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Conditioning of the Cortisol Awakening Response (CAR)

Conditioning of the Cortisol Awakening Response (CAR) - CAR Conditioning

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50199
Enrollment
88
Registered
2018-04-03
Start date
2018-04-23
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Het onderzoek wordt bij gezonde mensen uitgevoerd. Uitkomsten uit deze lijn van onderzoek bieden nieuwe handvatten voor therapeutische interventies voor patiënten met verlate slaap-fase syndroom of seizoensgebonden depressie. Not applicable

Interventions

The intervention consists of a conditioning paradigm, in which as association is learned between a scent and the circadian CAR. See Study design of the summary for the description of this paradigm.

Sponsors

Universiteit Leiden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Male gender * Aged between 21 and 34 years of age * Good understanding of written and spoken Dutch.

Exclusion criteria

Exclusion criteria: * Refusal to give written informed consent * Severe somatic or psychiatric conditions that would adversely affect participant*s safety or that might interfere with the study protocol * Olfactory impairments * Known sensitivity or hypervigilance to one of the ingredients of the scents used in this experiment * Heavy use of (illegal) drugs including cannabis and habits of heavy drinking * Irregular sleep pattern or sleep problems * Use of medication that interferes with the study protocol * Factors known to influence the CAR: o Having an acute illness, or experienced an illness in the past seven days (e.g. influenza, common cold) o Experienced jet lag or shift work in the past seven days o Use of (oral) glucocorticoid medication o HPA-axis related endocrine disorders (e.g., Cushings disease or Addisons disease) o Brain damage, particularly hippocampal brain damage o Obesity

Design outcomes

Primary

MeasureTime frame
The main study parameter is change in the CAR (evocation measurement compared to baseline measurement) in the experimental compared with the control group.

Secondary

MeasureTime frame
Secondary outcomes are physiological parameters (e.g. HR), and psychological parameters (e.g. affect).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)