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Not yet recruiting NCT07394283

Impact of Night Shift Work on Dietary Habits Among Intensive Care and Emergency Healthcare Workers (NUTRINIGHT)

Observational Shift-work Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Healthcare Night Shift Workers.
Who it may be relevant to
Registry conditions: Shift-work Disorder. Basic parameters: 18 years — 64 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Impact of Night Shift Work on Dietary Habits Among Intensive Care and Emergency Healthcare Workers: An Observational Questionnaire-Based Study

Overview

Night shift work is an essential component of healthcare systems, particularly in intensive care units and emergency departments, where continuous patient monitoring and rapid clinical decision-making are required. However, it is associated with diruption of the circadian rhythm , sleep disturbances, and physiological stress, which may influence lifestyle behaviors, including dietary habits. Previous studies have reported that night work can be associated with changes in meal timing, increased caloric intake, preference for energy-dense foods, and reduced overall diet quality.Despite the growing literature on night work and nutrition, data specifically describing dietary habits among healthcare professionals working night shifts in high-intensity clinical settings remain limited. Intensive care units and emergency departments combine high workload, psychological stress, time constraints, and restricted access to appropriate meals during night hours, all of which may affect eating behaviors. Moreover, whether these dietary patterns are specific to healthcare professionals or primarily related to night work itself remains unclear. This observational, cross-sectional study aims to describe dietary habits among healthcare professionals working night shifts in intensive care units and emergency departments, and to compare these habits with those of night workers from non-healthcare sectors. Data will be collected prospectively through a voluntary, anonymous, self-administered online questionnaire during a defined inclusion period. The questionnaire will explore meal timing, eating patterns, food choices, and constraints perceived as influencing dietary behaviors during night work. By providing a descriptive overview of dietary habits across different categories of night workers, the study seeks to improve understanding of how night work and occupational context influence eating behaviors. The findings may contribute to the development of future preventive strategies and workplace health initiatives aimed at improving the health and well-being of night shift workers

Interventions

  • Other Healthcare Night Shift Workers
    Data are collected through an anonymous, self-administered online questionnaire.

Primary outcome measures

  • Dietary Habits of Night Shift Workers [Time frame: At the inclusion]
Secondary outcome measures (3)
  • Meal Timing During Night Shifts [Time frame: At the inclusion]
  • Eating Patterns During Night Shifts [Time frame: At the inclusion]
  • Comparison of Dietary Habits Between Healthcare and Non-Healthcare Night Shift Workers [Time frame: At the inclusion]

Eligibility criteria

Inclusion criteria

  • Adults aged 18 years and older.
  • Currently working night shifts.
  • Employment in healthcare (intensive care units or emergency departments) or in non-healthcare professional sectors
  • Voluntary participation and completion of the online questionnaire

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

France · 1 center
  • CHU de Nice — Nice

Identifiers

NCT: NCT07394283 · 26Onco-Hémato01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗