<?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>IRCT20231022059812N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2023-12-12</date_registration>
      <primary_sponsor>Esfahan University of Medical Sciences</primary_sponsor>
      <public_title>Investigating the effect of a program based on cognitive behavioral therapy of horizontal violence</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the effect of the program based on cognitive behavioral therapy on the horizontal violence of nurses in the emergency department of the hospital.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2023-11-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>122</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/73763</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Not randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Education/Guidance.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Investigating the effect of a program based on cognitive behavioral therapy on horizontal violence of emergency department nurses.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: In this study, in order to carry out the research, the researcher, after the approval of the ethics committee of Isfahan University of Medical Sciences and receiving a sampling permit from the Research Vice-Chancellor of the Faculty of Nursing and Midwifery of the University of Medical Sciences, went to He went to Al-Zahra Medical Training Center (S) in Isfahan and after explaining the objectives of the research to the relevant officials, he will attend the emergency department to access the studied samples. The current research is a two-group, two-stage clinical trial with a before-and-after design. In this research, after the researcher explained the objectives of the study and the confidentiality of the information, informed consent will be obtained from the participants to participate in the research. Then they will be randomly assigned to intervention and control groups based on the entry criteria. Before starting the interventions, all the participants answered the questionnaire of Demont (2012) and in order to respect the confidentiality of the information, the door of the response envelopes will be closed.The interventions of this research is a program based on cognitive behavioral therapy, which in the form of a combined package includes: holding cognitive-behavioral therapy training sessions with a focus on anger management and improving communication skills for managers and nurses along with compiling a booklet with the content of horizontal violence in order to promote The ways of interaction and communication will be in the emergency department. The training sessions will be in the form of ten ninety-minute sessions with an interval of one week. The sessions will be taught by a student and a clinical psychology specialist, and in order to fully prepare for teaching the content, the student has participated in a cognitive behavioral therapy training course and received a certificate. will take the relevant.The meeting place will be one of the educational classes of Al-Zahra Hospital (S), which will be coordinated with the relevant official to reserve the class. After completing the interventions for the intervention group and completing the questionnaires, a booklet on the concept of violence will be provided to the control group, and a training session will be provided to the control group to familiarize them with the concept of violence. Data analysis and intervention effectiveness evaluation will be done with covariance analysis and SPSS software. Intervention 2: Control group: In this study, in order to carry out the research, the researcher, after the approval of the ethics committee of Isfahan University of Medical Sciences and receiving a sampling permit from the Research Vice-Chancellor of the Faculty of Nursing and Midwifery of the University of Medical Sciences,He went to Al-Zahra Medical Training Center (S) in Isfahan and after explaining the objectives of the research to the relevant officials, he will attend the emergency department to access the studied samples. The current research is a two-group, two-stage clinical trial with a before-and-after design. In this research, after the researcher explained the objectives of the study and the confidentiality of the information, informed consent will be obtained from the participants to participate in the research. Then they will be randomly assigned to intervention and control groups based on the entry criteria. Before starting the interventions, all the participants answered the questionnaire of Demont (2012) and in order to respect the confidentiality of the information, the door of the response envelopes will be closed.After completing the interventions for the intervention group and completing the questionnaires, a booklet on the concept of violence will be provided to the control group, and a training session will be provided to the control group to familiarize them with the concept of violence.</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 There is no further information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Shima Safazadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Isfahan, Iran</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8174673461</zip>
        <telephone>+98 31 1792 2904</telephone>
        <email>safa_sh58@yahoo.com</email>
        <affiliation>Esfahan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Shima Safazadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Isfahan, Iran</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8174673461</zip>
        <telephone>+98 31 1792 2904</telephone>
        <email>safa_sh58@yahoo.com</email>
        <affiliation>Esfahan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Nurses working in the emergency department with a bachelor's degree in nursing or higher
Having at least one year of clinical work experience in the emergency department
Absence of mental disorders according to DSM 5
Full consent to participate in the research</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Do not want to continue participating in the study
transfer to another department or leaving the center during the study
Incomplete completion of the research questionnaire
Absence of more than 3 sessions in training programs</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>N/A</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: In this study, in order to carry out the research, the researcher, after the approval of the ethics committee of Isfahan University of Medical Sciences and receiving a sampling permit from the Research Vice-Chancellor of the Faculty of Nursing and Midwifery of the University of Medical Sciences, went to He went to Al-Zahra Medical Training Center (S) in Isfahan and after explaining the objectives of the research to the relevant officials, he will attend the emergency department to access the studied samples. The current research is a two-group, two-stage clinical trial with a before-and-after design. In this research, after the researcher explained the objectives of the study and the confidentiality of the information, informed consent will be obtained from the participants to participate in the research. Then they will be randomly assigned to intervention and control groups based on the entry criteria. Before starting the interventions, all the participants answered the questionnaire of Demont (2012) and in order to respect the confidentiality of the information, the door of the response envelopes will be closed.The interventions of this research is a program based on cognitive behavioral therapy, which in the form of a combined package includes: holding cognitive-behavioral therapy training sessions with a focus on anger management and improving communication skills for managers and nurses along with compiling a booklet with the content of horizontal violence in order to promote The ways of interaction and communication will be in the emergency department. The training sessions will be in the form of ten ninety-minute sessions with an interval of one week. The sessions will be taught by a student and a clinical psychology specialist, and in order to fully prepare for teaching the content, the student has participated in a cognitive behavioral therapy training course and received a certificate. will take the relevant.The meeting place will be one of the educational classes of Al-Zahra Hospital (S), which will be coordinated with the relevant official to reserve the class. After completing the interventions for the intervention group and completing the questionnaires, a booklet on the concept of violence will be provided to the control group, and a training session will be provided to the control group to familiarize them with the concept of violence. Data analysis and intervention effectiveness evaluation will be done with covariance analysis and SPSS software</i_keyword>
      <i_keyword>Control group: In this study, in order to carry out the research, the researcher, after the approval of the ethics committee of Isfahan University of Medical Sciences and receiving a sampling permit from the Research Vice-Chancellor of the Faculty of Nursing and Midwifery of the University of Medical Sciences,He went to Al-Zahra Medical Training Center (S) in Isfahan and after explaining the objectives of the research to the relevant officials, he will attend the emergency department to access the studied samples. The current research is a two-group, two-stage clinical trial with a before-and-after design. In this research, after the researcher explained the objectives of the study and the confidentiality of the information, informed consent will be obtained from the participants to participate in the research. Then they will be randomly assigned to intervention and control groups based on the entry criteria. Before starting the interventions, all the participants answered the questionnaire of Demont (2012) and in order to respect the confidentiality of the information, the door of the response envelopes will be closed.After completing the interventions for the intervention group and completing the questionnaires, a booklet on the concept of violence will be provided to the control group, and a training session will be provided to the control group to familiarize them with the concept of violence.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Horizontal violence score based on Dumont 2012 horizontal violence questionnaire. Timepoint: before and after the intervention and one month after completing the study. Method of measurement: Dumont Horizontal Violence Questionnaire 2012.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Horizontal violence score based on Dumont 2012 horizontal violence questionnaire. Timepoint: before and after the intervention and one month after the completion of the study. Method of measurement: Dumont Horizontal Violence Questionnaire 2012.</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>Esfahan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-10-18</approval_date>
        <contact_name>Ethics Committee of Isfahan University of Medical Sciences</contact_name>
        <contact_address>Faculty of Nursing and Midwifery, Isfahan University of Medical Sciences, Hazar Jarib Street ISFAHAN Isfehan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
