Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
100 participants
INTERVENTIONAL
2020-12-14
2026-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Day worker
Men and women who work only day shift for at least 3 consecutive days of the week
Portion size
The amount of food served (g) at the first two meals of each day. These amounts will vary across 4 weeks.
Night worker
Men and women who work only night shift for at least 3 consecutive days of the week
Portion size
The amount of food served (g) at the first two meals of each day. These amounts will vary across 4 weeks.
Interventions
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Portion size
The amount of food served (g) at the first two meals of each day. These amounts will vary across 4 weeks.
Eligibility Criteria
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Inclusion Criteria
* BMI 19-35 kg/m\^2
* Age 20-55 years of age
* Metabolically healthy
* Weight stable over previous 3 months
* Lives in New York City area
Exclusion Criteria
* Smoking
* History of drug or alcohol abuse
* Rotating shift work
* Habitual sleep duration of more than 6 hour per night
* Obstructive sleep apnea
* Transmeridian travel
* Type 2 diabetes
* Cardiovascular disease
* Hypertension
* Participation in diet or weight loss program in the 3 months prior to enrollment
* Psychiatric or sleep disorder
* Food allergies or intolerances
* Dislike of or unwillingness to eat test foods
20 Years
55 Years
ALL
Yes
Sponsors
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Columbia University
OTHER
Responsible Party
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Marie-Pierre St-Onge
Associate Professor of Nutritional Medicine
Principal Investigators
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Faris M Zuraikat, PhD
Role: PRINCIPAL_INVESTIGATOR
Columbia University
Marie-Pierre St-Onge, PhD
Role: PRINCIPAL_INVESTIGATOR
Columbia University
Locations
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Columbia University Irving Medical Center
New York, New York, United States
Countries
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Other Identifiers
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AAAS8559
Identifier Type: -
Identifier Source: org_study_id
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