<?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>IRCT20210126050145N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-04-15</date_registration>
      <primary_sponsor>The University of Farhangian</primary_sponsor>
      <public_title>effect of  endurance training on buffering system</public_title>
      <acronym></acronym>
      <scientific_title>The effect of 8 weeks endurance training on buffering system and the results of three different types of recovery</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-04-09</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/53945</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Basic scienece, Randomization description: First of all, among the students of Farhangian University of Hamadan, Students who meet the inclusion criteria, a sample is selected according to the sampling method and based on balance block randomization method will be placed in active recovery group (A), Passive recovery group (B) and stretching recovery group (C). For this purpose, six sheets of paper are provided by the researcher, writing on two sheets “A” for “first” and on two “B” for “second” and on another two “C” for third. The paper sheets will be pooled, placed in a container, and randomly will be drawn one at a time for each student without replacement until all six sheets are drawn. Then, the six paper sheets will be placed back into the container and this action will be repeated until the sample size is reached.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Effect.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group 1: After introducing the study and stating its goals, 30 students who have been selected as a sample fill out the consent form and are divided into three groups of 10 people. At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with active recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly. Intervention 2: Intervention group 2: At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with passive recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly. Intervention 3: Intervention group 3: At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with Stretching recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly.</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>Undecided - It is not yet known if there will be a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for indecision in sharing IPD is There is no more information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mahtab Tavakoli</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>NO 2 , Besat alley ,Rokni Ave ,  Hamedan</address>
        <city>Hamedan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6516796913</zip>
        <telephone>+98 81 3823 9552</telephone>
        <email>tavakoli.mahtab20@yahoo.com</email>
        <affiliation>The University of Farhangian</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Seyed Mohammad Marandi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University ,Azadi square ,Isfahan</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8174673441</zip>
        <telephone>+98 31 3793 2640</telephone>
        <email>smmarandi2001@yahoo.com</email>
        <affiliation>The University of Isfahan</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Student of first year</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Being an athlete</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>Other</i_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group 1: After introducing the study and stating its goals, 30 students who have been selected as a sample fill out the consent form and are divided into three groups of 10 people. At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with active recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly.</i_keyword>
      <i_keyword>Intervention group 2: At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with passive recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly.</i_keyword>
      <i_keyword>Intervention group 3: At first, blood samples were taken from 10 samples of this group and after Intense repetitive endurance training test with Stretching recovery, blood samples were taken again. Then intense endurance training is performed for 8 weeks and three sessions a week, and the stages of Intense repetitive endurance training testing and blood sampling are performed exactly.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>PH. Timepoint: Before  and after  endurance training. Method of measurement: Arterial blood draw.</prim_outcome>
      <prim_outcome>HCO3-. Timepoint: Before  and after  endurance training. Method of measurement: Arterial blood draw.</prim_outcome>
      <prim_outcome>O2SAT. Timepoint: Before  and after  endurance training. Method of measurement: Arterial blood draw.</prim_outcome>
      <prim_outcome>BE. Timepoint: Before  and after  endurance training. Method of measurement: Arterial blood draw.</prim_outcome>
      <prim_outcome>PCO2. Timepoint: Before  and after  endurance training. Method of measurement: Arterial blood draw.</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>The University of Farhangian</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-12-04</approval_date>
        <contact_name>Isfahan university ethics committee</contact_name>
        <contact_address>Department of exercise physiology, sport science faculty, Isfahan University. Isfahan, Iran. Isfahan Isfehan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
