MedPath

Eating Behaviors in Shift Workers

Not Applicable
Active, not recruiting
Conditions
Eating Behavior
Shift Work Type Circadian Rhythm Sleep Disorder
Interventions
Behavioral: Portion size
Registration Number
NCT04468672
Lead Sponsor
Columbia University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
100
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Day workerPortion sizeMen and women who work only day shift for at least 3 consecutive days of the week
Night workerPortion sizeMen and women who work only night shift for at least 3 consecutive days of the week
Primary Outcome Measures
NameTimeMethod
Food intake24-hours intake period

Food by weight (g) in response to variations in portion served

Energy intake24-hours intake period

Food by energy (kcal) in response to variations in portion served

Energy density consumed24-hours intake period

Energy density consumed (kcal/g) in response to variations in portion served

Secondary Outcome Measures
NameTimeMethod
Appetite-regulating hormones2-hours measurement period

Appetite-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 period

Subjective 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.

Trial Locations

Locations (1)

Columbia University Irving Medical Center

🇺🇸

New York, New York, United States

© Copyright 2025. All Rights Reserved by MedPath