<?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>IRCT20201031049202N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-11-13</date_registration>
      <primary_sponsor>Allameh Hospital</primary_sponsor>
      <public_title>Effect of a period of combined training on Leptin, Adiponectin, and Resistin in Middle-aged men after Coronary artery bypass surgery (CABG)</public_title>
      <acronym></acronym>
      <scientific_title>Effect of a period of combined training on Leptin, Adiponectin and Resistin in Middle-aged men after Coronary artery bypass surgery (CABG(</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2020-10-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>26</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/51959</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Supportive.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Coronary artery bypass graft patients.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Rehabilitation program (aerobic, resistance training),26 men who undergone bypass surgeries in the 40-60 age range, and by available sampling method will be selected, and randomly they were categorized into two groups.14 individuals experimental group. Participants as an experimental group in the rehabilitation center of Javadalameh Heart Hospital completed exercises and In order to reduce the mediator and mixer effect in research, according to aspects of control the short-term effects of the diet based on the desired indicators, in this session, the doctor recommended eating ready meals at least 24 hours before exercise program and blood sampling. they avoided caffeinating beverages and similar diets. Thus, 14 people (combined exercise group) be selected. Examples in the same environment and conditions have performed combined sports activities. Intervention 2: Control group: (Patients without rehabilitation program):26 men who undergone bypass surgeries in the 40-60 age range, and by available sampling method will be selected, and randomly they were categorized into two groups.12 individuals control group, the control group included those who person that didn't participate in the cardiac rehabilitation program after surgery and haven't any regular physical activity and In order to reduce the mediator and mixer effect in research, according to aspects of control the short-term effects of the diet based on the desired indicators, in this session, the doctor recommended eating ready meals at least 24 hours before exercise program and blood sampling. they avoided caffeinating beverages and similar diets. Thus,12 people (control group) be selected. Examples in the same environment and conditions have performed combined sports activities.</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:
some sections of results about some information on the main outcome can be shared.

When:
the access time is period from 1399 onwards

To whom:
Only supervisors and advisors

Conditions:
for use, it must be coordinated with supervisors, consultants, and researchers

Where to obtain:
Hossein Nikkar
h.nikkar@iau-neyshabur.ac.ir
09151601391
Dr. Amir Rashidlamir
amir.rashidlamir@gmail.com 
09151514174

How to obtain:
First, the request should be given to the supervisors and advisors. After their approval, the data will be assigned.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Dr. Amir Rashidlamir</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Azadi Square, Ferdowsi University, Mashhad,Razavi khorasan province, Iran</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9177948974</zip>
        <telephone>+98 51 3880 5000</telephone>
        <email>amir.rashidlamir@gmail.com</email>
        <affiliation>Ferdowsi University of Mashhad</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Amir Rashid Lamir</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Azadi Square, Ferdowsi University, Razavi khorasan province, Mashhad, Iran</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9177948974</zip>
        <telephone>+98 51 3880 5000</telephone>
        <email>amir.rashidlamir@gmail.com</email>
        <affiliation>Ferdowsi University of Mashhad</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>In the 40-60 age range
Being interested to participate in research
Hearing, cognitive and visual health
systolic blood pressure higher than 160 mmHg and diastolic blood pressure higher than 100 mmHg
Lack of suffering from acute and specific diseases that prevent doing exercises
The subjects who were taking the same medications
Not use of neurological medications
Not use of aid equipment to walk e.g by cane and walker</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>60 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>Cardiac arrhythmia
o be observed Myocardial Infarction in the ECG during training sessions
respiratory disorders during rehabilitation and training
unstable angina</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Rehabilitation program (aerobic, resistance training),26 men who undergone bypass surgeries in the 40-60 age range, and by available sampling method will be selected, and randomly they were categorized into two groups.14 individuals experimental group. Participants as an experimental group in the rehabilitation center of Javadalameh Heart Hospital completed exercises and In order to reduce the mediator and mixer effect in research, according to aspects of control the short-term effects of the diet based on the desired indicators, in this session, the doctor recommended eating ready meals at least 24 hours before exercise program and blood sampling. they avoided caffeinating beverages and similar diets. Thus, 14 people (combined exercise group) be selected. Examples in the same environment and conditions have performed combined sports activities.</i_keyword>
      <i_keyword>Control group: (Patients without rehabilitation program):26 men who undergone bypass surgeries in the 40-60 age range, and by available sampling method will be selected, and randomly they were categorized into two groups.12 individuals control group, the control group included those who person that didn't participate in the cardiac rehabilitation program after surgery and haven't any regular physical activity and In order to reduce the mediator and mixer effect in research, according to aspects of control the short-term effects of the diet based on the desired indicators, in this session, the doctor recommended eating ready meals at least 24 hours before exercise program and blood sampling. they avoided caffeinating beverages and similar diets. Thus,12 people (control group) be selected. Examples in the same environment and conditions have performed combined sports activities.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Percentage of people who underwent coronary artery bypass grafting. Timepoint: before cardiac rehabilitation period and end of it. Method of measurement: Patients ECG, condition of physical fitness, Cardiovascular and Ejection Fraction (EF) risk factors, the Rehabilitation program results.</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>Allameh Hospital</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2020-09-24</approval_date>
        <contact_name>thics committee of Islamic Azad University, Neyshabur Branch</contact_name>
        <contact_address>Research Blvd., Islamic Azad University , Neyshabour Branch, Neyshabour, Khorasan Province, Iran Neyshabur Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
