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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05362279
Other study ID # AAlaca
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 10, 2022
Est. completion date August 10, 2022

Study information

Verified date May 2022
Source Izmir Katip Celebi University
Contact Asli Alaca
Phone +905052741676
Email alaca_asli_1992@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 70
Est. completion date August 10, 2022
Est. primary completion date June 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Training
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.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Izmir Katip Celebi University

References & Publications (1)

Colleti Junior J, Longui TE, Carvalho WB. HIGH-FLOW NASAL CANNULA POST-TRACHEAL EXTUBATION IN A CHILD WITH UPPER AIRWAY OBSTRUCTION: CASE REPORT. Rev Paul Pediatr. 2018 Jul-Sep;36(3):372-375. doi: 10.1590/1984-0462/;2018;36;3;00010. Epub 2018 Jul 10. Portuguese, English. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Knowledge Level - Education Form- Questionnaire To increase the knowledge level of nurses about oxygen therapy with high flow nasal cannula. One month after training
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