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Circadian Data Collection from Sleep-Onset Insomnia Patients

Circadian Data Collection from Sleep-Onset Insomnia Patients - CDC_SOIP

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00005629
Enrollment
20
Registered
2014-01-21
Start date
2014-01-20
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

G47.0 G47.2

Interventions

Group 1: circadian data from sleep-onset insomnia patients

Sponsors

Philips Research Eindhoven
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosed sleep-onset insomnia

Exclusion criteria

Exclusion criteria: Diagnosed neurological, psychiatric, cardiovascular disorders. Diagnosed sleep apnea or restless legs syndrome. Use of sleep or antidepressants. Shift workers. Caretaker of babies or small children. Having travelled across 2 or more time yones in the past 2 weeks. Drug or excessive alcohol consumption. Caffeine consumption above 350mg per day. Frequent exercisers (>4hours/week).

Design outcomes

Primary

MeasureTime frame
The ECG and actigraphy data will be used to train and test mathematical models to estimate circadian phase. The output of the models will be compared to the reference value, DLMO.

Secondary

MeasureTime frame
Insights into the differences in HRV features in healthy versus sleep-onset insomnia patients will be assessed.

Countries

Germany

Contacts

Public ContactEnrique Gil

Philips Research

enrique.gil@philips.com+31631784276

Outcome results

None listed

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