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Effects of Two Teaching Methods on Nursing Students' Attitudes Toward Medical Errors

12. september 2026 oppdatert av: Saglik Bilimleri Universitesi

The Effect of Patient Safety Education Delivered Through Two Different Teaching Methods on Nursing Students' Attitudes Toward Medical Errors: A Randomized Controlled Trial

The aim of this study is to compare the effects of patient safety education delivered through the Pecha Kucha method, scenario-based teaching, and traditional teaching on nursing students' attitudes toward medical errors. Research Hypotheses: H1: Patient safety education delivered through the Pecha Kucha method significantly improves nursing students' attitudes toward medical errors. H2: Scenario-based patient safety education significantly improves nursing students' attitudes toward medical errors. H3: Nursing students who receive patient safety education through the Pecha Kucha method demonstrate significantly greater improvement in their attitudes toward medical errors than those in the control group. H4: Nursing students who receive scenario-based patient safety education demonstrate significantly greater improvement in their attitudes toward medical errors than those in the control group. H5: There is a significant difference between the Pecha Kucha method and scenario-based teaching in terms of changes in nursing students' attitudes toward medical errors. This study is designed as a three-arm, parallel-group, randomized controlled trial with a pretest-posttest design to evaluate the effects of two different teaching methods for patient safety education on nursing students' attitudes toward medical errors. Participants will be randomly assigned to one of the following three groups: Group 1 (Pecha Kucha Group): Participants will receive patient safety education delivered using the Pecha Kucha teaching method. Group 2 (Scenario-Based Learning Group): Participants will receive patient safety education delivered using a scenario-based teaching method. Group 3 (Control Group): Participants will receive patient safety education delivered using the traditional lecture-based teaching method, which represents the routine educational approach.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

98

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Üsküdar
      • Istanbul, Üsküdar, Tyrkia (Türkiye)
        • University of Health Sciences Turkey

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Being a first-year student at the University of Health Sciences, Hamidiye Faculty of Nursing
  • Attending the "Ethics in Nursing" course
  • Agreeing to participate in the study
  • Being 18 years of age or older
  • Not having previously taken a course on patient safety

Exclusion Criteria:

  • Declining to participate in the study
  • Wishing to withdraw from the study at any stage
  • Incompletely filling out the study's data collection form.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Pecha Kucha Group
Participants will receive patient safety education delivered using the Pecha Kucha teaching method. The intervention consists of a structured presentation format designed to promote active learning, engagement, and concise knowledge delivery.
Participants will receive patient safety education delivered using the Pecha Kucha teaching method. The intervention consists of a structured presentation format designed to promote active learning, engagement, and concise knowledge delivery.
Eksperimentell: Scenario-Based Learning Group
Participants will receive patient safety education delivered using a scenario-based teaching method. The intervention incorporates realistic clinical scenarios to enhance critical thinking, clinical reasoning, and decision-making related to patient safety.
Participants will receive patient safety education delivered using a scenario-based teaching method. The intervention incorporates realistic clinical scenarios to enhance critical thinking, clinical reasoning, and decision-making related to patient safety.
Aktiv komparator: Control Group
Participants will receive patient safety education through the traditional lecture-based teaching method routinely used in the nursing curriculum.
Participants will receive patient safety education through the traditional lecture-based teaching method routinely used in the nursing curriculum.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Medical Error Attitude Scale (MEAS)
Tidsramme: Baseline (before the intervention) and immediately after the intervention

Participants' attitudes toward medical errors will be assessed using the Medical Error Attitude Scale (MEAS). Total scale scores will be compared among the Pecha Kucha, scenario-based learning, and control groups to evaluate the effectiveness of the educational interventions.

The instrument consists of 16 items across three subscales: Perception of Medical Errors, Approach to Medical Errors, and Causes of Medical Errors. Each item is rated on a 5-point Likert scale, and the overall score ranges from 1 to 5. A mean score of 3 or higher indicates a positive attitude toward medical errors, whereas a score below 3 indicates a negative attitude. Higher scores indicate more positive attitudes toward medical error prevention, reporting, and patient safety.

Baseline (before the intervention) and immediately after the intervention

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Adult Education Satisfaction Scale (AESS)
Tidsramme: Immediately after the intervention

Participants' satisfaction with the educational intervention will be evaluated using the Adult Education Satisfaction Scale. Total scale scores will be assessed immediately after completion of the educational intervention to determine participants' satisfaction with the teaching methods.

The scale comprises 30 items organized into six subscales and is scored on a 5-point Likert scale, yielding a total score ranging from 30 to 150. Higher scores indicate greater satisfaction with the educational intervention. The AESS evaluates participants' satisfaction with the educational program and the extent to which it achieves its intended learning objectives.

Immediately after the intervention

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Semra Aciksoz, University of Health Sciences Turkey, Hamidiye Faculty of Nursing

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

24. april 2026

Primær fullføring (Faktiske)

1. juni 2026

Studiet fullført (Faktiske)

1. juli 2026

Datoer for studieregistrering

Først innsendt

4. september 2026

Først innsendt som oppfylte QC-kriteriene

12. september 2026

Først lagt ut (Faktiske)

16. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

16. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

12. september 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • UHealthScience SemraAciksoz

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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