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NCT Number: NCT06550115

Impact of Circulating and Tissue-specific Lipids on Vascular Function and Insulin Sensitivity in Chronic Night Shift Workers

People who experience repeated bouts of circadian misalignment, such as shift workers, are at higher risk of cardiovascular disease (CVD) and Type 2 diabetes (T2D) compared to daytime workers. However, the mechanism(s) by which shift work and associated circadian misalignment increase CVD and T2D risk are unknown. This project will examine whether elevated plasma lipids are a mechanism by which circadian misalignment impairs vascular function, insulin sensitivity, glucose homeostasis and muscle lipid accumulation, which could be targeted to prevent and treat cardiometabolic disease in people who chronically experience circadian misalignment, which includes more than 20% of the US workforce.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Colorado State University

Fort Collins, Colorado, 80523, United States

Location status: Recruiting

Location contact

Ellen Lyon, MS

CONTACT

[email protected]

970-491-3103

Josiane L Broussard, PhD

PRINCIPAL_INVESTIGATOR

About this study

There is growing recognition that timing of behaviors, such as eating, sleeping, and activity, have a significant impact on human health and disease risk. For example, when people are awake at the "wrong" time of the day (i.e. during the biological night), a mismatch occurs between behavior and biology, termed circadian misalignment. Shift workers experience repeated bouts of circadian misalignment and are at higher risk of cardiovascular disease (CVD) and Type 2 diabetes (T2D) compared to people who work days. However, the mechanism(s) by which shift work and associated circadian misalignment increase CVD and T2D risk are unknown.

Data from the investigators and others demonstrate impaired vascular endothelial function and insulin sensitivity during circadian misalignment, two important risk factors for future development of CVD and T2D. Furthermore, the investigators published and unpublished data support that circadian misalignment increases circulating bioactive lipids known to associate with impaired endothelial function and insulin resistance. Indeed, shift workers also have elevated circulating lipids, though it is not known which specific lipids are elevated, and whether they are associated with impaired vascular function and/or insulin sensitivity. Using a circadian-based eating intervention (time-restricted eating; TRE), we can consistently reduce lipids in circulation, as well as reduce heart rate and blood pressure and improve glucose homeostasis.

Therefore, the overall objective for this project is to examine whether increased plasma lipids are a potential mechanism by which chronic circadian misalignment impairs cardiovascular and metabolic health with the long-term goal of identifying novel therapeutic targets to combat the risks for disease when circadian misalignment is unavoidable. The central hypothesis is that reducing plasma lipids in night shift workers via TRE will improve vascular function, insulin sensitivity and glucose homeostasis, and reduce muscle tissue lipid accumulation. To test the hypothesis, we will conduct a 12-week randomized crossover study in 50 non-rotating night shift workers (25Females/25Males; 18-65years) with existing cardiometabolic risk factors. At the end of each 4-week outpatient condition (TRE vs Control with an intervening 4-week washout period), we will conduct rigorous 3-day inpatient assessment to determine the impact of plasma lipid reduction via TRE in chronic night shift workers on 1) vascular function and blood pressure; and 2) whole body and muscle-specific insulin sensitivity, glucose homeostasis and muscle lipid accumulation.

Achievement of these aims will identify a potential mechanism by which circadian misalignment impairs vascular function and insulin sensitivity (elevated plasma lipids), as well as a non-pharmacological tool (TRE) that could be implemented to reduce cardiometabolic disease risk in populations at elevated risk, in 20% of the US workforce who work nonstandard hours including military personnel, police, paramedics, firefighters, pilots, medical doctors and nurses, as well as people with sleep and circadian disorders.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-65 years old
  • worked the night shift for the last 1 year or more,
  • habitually sleep 5-9 hours per 24h period (night shift workers typically experience chronic insufficient sleep),
  • body mass index (BMI) of 20.0 - 35.0 kg/m2 and weight stable (plus or minus 5% of current body weight in the last 6 months); sedentary to mild physical activity level (less than 2 days of planned exercise per week);

Exclusion criteria

  • existing diagnosed sleep or eating disorder (e.g. obstructive sleep apnea [OSA], periodic limb movements of sleep [PLMS], narcolepsy, travel more than 1 time zone in 3 weeks before the study; anorexia nervosa, more than one food allergy to maintain flexibility in diet planning);
  • following any TRE (time-restricted eating) or intermittent fasting plan in the last year;
  • following any special diet plan, like paleo, keto, gluten-free or vegan, that can affect the primary lipid outcome measures in the last 6 months; any clinically significant surgical condition within the last year;
  • diagnosed diabetes or cardiovascular disease
  • The prevalence of insomnia in shift workers is fairly high, ranging from 12.8% to 76.4%, which is higher than estimated for the general population. Insomnia itself is associated with elevated neural cardiovascular responsiveness to stress compared to people without insomnia. Thus, since excessive sleepiness and symptoms of insomnia may be present in night shift workers they will not be exclusionary.

Treatment and study plan

Time-restricted eating

Behavioral

Night shift workers will participate in 4 weeks of fasting during the biological nighttime while remaining awake during overnight work shifts.

Other names: Time-restricted feeding, TRF, TRE

Control eating

Behavioral

Night shift workers will participate in 4 weeks of Control eating across the daytime and nighttime hours while remaining awake during overnight work shifts.

Primary outcomes

  1. Blood pressure via 24-hour assessments

    Time frame: Collected during inpatient laboratory visit after 4 weeks of Control and TRE

    Four weeks of TRE during shift work will reduce 24-hour blood pressure versus Control.

  2. Insulin sensitivity via clamp

    Time frame: Collected during inpatient laboratory visit after 4 weeks of Control and TRE

    Four weeks of TRE during shift work will improve insulin sensitivity versus Control.

Secondary outcomes

  1. Cerebrovascular reactivity via transcranial doppler

    Time frame: Collected during inpatient laboratory visit after 4 weeks of Control and TRE

    Four weeks of TRE during shift work will improve cerebrovascular reactvity versus Control.

  2. Muscle lipid accumulation via lipidomics

    Time frame: Collected during inpatient laboratory visit after 4 weeks of Control and TRE

    Four weeks of TRE during shift work will reduce muscle lipid accumulation versus Control.

Other outcomes

  1. 24-hour blood sampling for lipids, glucose, insulin, and vascular markers

    Time frame: Collected during inpatient laboratory visit after 4 weeks of Control and TRE

    Four weeks of TRE during shift work will improve 24-hour markers of vascular function versus Control.

Study contacts

Contact information is provided by the study sponsor or research team.

Ellen Lyon, MS

CONTACT

[email protected]

9704913103

Josiane L Broussard, PhD

CONTACT

[email protected]

9704913103

Sponsors and collaborators

Lead sponsor

Colorado State University

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • University of Colorado, Denver

Registry information

Acronym: SHINE

Important dates

Study start
2024
Primary completion
2028
Study completion
2029
First posted
Aug 12, 2024
Registry last updated
Dec 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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