-12-12
Start date
2026-10-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Sleep disorders Sleep disorders

Interventions

None listed

Sponsors

Kempenhaeghe
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Scheduled for a clinical PSG at Sleep Medicine Center KempenhaegheAge 18 years or olderAble to read and speak Dutch

Exclusion criteria

Exclusion criteria: Inability to provide informed consentInability to adhere to the study protocol (for example due to severe neurologic or psychiatric disorders) 

Design outcomes

Primary

MeasureTime frame
The main endpoint of this study is a database that includes raw PSG and wearable device data and clinical data from sleep disordered patients.

Countries

Netherlands

Contacts

Public ContactF. B. van Meulen

Kempenhaeghe

meulenf@kempenhaeghe.nl0402279022

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Apr 17, 2026