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One night of partial sleep restriction: effects on metabolism, mood and stress responsiveness

One night of partial sleep restriction: effects on metabolism, mood and stress responsiveness - Metabolism and stress after one night of partial sleep restriction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43632
Enrollment
36
Registered
2016-03-29
Start date
2016-06-10
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Lipid metabolism obesity

Interventions

A single night of short sleep duration (4 hours) compared to a control condition of normal sleep duration (8 hours).

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Informed consent - Caucasian men - Age between 18 and 55 years - BMI between 20 and 25 kg/m2 (equally divided over the range, so ideally n=12 in BMI categories 20 -25; 25 - 30; 30 - 35 kg/m2)

Exclusion criteria

Exclusion criteria: Active endocrine disease (e.g. diabetes mellitus type 1 and type 2, thyroid disease, Cushing*s disease and lipid-associated disorders such as FH) - Fasting glucose >7.0 mmol/L - Severe chronic disease (e.g. chronic liver or kidney disease) - Severe insomnia, sleep disorders or exceptional habitual sleep duration (10 h). - Medication use including the following: lipid lowering drugs, glucocorticoids, sleep medication, hormone replacement, glucose lowering drugs, insulin therapy (last 6 weeks), anticoagulants - Recent time zone travel (last 6 weeks) - Shift work (last 6 weeks) - Severe alcohol use (>21 units/week) - Psychiatric disease - Drug abuse - Recent participation to another nutritional or biomedical trial (last 6 weeks) - Taking medication, which may interfere with study measurements, as judged by the responsible physician - Reported weight loss or weight gain (10%) in the last six months prior to the pre-study screening - Clinically relevant abnormalities in clinical chemistry at screening (to be judged by the study physician) - Reported use of any nicotine containing products in the six months preceding the study and during the study itself; - Extreme strenuous exercise during last 3 months, as judged by responsible physician - Excessive sunbathing during the last 3 months, as judged by responsible physician

Design outcomes

Primary

MeasureTime frame
The primairy study parameters are: - Lipid metabolism by measurement of hormone and lipid concentrations in plasma in response to a mixed-meal challenge - Energy metabolism by measurement of indirect calorimetry - HPA-axis responsiveness by hormone and blood pressure measurement during a cold- feet pressor test - Mood via short questionnaires (Profile of Mood States)

Secondary

MeasureTime frame
The secondairy study parameters are: - Gene expression profiles and metabolomics in muscle and fat tissue and plasma - Gene expression profiles in skin and hair samples

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)