The Influence of Nocturnal Food Intake in Eating Behavior of Night Workers

Sponsor
Federal University of Uberlandia (Other)
Overall Status
Completed
CT.gov ID
NCT03800732
Collaborator
(none)
10
1
1
18
0.6

Study Details

Study Description

Brief Summary

This study aimed to verify the influence of night work and food intake during the night shift on the eating behavior of fixed night workers the next day.

Condition or Disease Intervention/Treatment Phase
  • Other: With Meal during night work
  • Other: Without Meal during night work
  • Other: Sleep night
N/A

Detailed Description

Night work causes restriction of sleep time and circadian misalignment and, therefore, have been associated with nutritional and metabolic impairments. The objective of the present study is to verify the influence of night work and food intake in this period on the behavior of the following day. The workers selected by criteria and inclusion and exclusion will be evaluated at the baseline: anthropometric parameters, food consumption and perception, duration of food consumption, sleep habits and chronobiological pattern (sleep monitoring by actigraphy, chronotype, social jet lag), parameters biochemical (blood count, lipidogram, C-reactive protein, cortisol, glucose, insulin).Subsequently, 30 workers will integrate a randomized and controlled crossover clinical study with three randomly established interventions: (1) two nights of work without meals during the shift; (2) two nights of work with a meal during the shift; (3) two nights sleep. Participants will go to the laboratory the morning after the second night of each condition to offer a test meal ad libitum, which will consist of foods of various compositions and food groups. Preprandial metabolic assessments will be conducted (ghrelin, GLP-1 - glucagon-like peptide 1, PYY-peptide YY). The following postprandial evaluations will be carried out and in the 24 hours following the experiment: food choices (record of all foods) and food perceptions (hunger, appetite, satiety and eating). It is expected to determine how nocturnal versus nocturnal work, and nocturnal fasting versus nocturnal fasting affect the next day's food choices.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Influence of Nocturnal Food Intake in Eating Behavior of Night Workers: Randomized Cross-over Study.
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Sep 1, 2019
Actual Study Completion Date :
Jul 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Night workers.

Night workers of the military police of Minas Gerais, Uberlândia, who will participate in the three interventions of the study.

Other: With Meal during night work
Two nights of work with a meal during the shift and after will go to the laboratory the morning for eating a test meal ad libitum, which will consist of foods of various compositions and food groups. Preprandial metabolic assessments will be conducted (ghrelin, GLP-1 - glucagon-like peptide 1, PYY-peptide YY). The following postprandial evaluations will be carried out and in the 24 hours following the experiment: food choices (record of all foods) and food perceptions (hunger, appetite, satiety and eating).

Other: Without Meal during night work
Two nights of work without a meal during the shift and after will go to the laboratory the morning for eating a test meal ad libitum, which will consist of foods of various compositions and food groups. Preprandial metabolic assessments will be conducted (ghrelin, GLP-1 - glucagon-like peptide 1, PYY-peptide YY). The following postprandial evaluations will be carried out and in the 24 hours following the experiment: food choices (record of all foods) and food perceptions (hunger, appetite, satiety and eating).

Other: Sleep night
Two sleep nights and after will go to the laboratory the morning for eating a test meal ad libitum, which will consist of foods of various compositions and food groups. Preprandial metabolic assessments will be conducted (ghrelin, GLP-1 - glucagon-like peptide 1, PYY-peptide YY). The following postprandial evaluations will be carried out and in the 24 hours following the experiment: food choices (record of all foods) and food perceptions (hunger, appetite, satiety and eating).

Outcome Measures

Primary Outcome Measures

  1. Preprandial metabolic [6 months]

    Ghrelin, GLP-1 - glucagon-like peptide 1, PYY-peptide YY

  2. Change of food perceptions [6 months]

    To evaluate appetite, satiety and postprandial satisfaction, a visual analogue scale was applied before and after consumption of the proposed meal, with the questions, "How much hunger did you have before the meal?"; "After the meal, how did you feel?"; "How much did you like the meal?", Signaling all responses on a 0 to 10 cm scale.

Secondary Outcome Measures

  1. Food behavior [6 months]

    Record of food consumption of the meals / snacks held following the test meal.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Agree to participate in the study and sign the Informed Consent Form (EHIC).

  • No significant changes in body mass in the last 6 months.

  • With stable food and sleep routine in the last two months.

Exclusion Criteria:
  • Failure to provide the information or material necessary for the development of the study.

  • Report of chronic non-communicable diseases.

  • Report of diagnosed and untreated psychiatric disorders.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cibele Aparecida Crispim Uberlândia Minas Gerais Brazil 38.405-320

Sponsors and Collaborators

  • Federal University of Uberlandia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cibele Aparecida Crispim, Principal investigator, Federal University of Uberlandia
ClinicalTrials.gov Identifier:
NCT03800732
Other Study ID Numbers:
  • 86382218.6.0000.5152
First Posted:
Jan 11, 2019
Last Update Posted:
Feb 14, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2022