<?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>IRCT20220118053758N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-06-25</date_registration>
      <primary_sponsor>Esfahan University of Medical Sciences</primary_sponsor>
      <public_title>Investigating the effect of self-study training on resilience and effective coping styles in women involved in domestic violence</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the effect of self-study training on resilience and effective coping styles in women involved in domestic violence referred to Isfahan Comprehensive Health Service Centers in 2022</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-05-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>64</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/62927</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, first, pre-test to identify women at risk of violence against spouses in the form of a standard questionnaire to measure violence against women for women referring to comprehensive health care centers. After the positive result of the test using the lottery method, 64 of them will be divided into two experimental and control groups. In this method, the researcher gives a special number to each member of the community. Then they are mixed in a container. In the next step, she takes out the numbers one by one and takes notes, This operation is continued until the number of samples is selected and then the experimental and control groups are selected using the same method.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Condition 1: . Condition 2: . Condition 3: .</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: The intervention group is divided into two groups of 16 people and each of them will be given a Meichenbaum self-study group training in 7 sessions of 60 minutes in a two-month course. self-study is a technique of the CBT approach that is an exercise to improve self-control and self-talk is used to stimulate and reinforce during treatment. The self-study technique uses positive verbal expressions to reduce negative thoughts and to increase self-control through the mind. The most important step in the self-learning technique is that the person begins to speak slowly in their heart. after completing the training resilience score and coping style score using Connor and Davidson resilience scale (CD-RISC) and Lazarus and Folkman's coping style questionnaire (WOCQ) before, immediately, one month and two months after intervention and score Domestic violence will be measured using a standard questionnaire to measure violence against women before, one month and two months after the intervention. Intervention 2: Control group: There is no intervention in the control group. after completing the training resilience score and coping style score using Connor and Davidson resilience scale (CD-RISC) and Lazarus and Folkman's coping style questionnaire (WOCQ) before, immediately, one month and two months after intervention and score Domestic violence will be measured using a standard questionnaire to measure violence against women before, one month and two months after the intervention. Educational Contents in the form of educational pamphlets will be provided to them after the 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>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 more information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Dr.Zahra Boroumandfar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Hezar Jerib street</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8175845491</zip>
        <telephone>+98 31 3625 1726</telephone>
        <email>boroumandfar@nm.mui.ac.ir</email>
        <affiliation>Esfahan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Zahra Boroumandfar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences and Health Services, Hezar Jerib street</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8175845491</zip>
        <telephone>+98 31 3625 1726</telephone>
        <email>boroumandfar@nm.mui.ac.ir</email>
        <affiliation>Esfahan 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>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Experience exposure to one type of physical, psychological, sexual violence
Willingness to participate in the study.
Having lived with your spouse for at least one year
Have a minimum literacy
No severe mental illness registered in the apple system.
No pregnancy
No drug abuse
No chronic debilitating physical illness</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Unwillingness of a person to continue participating in research
Absence from two sessions of training classes</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
      <hc_code></hc_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
      <hc_keyword></hc_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>Intervention group: The intervention group is divided into two groups of 16 people and each of them will be given a Meichenbaum self-study group training in 7 sessions of 60 minutes in a two-month course. self-study is a technique of the CBT approach that is an exercise to improve self-control and self-talk is used to stimulate and reinforce during treatment. The self-study technique uses positive verbal expressions to reduce negative thoughts and to increase self-control through the mind. The most important step in the self-learning technique is that the person begins to speak slowly in their heart. after completing the training resilience score and coping style score using Connor and Davidson resilience scale (CD-RISC) and Lazarus and Folkman's coping style questionnaire (WOCQ) before, immediately, one month and two months after intervention and score Domestic violence will be measured using a standard questionnaire to measure violence against women before, one month and two months after the intervention.</i_keyword>
      <i_keyword>Control group: There is no intervention in the control group. after completing the training resilience score and coping style score using Connor and Davidson resilience scale (CD-RISC) and Lazarus and Folkman's coping style questionnaire (WOCQ) before, immediately, one month and two months after intervention and score Domestic violence will be measured using a standard questionnaire to measure violence against women before, one month and two months after the intervention. Educational Contents in the form of educational pamphlets will be provided to them after the completion of the research.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Resilience score. Timepoint: Before, immediately, one month and two months after the intervention. Method of measurement: Demographic Questionnaire, Standard Violence Against Women Questionnaire, Connor &amp; Davidson Resilience Questionnaire and Coping Styles Questionnaire.</prim_outcome>
      <prim_outcome>Coping styles score. Timepoint: Before, immediately, one month and two months after the intervention. Method of measurement: Coping Styles Questionnaire( WOCQ).</prim_outcome>
      <prim_outcome>Domestic violence. Timepoint: Before, one month and two months after the intervention. Method of measurement: Standard Questionnaire for Measuring Violence Against Women.</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>Esfahan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-04-04</approval_date>
        <contact_name>Ethics Committee of the faculty of Nursing, Management and Rehabilitation - Isfahan University of Me</contact_name>
        <contact_address>Isfahan University of Medical Sciences and Health Services, Hezar Jerib street Isfahan Isfehan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
