Clinical trial Recruiting at 1 site Interventional Ages 20 to 40

Examining blood vessel function and oxidative stress in EMTs

Official title: Vascular Function and Oxidative Stress in Emergency Medical Responders

Run by University of Delaware · NCT06985394 · Data updated 2026-11-12

This study tests if overnight shifts affect blood vessel health in EMTs and whether taking antioxidant supplements can help reduce any negative effects.

Quick facts

Study typeInterventional
Ages20 Years to 40 Years
SexAll
Enrollment45 (estimated)
SponsorUniversity of Delaware
Academic / other
Locations1 site (Newark, Delaware)
StatusRecruiting
StartedMay 14, 2025
Main results expectedSeptember 2025
Study endsOctober 2025
Registry record updatedMay 22, 2025
Trial IDNCT06985394 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are active EMTs who have been working night shifts for at least one year and meet specific health criteria.

Probably not a fit

Patients with chronic diseases or sleep disorders, or those taking sleep aids, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to investigate the effects of overnight shift work on blood vessel function and oxidative stress in emergency medical technicians (EMTs). Participants will report to the lab after working overnight shifts to assess their vascular health and oxidative stress levels. They will also receive either an antioxidant supplement or a placebo during their shifts to determine if antioxidants can mitigate the negative impacts of night work. The study seeks to provide insights into how shift work affects EMTs' cardiovascular health and whether dietary interventions can help.

Why it matters

Potential benefit: If successful, this study could lead to improved health outcomes for EMTs by identifying effective strategies to counteract the negative effects of night shift work.

How similar studies have gone: While there is existing research on the health impacts of shift work, this specific approach of using antioxidants in EMTs is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Body mass index between 18.5 and \<35 kg/m²
* Seated resting systolic blood pressure \< 140 mmHg, and seated resting diastolic blood pressure \< 90 mmHg
* Participant must be an active first responder that works shift work schedules. e.g., emergency medical responders, basic life support emergency medical technicians (i.e., BLS EMT), advanced life support emergency medical technicians (A-EMT), and paramedics
* Participant must have been working shift work for at least 1 year
* Participant must work at least 4 night shifts per month

Exclusion Criteria:

* Participant is unwilling or unable to give consent
* Participant has been diagnosed with any chronic disease (a history of high blood pressure, heart disease, diabetes, cancer, kidney disease)
* Participant has been diagnosed with a sleep disorder (e.g., insomnia, restless leg syndrome, sleep apnea)
* Participant is currently taking melatonin or other sleep aids (e.g., Ambien, sedatives, etc.), or any supplements/medications known to alter sleep patterns. Participants using melatonin must undergo a minimum 72-hour washout period prior to study participation to ensure baseline sleep patterns are not affected\[15, 16\]
* Resting blood pressure \>140/90 mmHg
* Body mass index \<18.5 or \>35 kg/m2
* Currently pregnant or breast feeding (women only)
* Currently use tobacco or nicotine products (≥1 cigarette, cigar, e-cigarette, vape, or any other nicotine-containing product in the last month), including smokeless tobacco (e.g., chewing tobacco, snuff, dip, snus), nicotine lozenges or gum, heated tobacco products, and any illicit drugs

Where it's running

  • University of Delaware
    Newark, Delaware, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.