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Recruiting

NCT Number: NCT05153759

EMS Providers' Health Initiative Study

This study aims to explore dietary factors that influence glycemic control in night shift EMS providers and to test the feasibility of a dietary intervention among these providers.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University at Buffalo

Buffalo, New York, 14214, United States

Location status: Recruiting

Location contact

David Hostler, PhD

CONTACT

[email protected]

716-829-6795

Tegan Mansouri, PhD

PRINCIPAL_INVESTIGATOR

About this study

This study can be broken down into two phases. Both phases will take place over the course of 3 weeks. During the first week, participants will be scheduled for a single 60-90 minute zoom appointment. During this appointment, informed consent will be obtained, participants will provide health and demographic information, complete several questionnaires, and be familiarized with study protocols. The following week, participants will wear a continuous glucose monitor, actigraph activity monitor, document everything they have to eat and drink, and rate their daily stress levels. Participants will continue this during the final week and will be randomized to consume either a 2:1 or 1:1 protein to carbohydrate ratio during the night shift during this week.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Emergency medical service (EMS) provider
  • Works night shift only for at least one year
  • Provides patient care as primary duty

Exclusion criteria

  • Diagnosis of a metabolic disease (i.e. diabetes, prediabetes, metabolic syndrome)
  • Taking medication to lower blood glucose
  • Pregnant or planning to become pregnant
  • Diagnosis of kidney disease or impairment
  • Allergies or intolerances to study foods
  • Digestive disorder

Treatment and study plan

Meal service

Other

The primary goal is to pilot the feasibility of a meal service intervention in night shift workers

Primary outcomes

  1. Glycemic control

    Time frame: Two weeks

    Daily mean blood glucose

  2. Compliance

    Time frame: Four days

    Percent of participants who adhere to the dietary intervention

Secondary outcomes

  1. Perceived stress

    Time frame: Two weeks

    Daily rating of stress on a scale of one to 10 where 10 is the most stressed the participant has ever been

Study contacts

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

Jocelyn Stooks, MS

CONTACT

[email protected]

716-829-5596

Tegan H Mansouri, PhD

CONTACT

[email protected]

716-829-5596

Sponsors and collaborators

Lead sponsor

State University of New York at Buffalo

Other

Registry information

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Dec 10, 2021
Registry last updated
Jan 27, 2026

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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