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Recruiting NCT06288568

Night Shift Work and Biomarkers of Obesity Risk in Hospital and Industry Workers

Observational Obesity Shift-work Disorder Circadian Rhythm Disorders

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: No intervention.
Who it may be relevant to
Registry conditions: Obesity, Shift-work Disorder, Circadian Rhythm Disorders. Basic parameters: from 21 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
Austria
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

Development and Evaluation of Nutritional Strategies to Reduce and Prevent Obesity in Shiftworkers

Overview

Shift work is a well-known risk factor for the development of overweight and obesity, which may lead to downstream effects such as increased risk of cardiometabolic diseases and cancer. However, the biological and behavioral mechanisms underlying the obesogenicity of night shift work are not well understood. Population-based mechanistic studies in real life shift workers are needed to address how night shift work impacts metabolic health. The investigators aim to characterize the behavioural, environmental, and biological mechanisms and pathways for the association of night shift work and obesity across Europe. The investigators will conduct a cross sectional study in 5 European countries (Austria, Denmark, Germany, Netherlands and Poland) and recruit 1000 rotating night shift workers and day workers (200/country) from the health sector and different industries. Night and day workers will be age-frequency (3 age groups), gender and (where possible) working tasks matched. Participants will complete online questionnaires and report their diet habits in a mobile app. Body composition, dietary behavior and sensory preferences will be tested. Biologic specimens (blood, urine, saliva, hair and feces) will be collected at the workplace on a day where participants are working on a day shift (or a day off). In a subsample (Austria and Netherlands) shift workers will provide biological samples (spot blood, urine and saliva) both on a day shift and on a night shift. Biomarkers including hormones, cellular immunity and inflammation, parameters linked to gut health and metabolism of fat and sugar, appetite, oxidative stress, metabolomics and microbiota will be measured. The investigators hypothesize that compared to day workers, night shift workers will experience disrupted levels of pre-obesity markers. Higher circadian disruption, sleep disruption and mistimed eating patterns workers will be associated with more disrupted biomarker profiles. Among rotating shift workers, night shift will be associated with acute disrupted melatonin production, metabolomic profiles and composition of oral microbiota compared to a day shift.

Interventions

  • Other No intervention
    No intervention

Primary outcome measures

  • high-sensitive C-Reactive Protein (hs-CRP) [Time frame: Baseline]
Secondary outcome measures (12)
  • The investigators will consider levels of hormones in plasma [Time frame: Baseline]
  • The investigators will consider levels of hormones in plasma [Time frame: Baseline]
  • The investigators will consider levels of parameters linked to gut health in serum and in feces [Time frame: Baseline]
  • The investigators will consider levels of parameters linked to gut health in serum and in feces [Time frame: Baseline]
  • The investigators will consider levels of parameters linked to gut health in serum and in feces [Time frame: Baseline]
  • The investigators will consider levels of parameters linked to gut health in serum and in feces [Time frame: Baseline]
  • The investigators will consider parameters of cellular immunity and inflammation in plasma [Time frame: Baseline]
  • The investigators will consider parameters of cellular immunity and inflammation in plasma [Time frame: Baseline]
  • The investigators will consider parameters of cellular immunity and inflammation in plasma [Time frame: Baseline]
  • The investigators will consider parameters of metabolism of fat and sugar in plasma [Time frame: Baseline]
  • The investigators will consider parameters of metabolism of fat and sugar in plasma [Time frame: Baseline]
  • The investigators will consider parameters of metabolism of fat and sugar in plasma [Time frame: Baseline]

Eligibility criteria

Inclusion Criteria shift worker

  • Health care sector or industrial shift worker
  • Employed or self-employed
  • 21 years or older
  • ≥ 24 h/ week
  • Shift work duration > 3 years and currently doing night shifts
  • 4 or more rotating night shifts/month (night shift defined as a work schedule that involves working at least 3 hours between 00:00 and 5:00), at least 2 consecutive nights/month

Inclusion criteria controls

  • Health care sector or industrial work
  • Employed or self-employed
  • 21 years or older
  • ≥ 24 h/ week
  • No night shift or rotating shift work in the last 5 years
  • No history of night shift or rotating shift work for more than 5 years

Exclusion Criteria shift worker and controls:

  • Pregnancy
  • Lactation period
  • BMI of 40 kg/m2 or above
  • Present treatment of a disease e.g. cancer radio- or chemotherapy
  • Chronic diseases if in an ongoing therapy but not after a remission (renal failure, active hepatitis, cirrhosis, myocardial infarction, chronic obstructive pulmonary disease and cancer)
  • Immunodeficiency syndrome, any auto-immune or auto-inflammatory diseases (e.g. type-1 diabetes, multiple sclerosis, lupus, rheumatoid arthritis) and acute episodes of atopic diseases (atopic dermatitis, asthma, type 1 allergies such as hay fever)
  • Bariatric surgery
  • Antibiotics in the last month

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

Austria · 1 center
  • Medical University of Vienna — Vienna

Identifiers

NCT: NCT06288568 · Shift2Health

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗