<?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>IRCT201103146059N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2011-12-20</date_registration>
      <primary_sponsor>Kashan University of Medical Sciences</primary_sponsor>
      <public_title>Effects of cardiac rehabilitation in ischemic heart diseases</public_title>
      <acronym></acronym>
      <scientific_title>Survey of the effect of cardiac rehabilitation program on clinical and paraclinical findings of patients with ischemic heart disease</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2010-10-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>200</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/6515</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Ischaemic heart disease.</hc_freetext>
      <i_freetext>Intervention 1: Intervention Group, in addition to routine treatment programs, also receive rehabilitation programs the results of clinical and paraclinical findings will be recorded.A  cardiologist examine patients in rehabilitation sessions, and their clinical symptoms are recorded by medical student. At the same time for Para clinical studies, 10cc , fasting blood was taken with the consent of the patient and sent to the laboratory.This is done in two sessions (pre-rehabilitation program and at the end of an 8-week rehabilitation program). Rehabilitation program include, a three-week aerobic exercise session, 2 sessions of training - is consulting. Exercise sessions  included 50 minutes warm-up, isometric exercises for 30 minutes, and 10 minutes cooling down. Training sessions include nutrition education, lifestyle modification, , weight loss, exercise in everyday activities, avoid heavy activity that can lead to fatigue and shortness of breath. Learning how to keep control of vital signs, including pulse, blood pressure, avoid extreme heat and cold, proper diet, limit salt and alcohol and fat consumption, To encourage  consumption of fresh vegetables and fruit, and cereal fiber consumption, quit smoking and alcohol.Also investigate and resolve the problems they cause. Intervention 2: Control group: routine treatment programs receive.Include all control program except Exercise sessions.</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>Hasasn Rajabi Moghadam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Beheshti Hospital-Kashan</address>
        <city>Kashan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 36 1555 0026</telephone>
        <email>rajabi_ha@kaums.ac.ir</email>
        <affiliation>Kashan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fariba Raygan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Beheshti Hospital,Ravandi Blvd,Kashan</address>
        <city>Kashan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 36 1555 0026</telephone>
        <email>dr.alireza_hosseini@yahoo.com</email>
        <affiliation>Kashan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: Ischemic heart disease;Physically ability to do exercise test.&#13;
&#13;
Exclusion criteria: Less than 4 weeks from ischemic heart diagnosis; Heart failure ; Sever hypertension; Arrhythmia.</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>I25.8</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Other forms of chronic ischaemic heart disease</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention Group, in addition to routine treatment programs, also receive rehabilitation programs the results of clinical and paraclinical findings will be recorded.A  cardiologist examine patients in rehabilitation sessions, and their clinical symptoms are recorded by medical student. At the same time for Para clinical studies, 10cc , fasting blood was taken with the consent of the patient and sent to the laboratory.This is done in two sessions (pre-rehabilitation program and at the end of an 8-week rehabilitation program). Rehabilitation program include, a three-week aerobic exercise session, 2 sessions of training - is consulting. Exercise sessions  included 50 minutes warm-up, isometric exercises for 30 minutes, and 10 minutes cooling down. Training sessions include nutrition education, lifestyle modification, , weight loss, exercise in everyday activities, avoid heavy activity that can lead to fatigue and shortness of breath. Learning how to keep control of vital signs, including pulse, blood pressure, avoid extreme heat and cold, proper diet, limit salt and alcohol and fat consumption, To encourage  consumption of fresh vegetables and fruit, and cereal fiber consumption, quit smoking and alcohol.Also investigate and resolve the problems they cause.</i_keyword>
      <i_keyword>Control group: routine treatment programs receive.Include all control program except Exercise sessions.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Duration of chest pain. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: Questionnaire.</prim_outcome>
      <prim_outcome>Systolic blood pressure at rest. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: Per mm Hg using a mercury barometer.</prim_outcome>
      <prim_outcome>Diastolic blood pressure at rest. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: Per mm Hg using a mercury barometer.</prim_outcome>
      <prim_outcome>Exercise Tolerance. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: Duration of exercise Per minute.</prim_outcome>
      <prim_outcome>Maximum oxygen consumption. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: exercise tolerance test per METS.</prim_outcome>
      <prim_outcome>Cholesterol. Timepoint: Before and after cardiac rehabilitation program. Method of measurement: Per mg / dl.</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>Kashan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2008-09-16</approval_date>
        <contact_name>Kashan University of Medical Sciences</contact_name>
        <contact_address>111 / 87155, Ravandi Blvd  ,Kashan Kashan  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
