<?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>IRCT20240310061245N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-04-03</date_registration>
      <primary_sponsor>Bagheiat-allah University of Medical Sciences</primary_sponsor>
      <public_title>Audit of Critically ill Patients Transportation’s Process in Emergency Department</public_title>
      <acronym></acronym>
      <scientific_title>Audit of Critically ill Patients Transportation’s Process in Emergency Department</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-05-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>33</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/75954</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Health service research.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Critically ill Patients Transportation’s Process.</hc_freetext>
      <i_freetext>Intervention group: This study is a semi-experimental intervention type in which the standards of the transportation process of critically ill patients will be reviewed based on the audit stages. The audit stages include choosing the subject, determining the characteristics and conditions of the audit, collecting information, comparing the information with the standards, taking action to improve and re-examining the situation. After completing steps one to five, an analysis and summary session will be held by research members and judges based on the information obtained. Interventions will be designed based on this meeting and the appropriate intervention will be done according to the changing situation during the study. In general, the process of this study is as follows:1. Obtaining a letter of introduction from the university to Baqiyatullah (AS) hospital2. Making the necessary arrangements with hospital managers, nursing management and emergency department3. Explaining the method to all nurses in different shifts by the researcher and obtaining the consent of the nurses and the patients and obtaining consent to participate in the study.4. Determining the status of standards for the in-hospital transportation process of critically ill emergency patients to intensive care units based on the patient transportation checklist5. Comparison of the status of the transfer process of existing critically ill patients with the standard patient transfer checklist6. Designing corrective measures according to the information obtained from the previous steps regarding the non-compliance of the current situation of the transportation  process of critically ill patients with the standards of the transportation process of critically ill patients and based on the consensus meeting of the research team and respected referees and finally its implementation by the project manager7. Determining the status of the transfer process of critically ill patients after corrective measures8. Comparison of the status of the transportation process of critically ill patients before and after corrective measures9. Data entry and statistical analysis using SPSS-v 26 statistical software and reporting the results.</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>Yes - There is a plan to make this available</results_IPD_plan>
      <results_IPD_description>What will be shared:
The results of the research and information related to the main outcome are shared.

When:
Beginning of the access period from the end of 1403

To whom:
Researchers of medical centers, hospitals and universities of medical sciences

Conditions:
Data access levels will be granted under the agreement of Hafa and Baqiyatullah University of Medical Sciences.

Where to obtain:
Access and correspondence is possible through the following email:
alireza.abasi1806@gmail.com

How to obtain:
1. Send request by email
2. Submitting the application to the Research Center and Baqiyatullah University of Medical Sciences
3. The final answer to the request

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Alireza Abasi Niyasar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 6, Mikhak 10th Alley, Golestan Blvd, Phase 2, Kashan</address>
        <city>kashan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8719335818</zip>
        <telephone>+98 31 5542 5655</telephone>
        <email>alireza.abasi1806@gmail.com</email>
        <affiliation>Bagheiat-allah University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Hossein  Mahmoodi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Trauma Research Center, Nursing Faculty, Baqiyatallah University of Medical Sciences, Tehran, IR Iran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1435916471</zip>
        <telephone>+98 21 2228 9941</telephone>
        <email>h.mahmoudi@bmsu.ac.ir</email>
        <affiliation>Bagheiat-allah University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Critically ill patients in the emergency department who have been admitted for at least 3 hours and are ready to be transferred to intensive care unit with the doctor's order.
Nurses working permanently in the emergency department
Nurses should have at least two months of experience working in the emergency room
Nurses must have a nursing associate degree, internship or higher.
There is no age limit for patients
Nurses should be between 22 and 60 years old.</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Presence of patients in the emergency department for less than 3 hours
Absence of indication to transport the patient to the intensive care unit</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>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: This study is a semi-experimental intervention type in which the standards of the transportation process of critically ill patients will be reviewed based on the audit stages. The audit stages include choosing the subject, determining the characteristics and conditions of the audit, collecting information, comparing the information with the standards, taking action to improve and re-examining the situation. After completing steps one to five, an analysis and summary session will be held by research members and judges based on the information obtained. Interventions will be designed based on this meeting and the appropriate intervention will be done according to the changing situation during the study. In general, the process of this study is as follows:1. Obtaining a letter of introduction from the university to Baqiyatullah (AS) hospital2. Making the necessary arrangements with hospital managers, nursing management and emergency department3. Explaining the method to all nurses in different shifts by the researcher and obtaining the consent of the nurses and the patients and obtaining consent to participate in the study.4. Determining the status of standards for the in-hospital transportation process of critically ill emergency patients to intensive care units based on the patient transportation checklist5. Comparison of the status of the transfer process of existing critically ill patients with the standard patient transfer checklist6. Designing corrective measures according to the information obtained from the previous steps regarding the non-compliance of the current situation of the transportation  process of critically ill patients with the standards of the transportation process of critically ill patients and based on the consensus meeting of the research team and respected referees and finally its implementation by the project manager7. Determining the status of the transfer process of critically ill patients after corrective measures8. Comparison of the status of the transportation process of critically ill patients before and after corrective measures9. Data entry and statistical analysis using SPSS-v 26 statistical software and reporting the results</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Patient transportation process standards. Timepoint: Examining the standards of the patient transportation process at the beginning of the study (before the start of the intervention) and 3 days after the intervention. Method of measurement: Checklist of patient transportation process standards.</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>Bagheiat-allah University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-03-04</approval_date>
        <contact_name>Research Ethics Committees of Baqiyatallah Hospital</contact_name>
        <contact_address>Baqiyatallah university of medical science, Vanak square, Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
