<?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>IRCT20211027052890N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-02-27</date_registration>
      <primary_sponsor>Iran University of Medical Sciences</primary_sponsor>
      <public_title>Designing an educational intervention based on the control source and coping styles of Andler and Parker and its effect on the resilience of nurses nurses in hospitals of Iran University of Medical Sciences during corona outbreak</public_title>
      <acronym></acronym>
      <scientific_title>Designing an educational intervention based on the control source and coping styles of Andler and Parker and its effect on the resilience of nurses nurses in hospitals of Iran University of Medical Sciences during corona outbreak</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-01-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>166</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/59727</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Other design features: This study does not have unique design specifications, Randomization description: Among the hospitals of affiliated to Iran University of Medical Sciences in Tehran city, two hospitals were selected using a dice. To promote the intervention fidelity and reduce the between-group contamination. one of the hospitals will be selected randomly as the control group and the other as the intervention group. Then, 83 nurses, who have the inclusion criteria of the study, will be enrolled from each hospital by systematic random sampling methodach hospital.</study_design>
      <phase>N/A</phase>
      <hc_freetext>The effect of educational intervention on improving nurses' resilience during coronary heart disease.</hc_freetext>
      <i_freetext>Intervention 1: First, the questionnaires were completed in two groups and then an appropriate intervention with the observed weaknesses, in the form of integrated training of various coping strategies with Andler and Parker and control source theory for the experimental group in several sessions through lectures, group discussions, questions and Answers and exercises are provided. Then, the data are entered immediately, 6, 3, 1 month after the intervention in SPSS software version 24 and are analyzed based on the results of pre-test data analysis, and the effectiveness of training in the experimental group is evaluated and also compared with the control group. To take. They are also given CDs and training manuals. Intervention 2: Control group: At the end of the 3-month course of completing the questionnaire by the two groups, a two-hour training session on coping styles will be conducted 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>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 results only will be published in the article</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>mahasti Emami Hamzehkolaee</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Iran university of Medical Sciences, Shahid Hemmat highway, Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1449614535</zip>
        <telephone>+98 21 8670 4756</telephone>
        <email>mahastiemami1@gmail.com</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mahasti Emami Hamzehkolaee</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Mr. Nasser Emami's personal home , Tohid 2,  Western Belt, Babol Town</address>
        <city>Babol</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4714755563</zip>
        <telephone>+98 11 3233 9176</telephone>
        <email>mahastiemami1@gmail.com</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Have at least 5 years of work experience
A history of active care for at least 6 months in the reception wards of patients with coronary heart disease
Having a bachelor's degree or higher</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having a history of physical and mental illness and taking medications that affect the mental system
Absence of more than one session
Loss of a first-degree relative (father, mother, spouse or child) less than six months ago</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>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>First, the questionnaires were completed in two groups and then an appropriate intervention with the observed weaknesses, in the form of integrated training of various coping strategies with Andler and Parker and control source theory for the experimental group in several sessions through lectures, group discussions, questions and Answers and exercises are provided. Then, the data are entered immediately, 6, 3, 1 month after the intervention in SPSS software version 24 and are analyzed based on the results of pre-test data analysis, and the effectiveness of training in the experimental group is evaluated and also compared with the control group. To take. They are also given CDs and training manuals.</i_keyword>
      <i_keyword>Control group: At the end of the 3-month course of completing the questionnaire by the two groups, a two-hour training session on coping styles will be conducted for the control group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Mean score of Connor and Davidson resilience questionnaire in experimental and control groups. Timepoint: The mean scores of the resilience questionnaire were measured at the beginning of the study and immediately, 1 , 3 , 6 months after the intervention. Method of measurement: How to measure the outcome variable is Connor and Davidson Resilience Questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Mean Score of the CISS Standardized Coping Strategies Questionnaire in both experimental and control groups. Timepoint: The mean scores of the CISS Coping Strategies Questionnaire were measured at the beginning of the study and immediately, one month and 3 months after the intervention. Method of measurement: How to measure the variable of coping strategies, 48 question questionnaire of coping strategies is ciss.</sec_outcome>
      <sec_outcome>Mean score of the researcher-made questionnaire of the control source in the field of resilience in both experimental and control groups. Timepoint: The mean scores of the researcher-made questionnaire on resilience were measured at the beginning of the study and immediately, one month and 3 months after the intervention. Method of measurement: How to measure the control source variable in the field of resilience is a researcher-made questionnaire that is used after psychometrics.</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>Iran University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-08-24</approval_date>
        <contact_name>Ethics Committee of Iran University of Medical Sciences and Health Services</contact_name>
        <contact_address>Mr. Nasser Emami's personal home, Tohid 2,  Western Belt, Babol Town Babol Mazandaran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
