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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-10

Study Completion Date

2022-08-10

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Pediatric

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized controlled study with pretest-posttest experimental and control groups

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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Test after post-test training

Pre-test will be applied to the nurses in the experimental group before the training. The post-test will be applied to the experimental group, to which the pre-test was applied, one month after the training was given.

Group Type EXPERIMENTAL

Training

Intervention Type OTHER

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.

Test without training

The nurses in the control group are the group to be administered the post-test without any intervention after the pre-test. The post-test will be administered one month after the pre-test.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes