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EMS Providers' Health Initiative Study

EMS Providers' Health Initiative Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05153759
Enrollment
40
Registered
2021-12-10
Start date
2022-06-07
Completion date
2026-12-01
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shift-work Disorder

Keywords

EMS, Night shift, Nutrition, Insulin resistance, Circadian rhythm

Brief summary

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.

Detailed description

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.

Interventions

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

Sponsors

State University of New York at Buffalo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Glycemic controlTwo weeksDaily mean blood glucose
ComplianceFour daysPercent of participants who adhere to the dietary intervention

Secondary

MeasureTime frameDescription
Perceived stressTwo weeksDaily rating of stress on a scale of one to 10 where 10 is the most stressed the participant has ever been

Countries

United States

Contacts

CONTACTTegan H Mansouri, PhD
teganman@buffalo.edu716-829-5596
CONTACTJocelyn Stooks, MS
jstooks@buffalo.edu716-829-5596
STUDY_CHAIRDavid Hostler, PhD

University at Buffalo

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026