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Meal Service for Night Shift Workers
N/A
Recruiting
Research Sponsored by State University of New York at Buffalo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Diagnosis of kidney disease or impairment
Taking medication to lower blood glucose
Timeline
Screening 3 weeks
Treatment Varies
Follow Up two weeks
Summary
This trial is testing if changing the amount of protein and carbohydrates in meals can help control blood sugar levels in night shift EMS workers. The study will monitor participants' blood sugar and activity levels while they follow different meal plans. The goal is to find a diet that helps keep their blood sugar stable during night shifts.
Who is the study for?
This trial is for night shift EMS providers who have been working nights for at least a year and whose main job is patient care. It's not open to those with metabolic diseases like diabetes, pregnant women or those planning pregnancy, people with kidney disease, food allergies/intolerances, digestive disorders, or on blood glucose-lowering meds.
What is being tested?
The study tests how meal services can affect blood sugar control in night shift EMS workers. It will also assess if it's practical to implement such a dietary intervention within this workforce.
What are the potential side effects?
Since the intervention involves meal service without medical treatments or drugs, side effects are minimal but may include potential food-related reactions based on individual tolerances.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been diagnosed with kidney disease.
Select...
I am on medication to control my blood sugar.
Select...
I have been diagnosed with a metabolic disease like diabetes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ four days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~four days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Compliance
Glycemic control
Secondary study objectives
Perceived stress
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: High proteinActive Control1 Intervention
Consuming a meal composed of 2:1 grams of protein to carbohydrate during the night shift between 7pm-7am
Group II: Moderate proteinPlacebo Group1 Intervention
Consuming a meal composed of 1:1 grams of protein to carbohydrate during the night shift between 7pm-7am
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Shift Work Sleep Disorder (SWSD) include pharmacological options like melatonin and melatonin agonists such as tasimelteon, which help regulate the sleep-wake cycle by mimicking the body's natural sleep hormone. Nonpharmacological interventions include light therapy, which adjusts the circadian rhythm through timed exposure to bright light.
Dietary interventions that modulate glycemic control can also play a role by stabilizing blood sugar levels, potentially reducing nighttime awakenings and improving sleep quality. These treatments are essential for SWSD patients as they help align their sleep-wake cycles with their work schedules, enhancing alertness, performance, and overall health.
SHIFTPLAN: a randomized controlled trial investigating the effects of a multimodal shift-work intervention on drivers' fatigue, sleep, health, and performance parameters.Improving fatigue risk management in healthcare: A scoping review of sleep-related/ fatigue-management interventions for nurses and midwives (reprint).Shift work sleep disorder: burden of illness and approaches to management.
SHIFTPLAN: a randomized controlled trial investigating the effects of a multimodal shift-work intervention on drivers' fatigue, sleep, health, and performance parameters.Improving fatigue risk management in healthcare: A scoping review of sleep-related/ fatigue-management interventions for nurses and midwives (reprint).Shift work sleep disorder: burden of illness and approaches to management.
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Who is running the clinical trial?
State University of New York at BuffaloLead Sponsor
268 Previous Clinical Trials
52,290 Total Patients Enrolled
David Hostler, PhDStudy ChairUniversity at Buffalo
1 Previous Clinical Trials
124 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a digestive disorder.I am on medication to control my blood sugar.I have been diagnosed with a metabolic disease like diabetes.I have been diagnosed with kidney disease.
Research Study Groups:
This trial has the following groups:- Group 1: Moderate protein
- Group 2: High protein
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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