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A Change in Diet May Decrease the Negative Consequences of Chronic Sleep Deprivation

Pilot Study: A Dietary Intervention May Decrease the Negative Metabolic and Cognitive Consequences of Chronic Sleep Deprivation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00123214
Enrollment
18
Registered
2005-07-22
Start date
2004-09-30
Completion date
2005-04-30
Last updated
2006-06-27

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

Conditions

Sleep Deprivation

Keywords

Diet, Chronic sleep deprivation, Weight, Cognitive impairment, Lipids, Inflammation, Resting metabolic rate, Weight Gain, Percent Body Fat, Hyperlipidemia

Brief summary

The purpose of this study is to determine whether or not a low calorie, low glycemic index diet with omega-3 fatty acid supplements can prevent some of the negative consequences of sleep deprivation.

Detailed description

This pilot study included 18 medical residents at two academic medical centers in New York City. All residents who participated in the study were assigned to work a night shift schedule for two weeks, and began the study on the morning prior to their first evening shift. The study subjects were randomly assigned to one of two groups: * Intervention diet -- consisting of 40% carbohydrates, 30% protein, and 30% fat with 2.4g of long chain fatty acid supplements (n=9) Total calories for males was 1600/day, and 1200/day for females * Control group -- ad lib diet. Main outcome measures included: * weight * resting metabolic rate * percent body fat * lipid profile * CRP * fasting glucose and insulin levels * urinary neurotransmitter levels * salivary cortisol * six cognitive tests of memory, attention, and executive function. Subjects were tested on day 1, 7, and 14 of the study.

Interventions

Sponsors

Inflammation Research Foundation, Marblehead, MA.
CollaboratorUNKNOWN
NeuroScience, Inc., Osceola, WI.
CollaboratorINDUSTRY
St. Vincent's Medical Center
Lead SponsorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Medical resident in good standing at Cabrini Medical Center or Saint Vincent's Hospital, NY. * Must be scheduled for two consecutive weeks of night shift work.

Exclusion criteria

* Febrile illness * Smoker * Food allergies of any kind * Taking any prescription medication * History of diabetes or thyroid dysfunction * Body mass index (BMI)\>30 * Pregnancy

Design outcomes

Primary

MeasureTime frame
Resting Metabolic Rate

Secondary

MeasureTime frame
Percent Body Fat
Waist Circumference
Lipid Profile
C-reactive Protein Levels
Weight
Fasting serum insulin
Urinary neurotransmitter levels
Salivary a.m. cortisol levels
Cognitive scores on: Stroop Test, Hopkins Verbal Learning Test, Trail Making Test, Digit Span, Block Design, Dynamic Visual Acuity, Short Form 36
Fasting serum glucose

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026