Impact of Extracorporeal Membrane Oxygenation Care Strategy Application Development

March 22, 2024 updated by: Pei-Hung Liao

National Taipei University of Nursing and Health Science

The objective of this study was to develop an educational training App for ECMO care, and to apply a blended learning approach to improve the knowledge and skills of nurses.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

In recent years, for patients with acute cardiac infarction, severe cardiac shock, and refractory acute respiratory distress syndrome, the intervention of Extracorporeal Membrane Oxygenation (ECMO) has become an adjunctive treatment for severe cardiopulmonary diseases, which can temporarily replace cardiopulmonary function, slow the deterioration of cardiopulmonary function, and buy time to assist in clinical treatment. However, the education and training of ECMO is mainly based on traditional classroom teaching, which has also been affected by COVID-2019, resulting in training process difficulties as nurses are easily restricted by time and environment.

Study Type

Observational

Enrollment (Estimated)

120

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan
        • National Taipei University of Nursing and Health Science

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

There was a total of 97 participants in this study, with an average of 9 years of nursing experience; the shortest experience was 1 year, and the longest was 29 years, of which 35 (36%) participants were nurses with less than 5 years of experience, and 36 (37%) were nurses with more than 10 years of experience.

Description

Inclusion Criteria:

  • licensed nurse practitioners working in the intensive care center of the teaching hospital and willing to participate in the study.

Exclusion Criteria:

  • those who did not use smart phones.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of knowledge and skills of nurses between groups after the intervention For 6 months.
Time Frame: 6 months
The instruments of this study included a questionnaire survey, the development of the ECMO Care Strategy App, and a blended learning design. The questionnaire survey consisted of three parts: the first part was the basic attributes, the second part was the perception of the ECMO knowledge and care behaviors, and the third part was the ECMO Care Strategy App System Usability Assessment Scale. The questionnaire content was based on the ECMO training literature and digital learning of Rouleau et al. (2019), Thomas et al. (2019), Chaves et al. (2019), Jiritano et al. (2020), as well as the content of the in-hospital ECMO education and training manual, including the care knowledge and perception of care behaviors, for a total of 18 questions.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Pei-Hung Liao, PH.D., National Taipei University of Nursing and Health Science

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2023

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

March 13, 2024

First Submitted That Met QC Criteria

March 22, 2024

First Posted (Actual)

March 26, 2024

Study Record Updates

Last Update Posted (Actual)

March 26, 2024

Last Update Submitted That Met QC Criteria

March 22, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 111-085-B

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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