<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE trials [
<!ELEMENT trials (trial+)>

<!ELEMENT trial (main,contacts,countries,criteria,health_condition_code,health_condition_keyword,intervention_code,
          intervention_keyword,primary_outcome,secondary_outcome,secondary_sponsor,secondary_ids,source_support,ethics_reviews)>

<!ELEMENT main (trial_id,utrn?,reg_name,date_registration,primary_sponsor,public_title,acronym?,scientific_title,scientific_acronym?,
          date_enrolment,type_enrolment,target_size,recruitment_status,url?,study_type,study_design,phase,hc_freetext?,i_freetext?,results_actual_enrolment,results_date_completed,results_url_link,results_summary,           results_date_posted,results_date_first_publication,results_baseline_char,results_participant_flow,results_adverse_events,results_outcome_measures,results_url_protocol,results_IPD_plan, results_IPD_description)>
<!ELEMENT trial_id (#PCDATA)>
<!ELEMENT utrn (#PCDATA)>
<!ELEMENT reg_name (#PCDATA)>
<!ELEMENT date_registration (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT primary_sponsor (#PCDATA)>
<!ELEMENT public_title (#PCDATA)>
<!ELEMENT acronym (#PCDATA)>
<!ELEMENT scientific_title (#PCDATA)>
<!ELEMENT scientific_acronym (#PCDATA)>
<!ELEMENT date_enrolment (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT type_enrolment (#PCDATA)>
<!ELEMENT target_size (#PCDATA)>
<!ELEMENT recruitment_status (#PCDATA)><!-- Pending,Recruiting,Suspended,Complete,Other -->
<!ELEMENT url (#PCDATA)>
<!ELEMENT study_type (#PCDATA)><!-- interventional,observational -->
<!ELEMENT study_design (#PCDATA)>
<!ELEMENT phase (#PCDATA)>
<!ELEMENT hc_freetext (#PCDATA)>
<!ELEMENT i_freetext (#PCDATA)>
<!ELEMENT results_actual_enrolment (#PCDATA)>
<!ELEMENT results_date_completed (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_url_link (#PCDATA)>
<!ELEMENT results_summary (#PCDATA)>
<!ELEMENT results_date_posted (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_date_first_publication (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_baseline_char (#PCDATA)>
<!ELEMENT results_participant_flow (#PCDATA)>
<!ELEMENT results_adverse_events (#PCDATA)>
<!ELEMENT results_outcome_measures (#PCDATA)>
<!ELEMENT results_url_protocol (#PCDATA)>
<!ELEMENT results_IPD_plan (#PCDATA)>
<!ELEMENT results_IPD_description (#PCDATA)>


<!ELEMENT contacts (contact+)>
<!ELEMENT contact (type,firstname,middlename,lastname,address,city,country1,zip,telephone,email,affiliation)>
<!ELEMENT type (#PCDATA)><!-- Public,Scientific -->
<!ELEMENT firstname (#PCDATA)>
<!ELEMENT middlename (#PCDATA)>
<!ELEMENT lastname (#PCDATA)>
<!ELEMENT address (#PCDATA)>
<!ELEMENT city (#PCDATA)>
<!ELEMENT country1 (#PCDATA)>
<!ELEMENT zip (#PCDATA)>
<!ELEMENT telephone (#PCDATA)>
<!ELEMENT email (#PCDATA)>
<!ELEMENT affiliation (#PCDATA)>

<!ELEMENT countries (country2+)>
<!ELEMENT country2 (#PCDATA)>

<!ELEMENT criteria (inclusion_criteria,agemin,agemax,gender,exclusion_criteria)>
<!ELEMENT inclusion_criteria (#PCDATA)>
<!ELEMENT agemin (#PCDATA)>
<!ELEMENT agemax (#PCDATA)>
<!ELEMENT gender (#PCDATA)>
<!ELEMENT exclusion_criteria (#PCDATA)>

<!ELEMENT health_condition_code (hc_code+)>
<!ELEMENT hc_code (#PCDATA)>

<!ELEMENT health_condition_keyword (hc_keyword+)>
<!ELEMENT hc_keyword (#PCDATA)>

<!ELEMENT intervention_code (i_code+)>
<!ELEMENT i_code (#PCDATA)>

<!ELEMENT intervention_keyword (i_keyword+)>
<!ELEMENT i_keyword (#PCDATA)>

<!ELEMENT primary_outcome (prim_outcome+)>
<!ELEMENT prim_outcome (#PCDATA)>

<!ELEMENT secondary_outcome (sec_outcome+)>
<!ELEMENT sec_outcome (#PCDATA)>

<!ELEMENT secondary_sponsor (sponsor_name+)>
<!ELEMENT sponsor_name (#PCDATA)>

<!ELEMENT secondary_ids (secondary_id+)>
<!ELEMENT secondary_id (sec_id,issuing_authority)>
<!ELEMENT sec_id (#PCDATA)>
<!ELEMENT issuing_authority (#PCDATA)>

<!ELEMENT source_support (source_name+)>
<!ELEMENT source_name (#PCDATA)>

<!ELEMENT ethics_reviews (ethics_review+)>
<!ELEMENT ethics_review (status,approval_date,contact_name,contact_address,contact_phone,contact_email)>
<!ELEMENT status (#PCDATA)><!-- Not approved,Approved,NA -->
<!ELEMENT approval_date (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT contact_name (#PCDATA)>
<!ELEMENT contact_address (#PCDATA)>
<!ELEMENT contact_phone (#PCDATA)>
<!ELEMENT contact_email (#PCDATA)>
]>
<trials>
  <trial>
    <main>
      <trial_id>IRCT20260713070159N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-07-26</date_registration>
      <primary_sponsor>Qazvin University of Medical Sciences</primary_sponsor>
      <public_title>Training Nursing Students in ESI Triage Using the BOPPS-CBL Method</public_title>
      <acronym></acronym>
      <scientific_title>The Effect of ESI Triage Training Using the BOPPS-CBL Method on Nursing Students’ Knowledge and decision-making Based on Kirkpatrick’s Evaluation Model</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-08-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>33</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/91601</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: After meeting the eligibility criteria, participants will be randomly assigned to either the intervention group (BOPPS–CBL) or the control group (LBL). Randomization will be performed by a statistician using R software. A block randomization or simple randomization method will be employed where generated random numbers will determine group assignment: even numbers will be allocated to the intervention group, and odd numbers to the control group. To ensure allocation concealment, the randomization sequence will be generated by an individual not involved in the research team.

Blinding:

Due to the educational nature of the intervention, blinding of participants and instructors is not feasible. However, to minimize assessment bias, the outcome assessors will be blinded to the group assignment (single-blind design).</study_design>
      <phase>N/A</phase>
      <hc_freetext>.</hc_freetext>
      <i_freetext>Intervention 1: The intervention group will receive triage training based on the Emergency Severity Index using a combined six-stage instructional framework consisting of bridge-in, objectives, pre-assessment, participatory learning, post-assessment, and summary, integrated with scenario-based learning. The intervention will consist of two 60-minute educational sessions delivered on the same day by master’s students in emergency nursing. The educational content will include the foundations of triage, the definition and history of triage, the need for and objectives of a triage unit, the role of triage personnel, resource-based triage, introduction to the five-level Emergency Severity Index system, and differences between the Emergency Severity Index and other triage systems. It will also cover the complete Emergency Severity Index algorithm, decision criteria, under-triage, over-triage, common errors, and prevention strategies. The training will be delivered before class, including motivation, learning objectives, and a short pre-assessment, and during class, including small-group participatory learning, analysis of clinical scenarios, determination of acuity levels and initial actions, group discussion, post-assessment, and summary. Five scenarios will be used in each session. Intervention 2: Control group: The control group will receive triage training based on the Emergency Severity Index through the conventional lecture method. The educational content in this group will be similar to that of the intervention group and will include the foundations of triage, the definition and history of triage, the need for and objectives of a triage unit, the role of triage personnel, resource-based triage, introduction to the five-level Emergency Severity Index system, the Emergency Severity Index algorithm, decision criteria at points A to D, under-triage, over-triage, common decision-making errors, and prevention strategies. The training will be delivered in two 60-minute sessions. Educational materials will be provided to students before the session, and a short period will be allocated at the end of each session for reviewing key points, discussion, questions, and answers.</i_freetext>
      <results_actual_enrolment></results_actual_enrolment>
      <results_date_completed></results_date_completed>
      <results_url_link></results_url_link>
      <results_summary></results_summary>
      <results_date_posted></results_date_posted>
      <results_date_first_publication></results_date_first_publication>
      <results_baseline_char></results_baseline_char>
      <results_participant_flow></results_participant_flow>
      <results_adverse_events></results_adverse_events>
      <results_outcome_measures></results_outcome_measures>
      <results_url_protocol></results_url_protocol>
      <results_IPD_plan>Undecided - It is not yet known if there will be a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for indecision in sharing IPD is The individual participant data will not be shared to protect the confidentiality and privacy of the participating students. Overall results will be published in a peer-reviewed journal.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mojtaba Senmar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Nursing and Midwifery, Qazvin University of Medical Sciences, Bahonar Blvd., Qazvin, Iran</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3415868487</zip>
        <telephone>+98 28 3333 6001</telephone>
        <email>senmarmojtaba@gmail.com</email>
        <affiliation>Qazvin University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mojtaba Senmar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Nursing and Midwifery, Qazvin University of Medical Sciences, Bahonar Blvd., Qazvin, Iran</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3415868487</zip>
        <telephone>+98 28 3333 6001</telephone>
        <email>senmarmojtaba@gmail.com</email>
        <affiliation>Qazvin University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Undergraduate nursing students in their 7th or 8th semesters
Willingness to participate in the research
No prior experience or participation in similar triage training courses before the study</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Withdrawal of consent or unwillingness to continue the study
Incomplete questionnaires or insufficient data (defined as having more than 5% missing data)</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>The intervention group will receive triage training based on the Emergency Severity Index using a combined six-stage instructional framework consisting of bridge-in, objectives, pre-assessment, participatory learning, post-assessment, and summary, integrated with scenario-based learning. The intervention will consist of two 60-minute educational sessions delivered on the same day by master’s students in emergency nursing. The educational content will include the foundations of triage, the definition and history of triage, the need for and objectives of a triage unit, the role of triage personnel, resource-based triage, introduction to the five-level Emergency Severity Index system, and differences between the Emergency Severity Index and other triage systems. It will also cover the complete Emergency Severity Index algorithm, decision criteria, under-triage, over-triage, common errors, and prevention strategies. The training will be delivered before class, including motivation, learning objectives, and a short pre-assessment, and during class, including small-group participatory learning, analysis of clinical scenarios, determination of acuity levels and initial actions, group discussion, post-assessment, and summary. Five scenarios will be used in each session.</i_keyword>
      <i_keyword>Control group: The control group will receive triage training based on the Emergency Severity Index through the conventional lecture method. The educational content in this group will be similar to that of the intervention group and will include the foundations of triage, the definition and history of triage, the need for and objectives of a triage unit, the role of triage personnel, resource-based triage, introduction to the five-level Emergency Severity Index system, the Emergency Severity Index algorithm, decision criteria at points A to D, under-triage, over-triage, common decision-making errors, and prevention strategies. The training will be delivered in two 60-minute sessions. Educational materials will be provided to students before the session, and a short period will be allocated at the end of each session for reviewing key points, discussion, questions, and answers.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Nursing students’ knowledge score regarding Emergency Severity Index triageNursing students’ decision-making score regarding Emergency Severity Index triage. Timepoint: Before the intervention, one week after the intervention, and one month after the intervention. Method of measurement: Emergency Severity Index Knowledge QuestionnaireTriage Decision-Making Questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome></sec_outcome>
    </secondary_outcome>
    <secondary_sponsor>
      <sponsor_name></sponsor_name>
    </secondary_sponsor>
    <secondary_ids>
      <secondary_id>
        <sec_id></sec_id>
        <issuing_authority></issuing_authority>
      </secondary_id>
    </secondary_ids>
    <source_support>
      <source_name>Qazvin University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-06-07</approval_date>
        <contact_name>Ethics Committee of Qazvin University of Medical Sciences</contact_name>
        <contact_address>Ethics Committee Unit, Research Ethics Committee, Vice Presidency for Research and Technology, Qazvin University of Medical Sciences, 1st Floor, No. 16, Modat Alley, opposite Shahid Beheshti Park, before Valiasr Crossroads, Shahid Beheshti Blvd, Qazvin, Iran. Qazvin Qazvin Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
