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Studying the effect of 115 triage experts' guidance on scene witnesses on the outcome of patients with cardiac arrest

Studying the effect of empowering prehospital emergency telephone triage personnel based on a four-level model in guiding basic resuscitation by witnesses on the outcome of patients with cardiac and respiratory arrest

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241106063618N1
Enrollment
100
Registered
2025-01-17
Start date
2024-12-09
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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Interventions

This study is a pre-post clinical trial that will be conducted on personnel working in the pre-hospital emergency telephone triage unit of Hamadan province. For this purpose, all telephone resuscitati

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Entry criteria: Level One: (Triage personnel) Willingness to participate in the research Level two: (Calls recorded as cardiac arrest) calls recorded to the pre-hospital emergency room with complaints of cardiac and respiratory arrest, in order to control confounding variables such as the average time of arrival of the ambulance in both periods of this time in the range of 8 to 15 minutes will be included in the study, and if there is too much time in both periods, the sample will be excluded from the study, and when evaluating the results, the average time of ambulance arrival in both periods will be reported

Exclusion criteria

Exclusion criteria: Level one (triage personnel): Absence of more than one session in the training course, refusal to participate in the research Level two (calls recorded as cardiac arrest): Incomplete registration of the patient's medical record in the pre-hospital emergency system, if the patient's companion is part of the treatment staff or has undergone cardiopulmonary resuscitation in both periods, the study is excluded. becomes Lack of trainability of the witness at the scene due to age or physical limitations

Design outcomes

Primary

MeasureTime frame
Outcomes of cardiopulmonary resuscitation. Timepoint: 6 months. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJafar hemati

Qazvin University of Medical Sciences

amir.hemati7272@gmail.com+98 81 3485 3585

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026