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Eating Behaviors in Shift Workers

The Interaction of Shift Work and Food Environment on Eating Behaviors and Appetite

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04468672
Enrollment
100
Registered
2020-07-13
Start date
2020-12-14
Completion date
2027-06-01
Last updated
2026-02-25

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

Conditions

Eating Behavior, Shift Work Type Circadian Rhythm Sleep Disorder

Brief summary

This study will compare eating behaviors and measures of hunger and fullness between day and night workers in order to better understand why night workers are at increased risk for obesity and related diseases.

Interventions

BEHAVIORALPortion size

The amount of food served (g) at the first two meals of each day. These amounts will vary across 4 weeks.

Sponsors

Columbia University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Statistician will be blinded to participant group and condition.

Intervention model description

This is a mixed design with two participant groups (between-subject), day and night workers, each being exposed to 4 levels of food portion size (within-subjects factor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Work \~ 8-hour shifts during day or night on 3 or more consecutive days of the week * 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

* Pregnant or less than 1 year postpartum at time of study * 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

Design outcomes

Primary

MeasureTime frameDescription
Food intake24-hours intake periodFood by weight (g) in response to variations in portion served
Energy intake24-hours intake periodFood by energy (kcal) in response to variations in portion served
Energy density consumed24-hours intake periodEnergy density consumed (kcal/g) in response to variations in portion served

Secondary

MeasureTime frameDescription
Appetite-regulating hormones2-hours measurement periodAppetite-regulating hormones, including Glucagon-like-peptide 1 (GLP-1) and ghrelin will be analyzed from plasma from whole blood samples collected while fasted and at 30, 60, 90, and 120 min postprandial. Area under the curve of plasma concentrations will be calculated for each individual appetite-regulating hormone
Hunger and fullness24-hours measurement periodSubjective measures related to hunger, fullness, and prospective consumption will be measured before and after meals via visual analog scales. The range of scores are 0 mm to 100 mm, with higher scores indicating greater feelings of the corresponding measure (e.g. greater hunger). Post-meal measures, adjusted for the corresponding pre-meal measure, will be analyzed as individual outcomes. Area under the curve will also be calculated for each measure.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORFaris M Zuraikat, PhD

Columbia University

PRINCIPAL_INVESTIGATORMarie-Pierre St-Onge, PhD

Columbia University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026