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NCT05641194 · ClinicalTrials.gov registry record · NA

EaseAlert: Tactile Firefighter Alerting System

A NA study of Sleep and Heart Rate, sponsored by Embry-Riddle Aeronautical University.

Completed
Registry status
NA
Development phase
47
Enrollment target
2
Study locations

NCT05641194 is a NA study of Sleep and Heart Rate that has completed, run by Embry-Riddle Aeronautical University. The registered enrollment target is 47 participants, below the 4,166-participant average among 151 other Sleep trials with a reported enrollment target (99% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT05641194, a NA study of Sleep and Heart Rate, has completed, sponsored by Embry-Riddle Aeronautical University.

COMPLETED
Registry status
NA
Development phase
47 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this research is to test a commercially viable Fire Fighter Altering System (FFAS) comprised of proprietary wearables and optional bed shakers called BunkAlerts; collectively "personal alerting devices" as an alternative approach to the traditional fire alarm system used in fire stations. Participants (fire fighters) will be asked to take part in the study to investigate the impact of the new FFAS on cardiovascular response and sleep. This study includes three phases: 1) baseline, 2) implementation of EaseAlert FFAS with traditional alarm, and 3) implementation of EaseAlert FFAS without traditional alarm. Participants will be asked to wear an Actigraph wGT3x-BT and Polar H10 device to record sleep and heart rate data for 12 days at work in addition to EaseAlert FFAS device for 8 out of the 12 days at work. They will also be asked to complete a questionnaire and complete daily journal entries.

Interventions

  • DEVICE Legacy Alerting System
  • DEVICE Intervention 2: EaseAlert Standalone

Study Locations (2)

Missouri

  • Central Jackson County Fire District - Blue Springs

Oklahoma

  • Stillwater Fire Department - Stillwater

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2023-08-26
Est. Completion 2025-01-31
Phase NA

What the Registry Record Tells You About NCT05641194

The ClinicalTrials.gov registry entry for NCT05641194 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,166-participant average among 151 other Sleep trials with a reported enrollment target (99% lower). The listed sponsor is Embry-Riddle Aeronautical University, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Sleep appearing as the primary indexed condition, and to 2 interventions - of which Legacy Alerting System is the first listed.

NCT05641194 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Missouri, Oklahoma.

Frequently Asked Questions

What is clinical trial NCT05641194 about?

NCT05641194 is a clinical study titled "EaseAlert: Tactile Firefighter Alerting System". The purpose of this research is to test a commercially viable Fire Fighter Altering System (FFAS) comprised of proprietary wearables and optional bed shakers called BunkAlerts; collectively "personal alerting devices" as an alternative approach to the traditional fire alarm system used in fire stati...

What is the current status of trial NCT05641194?

This trial is currently completed. It is a NA study. The enrollment target is 47 participants. The study started on 2023-08-26. Estimated completion is 2025-01-31.

What conditions does trial NCT05641194 study?

This clinical trial studies the following conditions: Sleep, Heart Rate, Sleep Habit.

What interventions are being tested in trial NCT05641194?

The interventions under investigation include: Legacy Alerting System (DEVICE), Intervention 2: EaseAlert Standalone (DEVICE).

Who is sponsoring clinical trial NCT05641194?

This trial is sponsored by Embry-Riddle Aeronautical University, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05641194 being conducted?

This trial has 2 study locations across Missouri, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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