<?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>IRCT20180707040373N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-07-17</date_registration>
      <primary_sponsor>Semnan University- Faculty of psychology and education</primary_sponsor>
      <public_title>The impact of eye movement desensitization and reprocessing and progressive counting on CABG</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of the efficacy of eye movement desensitization and reprocessing procedure and progressive counting technique on anxiety, depression, stress and quality of life in patients undergone coronary artery bypass graft surgery</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-07-11</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/32368</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention, Randomization description: In this research participants will be selected using a random sampling method. Participants will be assigned to each groups after matching them based on their age and gender and designating each one of them numbers from 1 to 60. Subsequently, using the  Random Number Selection software each participant will be randomly assigned to one of the groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>coronary artery bypass graft surgery.</hc_freetext>
      <i_freetext>Intervention 1: The present study includes 2 types of intervention: 1) Eye Movement Desensitization and Reprocessing; 2) Progressive Counting; and 3) a control group.First, a pretest will be obtained from all 3 groups. Then, intervention that include 6 sessions will be carried out in the 2 experimental groups. Finally, a post test will be taken from all 3 groups. Subsequently, after six months a follow up evaluation will be taken from all three groups. Intervention 2: Intervention group: Intervention group 2, progressive counting. Progressive counting is a new method of resolving trauma. In this method, the therapist uses progressive counting (1 to 10, then 1 to 20, and so to 100), and at the same time asks client to do the imagination on a traumatic event from the beginning to the end to treat his/her traumatic memory. Intervention 3: Control group: No intervention, only as 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:
Research findings will be published in scientific journals.

When:
The documentation and research results are likely to be published in 2018-2019.

To whom:
The full research document will be available in Semnan University, faculty of Psychology and education. Research results will be available to researchers as an article and book.

Conditions:
Using the results of the study, mentioning the number of participants in the study, the type of population and the research sample, as well as mentioning the interventions allowed.

Where to obtain:
Semnan University, faculty of psychology and education, Information and Documentation Center of Iran (IranDoc) Or sending a message to researcher: mrbidhendi@yahoo.com

How to obtain:
Visiting the Irandoc center or Semnan University Library Or one week after sending email to the writer

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mohammad Reza Abdoli Bidhendi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No 15, Vahid-e- gharbi alley, Kokab st., Sattarkhan st., Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1441993813</zip>
        <telephone>+98 21 6643 8583</telephone>
        <email>mrbidhendi@semnan.ac.ir</email>
        <affiliation>Faculty of psychology and education- Semnan University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Parvin Rafieinia</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Mahdishahr, Faculty of psychology and education, Semnan University</address>
        <city>Semnan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3564111156</zip>
        <telephone>+98 23 3362 4250</telephone>
        <email>p_rafieinia@semnan.ac.ir</email>
        <affiliation>Semnan University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>The sample population included patients undergone coronary artery bypass graft surgery who were candidates for cardiac rehabilitation 4 to 6 weeks after surgery.
Patients undergone coronary artery bypass grafting that score 24 and above on impact of events scale- revised
Not receiving any psychological treatment or counseling before intervention period</inclusion_criteria>
      <agemin>30 months</agemin>
      <agemax>60 months</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having sustained angina pectoris, acute phase of myocardial infarction and unstable arrhythmia
Education less than diploma
Not receiving any psychological treatment or counseling during the intervention period</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>I25</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Chronic ischemic heart disease</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>The present study includes 2 types of intervention: 1) Eye Movement Desensitization and Reprocessing; 2) Progressive Counting; and 3) a control group.First, a pretest will be obtained from all 3 groups. Then, intervention that include 6 sessions will be carried out in the 2 experimental groups. Finally, a post test will be taken from all 3 groups. Subsequently, after six months a follow up evaluation will be taken from all three groups.</i_keyword>
      <i_keyword>Intervention group: Intervention group 2, progressive counting. Progressive counting is a new method of resolving trauma. In this method, the therapist uses progressive counting (1 to 10, then 1 to 20, and so to 100), and at the same time asks client to do the imagination on a traumatic event from the beginning to the end to treat his/her traumatic memory.</i_keyword>
      <i_keyword>Control group: No intervention, only as control group</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Emotional signs. Timepoint: Before and after of Intervention. Method of measurement: Depression Anxiety Stress Scales (DASS-21).</prim_outcome>
      <prim_outcome>Quality Of Life. Timepoint: Before and after of Intervention. Method of measurement: World Health Organization's Quality Of Life questionnaire (WHOQOL-BREF).</prim_outcome>
      <prim_outcome>Signs of Post Traumatic Stress. Timepoint: Before and after of Intervention. Method of measurement: Impact of Event Scale - Revised.</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>Semnan University- Faculty of psychology and education</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-06-12</approval_date>
        <contact_name>Ethics committee of Semnan University of Medical Science</contact_name>
        <contact_address>Mahdishahr ;Education and psychology faculty of semnan university Semnan Semnan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
