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Portion Size for Shift Work Sleep Disorder

N/A
Recruiting
Led By Faris M Zuraikat, PhD
Research Sponsored by Columbia University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 20-55 years of age
Metabolically healthy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24-hours intake period
Awards & highlights

Study Summary

This trial will look at whether different eating behaviors during the day or night impact feelings of hunger and fullness in people who work night shifts.

Who is the study for?
This trial is for day or night shift workers aged 20-55, with a BMI of 19-35, living in the NYC area. They must be metabolically healthy and weight stable for the past three months. It's not open to pregnant women, smokers, those with certain health conditions like cardiovascular disease or diabetes, or anyone on a recent diet program.Check my eligibility
What is being tested?
The study is looking at how portion size affects hunger and fullness in day versus night shift workers to understand their higher obesity risk. Participants' eating behaviors will be compared based on their work shifts.See study design
What are the potential side effects?
Since this trial involves monitoring eating behavior rather than testing a drug or medical treatment, there are no direct side effects associated with participating in this study.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 20 and 55 years old.
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My metabolism is healthy.
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I work at least 8 hours a day for 3 or more days each week.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24-hours intake period
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24-hours intake period for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Energy density consumed
Energy intake
Food intake
Secondary outcome measures
Appetite-regulating hormones
Hunger and fullness

Trial Design

2Treatment groups
Active Control
Group I: Day workerActive Control1 Intervention
Men and women who work only day shift for at least 3 consecutive days of the week
Group II: Night workerActive Control1 Intervention
Men and women who work only night shift for at least 3 consecutive days of the week

Find a Location

Who is running the clinical trial?

Columbia UniversityLead Sponsor
1,426 Previous Clinical Trials
2,473,708 Total Patients Enrolled
1 Trials studying Eating Disorders
202 Patients Enrolled for Eating Disorders
Faris M Zuraikat, PhDPrincipal InvestigatorColumbia University
Marie-Pierre St-Onge, PhDPrincipal Investigator - Columbia University
Columbia University
8 Previous Clinical Trials
341 Total Patients Enrolled

Media Library

Day worker Clinical Trial Eligibility Overview. Trial Name: NCT04468672 — N/A
Eating Disorders Research Study Groups: Day worker, Night worker
Eating Disorders Clinical Trial 2023: Day worker Highlights & Side Effects. Trial Name: NCT04468672 — N/A
Day worker 2023 Treatment Timeline for Medical Study. Trial Name: NCT04468672 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~19 spots leftby Jan 2025