<?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>IRCT2016050827697N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2017-05-31</date_registration>
      <primary_sponsor>Research administation of Zahedan University of Medical Sciences</primary_sponsor>
      <public_title>Cardiac rehabilitation program in patients after CABG</public_title>
      <acronym>CABG</acronym>
      <scientific_title>The efficacy of comprehensive cardiac rehabilitation program based on exercise and psychological interventions on illness perception, quality of relationships, self efficacy, psychological distress in patients with coronary artery bypass surgery (CABG).</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2013-01-29</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/22636</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Health service research.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Other Physical Therapy Therapeutic Procedures.</hc_freetext>
      <i_freetext>The experiment was pretest-posttest and had no control group. The study was conducted in cardiac rehabilitation center of Tehran Heart Hospital. For this purpose, among cardiovascular patients of Tehran Heart Center, who referred to Rehabilitation Clinic of Tehran Heart Center hospital one month after bypass surgery during the study period, 120 subjects were randomly selected. Subjects of the sample group  were assessed in two pre-test and post-test steps (two months after the start of intervention and at the end of rehabilitation program) using illness perception questionnaire (BIPS), relationship quality questionnaire (QRI), cardiac patients self efficacy scale (CSQ), and depression, anxiety, and stress scale (psychological distress) (DASS-21). Participants were given rehabilitation program (physical / psychological) during 24 sessions (8 weeks), 3 days per week assigned to exercise training, 6 sessions assigned to psychological trainings, and on session (the last session) was held for health tour..</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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Dinpajouh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Department of Nursing., Alborz University of Medical Science., Eshteraki St., Baghestan Blv</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 26343360079</telephone>
        <email>f.dinpajouh@abzums.ac.irf.dinpajouh@gmail.com</email>
        <affiliation>Alborz University of Medical Science</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fatemeh Dinpajouh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Department of Nursing., Alborz University of Medical Science., Eshteraki St., Baghestan Blv</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 26343360079</telephone>
        <email>f.dinpajouh@abzums.ac.irf.dinpajouh@gmail.com</email>
        <affiliation>Alborz University Of Medical Saiences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Study population: among cardiovascular patients of Tehran Heart Center, who referred to Rehabilitation Clinic of Tehran Heart Center hospital one month after bypass surgery and selected by inclusion and exclusion criteria. Inclusion criterion: having at least education level of primary school; age 40 to 65 years old; one month after the first time of  CABG in Tehran Heart Center; lack of mental illnesses; lack of serious medical problems such as diabetes uncontrolled, sharp decline in left ventricular function, and other chronic diseases other than heart disease; lack of Disability, written informed consent.</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>93.36</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Cardiac retraining</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>The experiment was pretest-posttest and had no control group. The study was conducted in cardiac rehabilitation center of Tehran Heart Hospital. For this purpose, among cardiovascular patients of Tehran Heart Center, who referred to Rehabilitation Clinic of Tehran Heart Center hospital one month after bypass surgery during the study period, 120 subjects were randomly selected. Subjects of the sample group  were assessed in two pre-test and post-test steps (two months after the start of intervention and at the end of rehabilitation program) using illness perception questionnaire (BIPS), relationship quality questionnaire (QRI), cardiac patients self efficacy scale (CSQ), and depression, anxiety, and stress scale (psychological distress) (DASS-21). Participants were given rehabilitation program (physical / psychological) during 24 sessions (8 weeks), 3 days per week assigned to exercise training, 6 sessions assigned to psychological trainings, and on session (the last session) was held for health tour.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Quality of relationships. Timepoint: Before intervention, immediately after the interventions. Method of measurement: QRI Questionnaire.</prim_outcome>
      <prim_outcome>Illness perception. Timepoint: Before intervention, immediately after the interventions. Method of measurement: BIPS Quetionnaire.</prim_outcome>
      <prim_outcome>Self efficiency. Timepoint: Before intervention, immediately after the interventions. Method of measurement: CSEQ Quetionnaire.</prim_outcome>
      <prim_outcome>Depression, anxiety, stress. Timepoint: Before intervention, immediately after the interventions. Method of measurement: DASS Quetionnaire.</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>Research administation of Zahedan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2012-07-19</approval_date>
        <contact_name>Zahedan Univrsity of Medical Sciences</contact_name>
        <contact_address>Zahedan University of Medical Sciences, Khalije Fars Highway Zahedan  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
