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The Effect of ECG Rhythm Virtual Interventions to ECG Interpretation and Competence

22. Mai 2026 aktualisiert von: Meri Matala-aho, Tampere University

The Effect of ECG Rhythm Virtual Interventions to ECG Interpretation and Competence in Finnish University Hospitals

The aim of this study is to develop, implement, and evaluate the effects of a virtual ECG rhythm intervention on the interpretation and competence of cardiology nurses in Finnish university hospitals. The virtual ECG rhythm intervention consists of a virtual animation component and a virtual simulation component, both incorporating cardiological patient cases with corresponding ECG rhythms. The virtual animation includes educational content on a total of 31 different ECG rhythms, as well as a virtual simulation containing 6-8 different cardiological patient cases with ECG rhythms (covering 11 distinct rhythms).

The study employs a quasi-experimental design. Cardiology nurses are divided into two groups based on hospital: an intervention group and a control group.

In this study, data will first be collected for the virtual animation component during 2026-2027, followed by data collection for the virtual simulation component during 2027-2028. A baseline measurement of ECG interpretation and competence will be conducted for both groups (n = 508) using an online survey (LimeSurvey) prior to the intervention.

The same measurement schedule will be applied to the virtual simulation component during the 2027-2028 data collection period.

In this study, three (3) reminder letters will be sent at weekly intervals to encourage participation in the study, its surveys, and the virtual interventions. These reminder messages will be distributed via email by unit managers or equivalent personnel in each hospital to the participants.

The virtual intervention will be delivered online via a web service (GitHub) link. Research data on ECG interpretation and competence will be collected using an ECG interpretation measurement instrument administered through an electronic survey (LimeSurvey).

The ECG interpretation instrument was previously developed by the researcher and includes ECG recordings from real patient cases, for which prior permission has been obtained in accordance with the practices of a cardiac care unit in a central hospital. The instrument has been partially updated in terms of ECG rhythms, with additional new ECG recordings included. Permission for the new ECG recordings was obtained in April 2023 from a Finnish wellbeing services county. The instrument also includes ECG recordings from a simulation monitor display.

The ECG interpretation instrument begins with 14 background questions. It includes five questions assessing ECG competence and currently contains 31 ECG interpretation questions, compared to the previous 21 items. Additionally, the end of the instrument includes seven questions assessing the experiences of participants in the intervention group regarding the virtual intervention.

These implementation methods aim to control for the potential influence of external variables, as the intervention and survey are identical for all participants. This consistency could not be guaranteed if the virtual ECG interpretation intervention were delivered, for example, as a traditional theory-based lecture.

The results of the study will be analyzed using statistical methods. The findings can be utilized, for example, in the development of ECG rhythm interpretation and competence training programs for cardiology nurses.

Studienübersicht

Status

Noch keine Rekrutierung

Detaillierte Beschreibung

During the 2026-2027 data collection phase, participants in the intervention group (n = 254) will use the virtual ECG rhythm animation intervention for one month. The experiences of cardiology nurses regarding the virtual ECG rhythm intervention will be collected during the intervention through open-ended questions.

A second measurement of ECG interpretation and competence will be conducted immediately after the intervention (one month after the baseline) for both groups: the intervention group (n = 254) and the control group (n = 254). A third measurement will be conducted three months after the intervention, again for both groups.

Studientyp

Interventionell

Einschreibung (Geschätzt)

508

Phase

  • Unzutreffend

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  • cardiology nurses

Exclusion Criteria:

  • doctors

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Versorgungsforschung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Aktiver Komparator: Intervention group
Data will first be collected for the virtual animation component during 2026-2027, followed by data collection for the virtual simulation component during 2027-2028. A baseline measurement of ECG interpretation and competence will be conducted for both groups (n = 508) using an online survey (LimeSurvey) prior to the intervention. During the 2026-2027 data collection phase, participants in the intervention group (n = 254) will use the virtual ECG rhythm animation intervention for one month. The experiences of cardiology nurses regarding the virtual ECG rhythm intervention will be collected during the intervention through open-ended questions. A second measurement of ECG interpretation and competence will be conducted immediately after the intervention (one month after the baseline) for both groups. A third measurement will be conducted three months after the intervention, again for both groups. The same measurement schedule will be applied to the virtual simulation component.

In this study, data will first be collected for the virtual animation component during 2026-2027, followed by data collection for the virtual simulation component during 2027-2028. A baseline measurement of ECG interpretation and competence will be conducted for both groups (n = 508) using an online survey (LimeSurvey) prior to the intervention.

During the 2026-2027 data collection phase, participants in the intervention group (n = 254) will use the virtual ECG rhythm animation intervention for one month. The experiences of cardiology nurses regarding the virtual ECG rhythm intervention will be collected during the intervention through open-ended questions.

A second measurement of ECG interpretation and competence will be conducted immediately after the intervention (one month after the baseline) for both groups: the intervention group (n = 254) and the control group (n = 254). A third measurement will be conducted three months after the intervention, again for both groups.

Kein Eingriff: Control group
A baseline measurement of ECG interpretation and competence will be conducted for both groups (n = 508) using an online survey (LimeSurvey). A second measurement of ECG interpretation and competence will be conducted immediately after the intervention (one month after the baseline) for both groups. And final, third measurement will be conducted three months after the intervention, again for both groups. The respondents in the control group will continue with standard practice while intervention, meaning that they will not receive any educational material related to ECG interpretation and competence. Instead, learning ECG rhythms will rely on their usual learning processes, such as workplace-based learning.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
ECG Interpretation skills
Zeitfenster: from the start of the intervention until its completion, for a period of three months
Questionnaire (ECG interpretation Scale) is used to assess ECG interpretation skills and expertise
from the start of the intervention until its completion, for a period of three months
ECG Interpretation Scale
Zeitfenster: From participation to the end of the intervention (3 months)

The ECG interpretation instrument begins with 14 background questions. It includes five questions assessing ECG competence and currently contains 31 ECG interpretation questions.

Answers on the ECG interpretation section are scored such that a correct answer earns one point and an incorrect answer earns zero points. The maximum score on the questionnaire is 31, indicating a very high level of proficiency in ECG interpretation.

From participation to the end of the intervention (3 months)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. August 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2028

Studienabschluss (Geschätzt)

31. Dezember 2028

Studienanmeldedaten

Zuerst eingereicht

13. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

22. Mai 2026

Zuerst gepostet (Tatsächlich)

29. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

22. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • 38/2026

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

This study does not collect patient-specific data.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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