Rational Use of Personal Protective Equipment During COVID-19 Pandemic

N/ACompletedNCT04712045

University of Oxford67 enrolled

Overview

This study aims to improve the personal protective equipment (PPE) used while treating patients with COVID-19, to protect staff and avoid cross-infection of patients. Protecting staff from infection during the Covid pandemic is critical to maintaining health services. Mistakes in using protective equipment (PPE) are the commonest avoidable factor in staff becoming infected at work. Recently, intensive care doctors have also reported an increase in the spread of dangerous multi-resistant bacteria between patients, which appears likely to be transmitted between patients by Level 2 PPE worn by staff (specifically gown sleeves). This study therefore seeks to develop and test a new protocol to decrease cross-infection risks whilst using Level 2 PPE.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Covid19 Personal Protective Equipment

Interventions

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. NHS staff and works in the Adult Intensive Care Unit, Neuro Intensive Care Unit or Cardio-thoracic Intensive Care Unit 2. Trained in the correct use of Level 2 PPE according to current guidance 3. Trained in ICU COVID19 Intubation and Proning protocols 4. Willing and able to give informed consent for participation in the study. Exclusion Criteria: 1\. taking any medication which can cause photosensitivity reactions in the preceding 3 months

Outcomes

Primary Outcomes

Proportion of participants and simulated patients with contamination as assessed by ultraviolet light

The primary outcome of this study is the proportion of participants and simulated patients who were contaminated with fluorescent powder as examined under a UV light, using a response of "YES" or "NO", when participants wore new (experimental) Level 2 PPE in comparison to the standard (control) Level 2 PPE

Time frame: immediately after simulations

Secondary Outcomes

Participants' perception of personal comfort and safety and safety of the patients as assessed through structured questionnaire

We will measure the participants' perception of personal comfort and safety and the safety of the patient when wearing experimental versus control Level 2 PPE, during simulation tasks, using a 10 point Likert scale response to a structured questionnaire

Time frame: immediately before simulations and immediately after simulations

changes in participants perception of personal comfort and safety and safety of patients as assessed through a semi-structured questionnaire

We will measure changes in participants perception of their personal comfort and safety and the safety of patients when wearing each type of PPE using a semi-structured interview (a) before the PPE training, (b) after the PPE training, and (c) after the simulation training exercises.

Time frame: immediately before training, immediately after training and immediately after simulation

The difference in the area of contamination between New and Standard PPE as analyzed through python script

we will perform a quantitative analysis of the area of contamination of participants and simulated patients and assess the difference between when participants wore new (experimental) Level 2 PPE and the standard (control) Level 2 PPE, using pre-coded functions with python script.