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CPR and Agonal Breathing Recognition Training for Police Officers (CPR-AB Police)

6. juli 2026 oppdatert av: Hua Ho, Far Eastern Memorial Hospital

Evaluation of CPR Training and Agonal Breathing Recognition Among New Taipei City Police Officers in Out-of-Hospital Cardiac Arrest Events

This study will evaluate an educational training program for police officers in New Taipei City, Taiwan. Police officers may arrive at out-of-hospital cardiac arrest events before emergency medical services and may be able to provide early cardiopulmonary resuscitation and automated external defibrillator support. However, abnormal gasping or agonal breathing can be mistaken for normal breathing and may delay recognition of cardiac arrest.

Participants will receive a single training session consisting of an adult CPR refresher course and agonal breathing recognition training. Anonymous online questionnaires will be completed before and immediately after the training. The study will compare pre-training and post-training questionnaire results to assess changes in agonal breathing recognition accuracy, CPR-related knowledge, and course satisfaction.

Studieoversikt

Detaljert beskrivelse

This is a single-arm, before-and-after educational intervention study conducted among active police officers in New Taipei City, Taiwan. The study is embedded in routine annual first aid training for police officers.

The intervention consists of a single training session. The first component is a 20-minute adult CPR refresher course covering the emergency response sequence, chest compression quality, compression depth and rate, and complications of chest compression. The second component is a 40-minute agonal breathing recognition session covering the pathophysiology and clinical presentation of agonal breathing, video-based recognition practice using real cases, and analysis of common recognition errors.

Before the training session, study information is provided and participants are invited to complete an anonymous online pre-training questionnaire using a QR code. Immediately after the training session, participants are invited to complete an anonymous online post-training questionnaire using a QR code. Questionnaire data will be used to evaluate changes in agonal breathing recognition accuracy, CPR-related knowledge, and overall learning outcomes. Course satisfaction will be assessed using the post-training questionnaire.

Participation is voluntary. The study collects anonymous questionnaire responses and does not involve patient-level clinical data or direct patient intervention. There is no long-term participant follow-up.

Studietype

Intervensjonell

Registrering (Faktiske)

3439

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

      • New Taipei City, Taiwan, 220
        • Far Eastern Memorinal Hospital

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:

  • Active police officers serving in New Taipei City, Taiwan
  • Officers attending routine annual first aid or CPR training
  • Officers who voluntarily complete the anonymous online pre-training and/or post-training questionnaire

Exclusion Criteria:

- None

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Helsetjenesteforskning
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: CPR Refresher and Agonal Breathing Recognition Training
Participants receive a single-session educational intervention consisting of adult CPR refresher training and agonal breathing recognition training. Anonymous online questionnaires are completed immediately before and immediately after the training session.
A single-session educational training program consisting of a 20-minute adult CPR refresher course and a 40-minute agonal breathing recognition training session. The CPR refresher covers the emergency response sequence, chest compression quality, compression depth and rate, and complications of chest compression. The agonal breathing recognition session covers pathophysiology, clinical presentation, real-case video-based recognition practice, and analysis of common recognition errors.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Agonal Breathing Recognition Accuracy
Tidsramme: Immediately before and immediately after the training session
Difference between pre-training and post-training accuracy in recognizing agonal breathing, measured using a study-specific anonymous online questionnaire.
Immediately before and immediately after the training session

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in CPR-Related Knowledge Score
Tidsramme: Immediately before and immediately after the training session
Difference between pre-training and post-training CPR-related knowledge scores, measured using a study-specific anonymous online questionnaire.
Immediately before and immediately after the training session
Change in Total Learning Outcome Score
Tidsramme: Immediately before and immediately after the training session
Difference between pre-training and post-training total questionnaire scores, measured using a study-specific anonymous online questionnaire.
Immediately before and immediately after the training session
Course Satisfaction Score
Tidsramme: Immediately after the training session
Course satisfaction measured using a study-specific anonymous online post-training questionnaire.
Immediately after the training session

Samarbeidspartnere og etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

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)

12. juni 2026

Primær fullføring (Faktiske)

30. juni 2026

Studiet fullført (Faktiske)

30. juni 2026

Datoer for studieregistrering

Først innsendt

6. juli 2026

Først innsendt som oppfylte QC-kriteriene

6. juli 2026

Først lagt ut (Faktiske)

10. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. juli 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 115159-W (Annen identifikator: IRB / Research Ethics Review Committee exemption approval number, Far Eastern Memorial Hospital)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Individual participant data will not be shared publicly because this study collects anonymous questionnaire responses in an occupational training setting, and public sharing of participant-level data was not included in the ethics-approved protocol. Study-related electronic data will be accessible only to the research team, stored securely, and deleted after the approved retention period. Aggregated results may be reported in conference presentations and journal publications.

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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