Manual Ventilation Efficacy With MVG Device

N/ACompletedNCT05059366

University of Miami32 enrolled

Overview

The purpose of this research is to investigate the efficacy of the newly designed ventilation grip device (MVG device).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Ventilator Lung

Interventions

Manual Ventilation Grip DeviceDEVICE

Manual Ventilation Grip Device is an add-on device placed on a standard valve mask to assist ventilation.

2VEOTHER

the standard 2VE technique for ventilation

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1\. Current medical students, Post Graduate Year 1 (PGY1) residents or residents from other specialties with no prior experience in hand mask ventilation techniques or anesthesiology residents and attendings with at least 2 or more years of clinical experience Exclusion Criteria: 1. Refusal to participate in the study. 2. Medical students with prior experience in hand mask ventilation techniques (i.e. experiences in previous careers such as nursing or Emergency Medical Technician (EMT) professions) 3. Any physical inability to adequately perform ventilation

Locations (1)

University of Miami

Miami, Florida, United States

Outcomes

Primary Outcomes

Tidal Volume

As measured using the ventilator machine in milliliters

Time frame: Day 1

Secondary Outcomes

Fatigue as Measured by NASA-TLX Questionnaire

NASA Task Load Index (TLX) questionnaire has a total overall workload score ranging from 0 and 126 with the higher score indicating greater demand.

Time frame: Day 1

Fatigue as Measured by SOFI Questionnaire

Swedish Occupational Fatigue Inventory (SOFI) questionnaire has a total score ranging from 0 to 120 with the higher score indicating greater fatigue

Time frame: Day 1

Data from ClinicalTrials.gov

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