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Clinical Trials/NCT05362279
NCT05362279UnknownNot Applicable

The Effect of Training on Oxygen Therapy With High Flow Nasal Cannula on the Knowledge Level of Pediatric Nurses; A Randomized Controlled Trial

Izmir Katip Celebi University0 sites70 target enrollmentStarted: May 10, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
70
Primary Endpoint
Knowledge Level - Education Form- Questionnaire

Study Overview

Brief Summary

This study was conducted to evaluate the oxygen therapy methods used in pediatric services and to specify the roles and responsibilities of nurses in the application of HFNC, which is one of these methods. Although the decision to implement this treatment method is under the responsibility of the physician in Turkey, the use of the device, observing the effectiveness of the treatment, monitoring and recording the changes in the vital signs of the children are under the responsibility of the nurses shows the importance of the nursing perspective on HFNC.

Detailed Description

High-flow nasal cannula oxygen therapy (HFNC) which meets the patient's ventilation need is a non-invasive ventilation system in which warmed and humidified oxygen is administered to the patient at varying flows with the help of a nasal cannula.This study will be conducted as a randomized controlled study with the participation of 70 nurses working in the pediatric clinics of a public hospital between December 2021 and May 2022, as an experimental group (n=35) and a control group (n=35). In the study, two-stage sampling method will be used to determine the nurses who will take place in the experimental and control groups. After the nurses are stratified according to their professional years, assignment to the experimental and control groups will be made by simple random sampling method. The experimental group will be given a pre-test before the training and a post-test one month after the training. In order to avoid interaction between the two groups, the data of the nurses in the control group will be collected first. The knowledge level of the nurses in the experimental and control groups will be evaluated with the HFNC Information Form.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Nurses working in any of the pediatric emergency departments, pediatric clinics
  • No previous training in HFNC treatment
  • Follow-up of patients treated with HFNC
  • Volunteering to participate in research

Exclusion Criteria

  • Those who have received in-service training on HFNC implementation
  • Those who work as responsible nurses or training nurses in the clinics where the research will be conducted

Outcomes

Primary Outcomes

Knowledge Level - Education Form- Questionnaire

Time Frame: One month after training

To increase the knowledge level of nurses about oxygen therapy with high flow nasal cannula.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Izmir Katip Celebi University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aslı Alaca

Principal Investigator

Izmir Katip Celebi University

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