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The Effect of Education on Nurses' Knowledge About High-flow Nasal Cannula Oxygen Therapy

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05362279
Enrollment
70
Registered
2022-05-05
Start date
2022-05-10
Completion date
2022-08-10
Last updated
2022-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric

Keywords

HFNC, Nursing Care, Knowledge Level, Education

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.

Interventions

OTHERTraining

One month after the pre-test, the post-test will be administered to the nurses who will be in the control group. Nurses who will be in the experimental group will be given training after the pre-test. A post-test will be administered one month after the training.

Sponsors

Izmir Katip Celebi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

Randomized controlled study with pretest-posttest experimental and control groups

Eligibility

Sex/Gender
ALL
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

Design outcomes

Primary

MeasureTime frameDescription
Knowledge Level - Education Form- QuestionnaireOne month after trainingTo increase the knowledge level of nurses about oxygen therapy with high flow nasal cannula.

Contacts

Primary ContactAslı Alaca
alaca_asli_1992@hotmail.com+905052741676

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026