<?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>IRCT20231226060534N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-01-28</date_registration>
      <primary_sponsor>Sabzevar University of Medical Sciences</primary_sponsor>
      <public_title>Comparison of the effect of E-learning (webinar) and gamification training based on the model of nursing "Promoting psychological security and empowerment" on the knowledge and attitude of nurses in the process of caring candidates for organ donation</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of the effect of E-learning (webinar) and gamification training based on the model of nursing "Promoting psychological security and empowerment" on the knowledge and attitude of nurses in the process of caring candidates for organ donation</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-01-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/74676</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Because nurses are supposed to be divided into three different groups, the webinar training group, the gamification training group, and the control group (without training), and the number of nurses employed in all three hospitals that also have the criteria for entering this study is not high, therefore, it is not possible to randomly divide nurses into three groups in every hospital. Interventions may influence each other. Therefore, by using simple randomization and drawing lots, each hospital will be assigned to check one of these three methods randomly, Blinding description: Because the participants (nurses) in this research work in three hospitals; Therefore, each hospital will be assigned to a group randomly that the method of blinding is single-blind, and the participants do not know about their research group.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Candidates for organ donation.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: For the first intervention group (E-learning; webinar):  didactic files and two training sessions in the form of a pre-recorded video for two hours based on the dimensions of the model "Improving mental security and empowering nurses" will be presented through the personnel system on the website of SUMS. Intervention 2: Intervention group: For the second intervention group (gamification training): First, didactic files based on the dimensions of the model "Improving mental security and empowering nurses" are presented and then the email address will be provided as a link to this group, which includes 6 scenarios and each scenario has 4 questions, at the end, if the participant has answered less than 70% of the questions correctly, warning of participate again will be appear and the participant must  reach the limit of determined score. Intervention 3: Control group: No intervention will be done for the control group.</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:
Educational files will be shared at the end. All data can be shared after de-identification.

When:
From 12/1/1402

To whom:
All participants of triple groups

Conditions:
After finishing the study

Where to obtain:
Meysam Porhossein
09158881494
meysamporhossein8@gmail.com

How to obtain:
By calling 09158881494 and sending documents to them

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Meysam Porhossein</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Building A, University of Medical Sciences compound, Shohadaye hastei boulevard, Sabsevar Town</address>
        <city>Sabzevar</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9669153889</zip>
        <telephone>+98 58 3721 3338</telephone>
        <email>meysamporhossein8@gmail.com</email>
        <affiliation>Sabzevar University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Meysam Porhossein</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Building A, University of Medical Sciences compound, Shohadaye hastei boulevard, Sabsevar Town</address>
        <city>Sabzevar</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9669153889</zip>
        <telephone>+98 58 3721 3338</telephone>
        <email>meysamporhossein8@gmail.com</email>
        <affiliation>Sabzevar University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Having at least one encounter with a brain dead patient
Lack of previous training in this field
Interested in participating in research</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Nurses who are in plan period and have less than one month left of their plan period
They have the possibility of changing the workplace from the intensive care units, or transferring to another city</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>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: For the first intervention group (E-learning; webinar):  didactic files and two training sessions in the form of a pre-recorded video for two hours based on the dimensions of the model "Improving mental security and empowering nurses" will be presented through the personnel system on the website of SUMS</i_keyword>
      <i_keyword>Intervention group: For the second intervention group (gamification training): First, didactic files based on the dimensions of the model "Improving mental security and empowering nurses" are presented and then the email address will be provided as a link to this group, which includes 6 scenarios and each scenario has 4 questions, at the end, if the participant has answered less than 70% of the questions correctly, warning of participate again will be appear and the participant must  reach the limit of determined score.</i_keyword>
      <i_keyword>Control group: No intervention will be done for the control group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The knowledge score in the researcher maded questionnaire; Comparison of the knowledge and attitude of nurses in the process of caring candidates for organ donation. Timepoint: Before the start of the intervention and 7 and 30 days after the start of the intervention. Method of measurement: The researcher maded questionnaire; Comparison of the knowledge and attitude of nurses in the process of caring candidates for organ donation.</prim_outcome>
      <prim_outcome>The attitude score in the researcher maded questionnaire; Comparison of the knowledge and attitude of nurses in the process of caring candidates for organ donation. Timepoint: Before the start of the intervention and 7 and 30 days after the start of the intervention. Method of measurement: The researcher maded questionnaire; Comparison of the knowledge and attitude of nurses in the process of caring candidates for organ donation.</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>Sabzevar University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-12-17</approval_date>
        <contact_name>Ethics committee of Sabzevar University of Medical Sciences</contact_name>
        <contact_address>Building A, University of Medical Sciences compound, Shohadaye hastei boulevard, Sabsevar Town Sabzevar Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
