<?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>IRCT20181015041350N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-10-30</date_registration>
      <primary_sponsor>Artesh University of Medical Sciences</primary_sponsor>
      <public_title>The Effect of Education on knowledge, Attitude and Practice of Nurses</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the Effect of Lecture Training and Clinical Education on the Care of Patients with Angina Pectoris on Knowledge, Attitude and Practice of Nurses in Emergency Department of Military Hospitals of Mashhad.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-11-11</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/34589</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In this study, firstly, nurses of the emergency department after the explanation of the research goals will be based on simple random sampling criteria in two groups of test and one control group. The knowledge, attitude and practice of nurses before and after the implementation of the curriculum (lecture-clinical education) will be investigated.Before the intervention, the pre-test will be held in three groups.Immediately and one month after the intervention, all participants will receive a post-test.The practice questionnaire will be completed by the researcher.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Nurses in Emergency Department of Military Hospitals of Mashhad..</hc_freetext>
      <i_freetext>Intervention 1: Intervention group First: Group Lecture Training Education: The number of nurses in the classroom will be better for learning, with a minimum of 5 people and a maximum of 15 people. Accidentally, each hospital will be in one of three groups (lecture group, clinical education, control). The number of samples in the three hospitals will be the same. The training place is at conference halls of military hospitals in Mashhad. Training for nurses will be done in a 5-hour session. The knowledge and attitude questionnaire will be completed immediately and one month after the completion of the training sessions by the units under study. A practice questionnaire is completed by the researcher at the same time that will examine the proper functioning of nurses in training for patients with angina pectoris. Intervention 2: Intervention group Second: Group Clinical Education: The place of education in the bedside of patients with angina pectoris will be held in the cardiovascular departments of military hospitals in Mashhad. The number of trainees is maximum 5 people. Training for nurses will be done in a 5-hour session. The knowledge and attitude questionnaire will be completed immediately and one month after the completion of the training sessions by the units under study. A practice questionnaire is completed by the researcher at the same time that will examine the proper functioning of nurses in training for patients with angina pectoris. Intervention 3: Control group: In the intervention group, the investigator will not be accepted and only one pretest and two post-tests will be completed within a month's time interval. In order to observe ethical principles in the research, the contents and training will be given to the control group upon completion of the research.</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:
Sharing after the study.

When:
Sharing after the study.

To whom:
After the end of the study, be distributed to researchers working in academic and academic institutions.

Conditions:
After the end of the study, summarize the article for scholars working in academic and scientific institutions.

Where to obtain:
After the end of the study, email address applicants will be shared.

How to obtain:
After the end of the study, applicants can request access to files by visiting an email address.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Reza Yousefi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 29, Ahangaran Street, Square 7 Tir.</address>
        <city>Sabzevar</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9616689854</zip>
        <telephone>+98 51 4445 1787</telephone>
        <email>reza.yousefi2015@yahoo.com</email>
        <affiliation>Artesh University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Reza Yousefi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>N0 29,  7 Tir Square, Ahangaran Ave.</address>
        <city>Sabzevar</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9616689854</zip>
        <telephone>+98 51 4445 1787</telephone>
        <email>reza.yousefi2015@yahoo.com</email>
        <affiliation>Artesh 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 a minimum degree of nursing expert
Not having a history of teaching (theoretical and practical) regarding angina pectoris in the last six months
Wish to participate in the study
Having at least one year of Clinical work in Emergency or in a CCU Section</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Unwillingness to continue cooperation in research
People who miss more than 30% of the course
Failure to complete pre-test or post-test</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>Behavior</i_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group First: Group Lecture Training Education: The number of nurses in the classroom will be better for learning, with a minimum of 5 people and a maximum of 15 people. Accidentally, each hospital will be in one of three groups (lecture group, clinical education, control). The number of samples in the three hospitals will be the same. The training place is at conference halls of military hospitals in Mashhad. Training for nurses will be done in a 5-hour session. The knowledge and attitude questionnaire will be completed immediately and one month after the completion of the training sessions by the units under study. A practice questionnaire is completed by the researcher at the same time that will examine the proper functioning of nurses in training for patients with angina pectoris.</i_keyword>
      <i_keyword>Intervention group Second: Group Clinical Education: The place of education in the bedside of patients with angina pectoris will be held in the cardiovascular departments of military hospitals in Mashhad. The number of trainees is maximum 5 people. Training for nurses will be done in a 5-hour session. The knowledge and attitude questionnaire will be completed immediately and one month after the completion of the training sessions by the units under study. A practice questionnaire is completed by the researcher at the same time that will examine the proper functioning of nurses in training for patients with angina pectoris.</i_keyword>
      <i_keyword>Control group: In the intervention group, the investigator will not be accepted and only one pretest and two post-tests will be completed within a month's time interval. In order to observe ethical principles in the research, the contents and training will be given to the control group upon completion of the research</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Knowledge Score from knowledge Questionnaire. Timepoint: Knowledge score at the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Knowledge Questionnaire which is made by the researcher.</prim_outcome>
      <prim_outcome>Attitude Score of Attitude Questionnaire. Timepoint: Attitude score at the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Attitude Questionnaire which is made by the researcher.</prim_outcome>
      <prim_outcome>Practice Score of the Practice Questionnaire. Timepoint: Practice score at the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Practice Questionnaire which is made by the researcher.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Knowledge of Nurses on how to care for patients with angina pectoris. Timepoint: Knowledge of Nursesat the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Short Knowledge Questionnaire 18 questions which is made by the researcher.</sec_outcome>
      <sec_outcome>Attitude of Nurses on how to care for patients with angina pectoris. Timepoint: Attitude  of Nursesat the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Short Attitude Questionnaire 7 questions which is made by the researcher.</sec_outcome>
      <sec_outcome>Practice of Nurses on how to care for patients with angina pectoris. Timepoint: Practice of Nursesat the beginning of the study (before the intervention) and immediately and one month after the intervention. Method of measurement: Short Practice Questionnaire 24 questions which is made by the researcher.</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>Artesh University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-10-14</approval_date>
        <contact_name>Ethics Committee of Aja University of Medical Science</contact_name>
        <contact_address>West Fatemi St. - Shahid Etemadzadeh Avenue - Aja University of Medical Science Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
