<?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>IRCT2014121012551N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2015-01-02</date_registration>
      <primary_sponsor>Isfahan University of Medical Sciences</primary_sponsor>
      <public_title>The effect of resistance exercise on lipid profile</public_title>
      <acronym></acronym>
      <scientific_title>The effect of resistance exercise on lipid profile in coronary artery disease patients:a clinical randomized trial</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2013-04-08</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>40</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/12604</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention.</study_design>
      <phase>N/A</phase>
      <hc_freetext>coronary artery disease.</hc_freetext>
      <i_freetext>Intervention 1: Intervention was conducted in the form of 45-–60 minute sessions, twice a week[12] (8-–12 AM) for eight 8 weeks in the rehabilitation unit of the cardiovascular research center.In the study group, in addition to aerobic exercises, resistance exercise was also administrated performed. In the first session, to determine the weight, the target weight was determined based on the heaviest weight each subject could lift for 12-–15 times in the expected range of motion. In all sessions, there were warm warm-up, exercise, and cool cool-down stages. Warm Warm-up and cool cool-down stages were conducted by with stretching exercises for 10-–15 min.&#13;
The exercise included resistance exercise that was administrated performed for 20-–25 min, in addition to aerobic exercise. Resistance exercise was administrated performed by use of light weights in the range of motion of the elbow, shoulder, and knee joints. The number of repetitions in the range of motion was initially considered 10, and then, was gradually increased to 15. After the end of each set with 15 repetitions, the weight was increased by 3-–5% . In the second session, each subject held his/ her target weight in hand and administrated performed one set of side lateral, front, and overhead raise, overhead triceps extensions, alternating biceps curls and shoulder press, and weight squad with 10 repetitions. In the sessions 3-–7, a set of the above – -mentioned exercises were was repeated for 11 - 15 repetitions, respectively. In the 8th session, both the number of the sets and the weight were increased (by 3-–5% of the previous weight) in such a way that two sets of the above – -mentioned exercises were administrated performed by with 10 repetitions, with a rest period of one min between the sets. In sessions 9-–13, two sets of the above resistance exercises were administrated performed with 11 and 15 repetitions in each session, respectively, and a one  minute rest period between the sets. In session 14, the number of the sets and the weight were increased again, . and in sessions 15-–16, three sets with repetitions of 11-–12 times were administrate dperformed. Intervention 2: Control group  was conducted in the form of 45-–60 minute sessions, twice a week (8-–12 AM) for eight 8 weeks in the rehabilitation unit of the cardiovascular research center. Subjects in the control group just attended in a routine exercise session of in the rehabilitation unit in of the cardiovascular research center, which included running or treadmill with an average speed of 4four km/hr and cycling on a stationary bicycle for 15 min.</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>Zahra Salehi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Hezar Jerib Avenuse, Isfahan</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 31 3792 2935</telephone>
        <email>z_salehi@nm.mui.ac.ir</email>
        <affiliation>Isfahan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Zahra Salehi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Hezar Jerib Avenuse, Isfahan</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 31 3792 2935</telephone>
        <email>z_salehi@nm.mui.ac.ir</email>
        <affiliation>Isfahan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>inclusion criteria    :    Having coronary arteries’ involvement diagnosed by angiography ;  two  months after  myocardial infarction (MI);10 days after coronary artery angioplasty;  three months  after coronary by- pass surgery.&#13;
Exclusion criteria : Playing an athletic sport;  being absent for more than three sequential sessions in the rehabilitation program; incidence of severe health problems</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>I25.1</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Atherosclerotic 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 was conducted in the form of 45-–60 minute sessions, twice a week[12] (8-–12 AM) for eight 8 weeks in the rehabilitation unit of the cardiovascular research center.In the study group, in addition to aerobic exercises, resistance exercise was also administrated performed. In the first session, to determine the weight, the target weight was determined based on the heaviest weight each subject could lift for 12-–15 times in the expected range of motion. In all sessions, there were warm warm-up, exercise, and cool cool-down stages. Warm Warm-up and cool cool-down stages were conducted by with stretching exercises for 10-–15 min.&#13;
The exercise included resistance exercise that was administrated performed for 20-–25 min, in addition to aerobic exercise. Resistance exercise was administrated performed by use of light weights in the range of motion of the elbow, shoulder, and knee joints. The number of repetitions in the range of motion was initially considered 10, and then, was gradually increased to 15. After the end of each set with 15 repetitions, the weight was increased by 3-–5% . In the second session, each subject held his/ her target weight in hand and administrated performed one set of side lateral, front, and overhead raise, overhead triceps extensions, alternating biceps curls and shoulder press, and weight squad with 10 repetitions. In the sessions 3-–7, a set of the above – -mentioned exercises were was repeated for 11 - 15 repetitions, respectively. In the 8th session, both the number of the sets and the weight were increased (by 3-–5% of the previous weight) in such a way that two sets of the above – -mentioned exercises were administrated performed by with 10 repetitions, with a rest period of one min between the sets. In sessions 9-–13, two sets of the above resistance exercises were administrated performed with 11 and 15 repetitions in each session, respectively, and a one  minute rest period between the sets. In session 14, the number of the sets and the weight were increased again, . and in sessions 15-–16, three sets with repetitions of 11-–12 times were administrate dperformed.</i_keyword>
      <i_keyword>Control group  was conducted in the form of 45-–60 minute sessions, twice a week (8-–12 AM) for eight 8 weeks in the rehabilitation unit of the cardiovascular research center. Subjects in the control group just attended in a routine exercise session of in the rehabilitation unit in of the cardiovascular research center, which included running or treadmill with an average speed of 4four km/hr and cycling on a stationary bicycle for 15 min</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Lipid Profile. Timepoint: Before, After and 4 weeks after the end of the intervention. Method of measurement: Mg. Laboratory test.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Blood Sugar. Timepoint: Before, After and 4 weeks after the end of the intervention. Method of measurement: Mg,Laboratory test.</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>Isfahan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2013-03-02</approval_date>
        <contact_name>Isfahan University of Medical Sciences</contact_name>
        <contact_address>Isfahan University of Medical Sciences, Hezar Jerib Avenuse, Isfahan Isfahan  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
