<?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>IRCT20191019045152N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-12-29</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>Effect of Core Stabilization Exercises on Physiological and Functional Characteristic of Athletes</public_title>
      <acronym></acronym>
      <scientific_title>Effect of Core Stabilization Exercises on Selected Physiological and Functional Characteristic of Paddlers</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-09-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>24</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/43983</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Other, Randomization description: Simple randomization - lottery: in which the researcher puts people in different groups based on the lottery and the lottery is done in the form of registration on sheets with a black background, Blinding description: In this study, the researcher and supervisor were blinded by the study and were unaware of the study groups. So that only the coaches hired and the subjects who received the activity were inevitably aware of the type of sports intervention. In this study, to prevent the researcher from biasing in the analysis of the results until the last stage of the study, which was the analysis of the findings, the researcher was unaware of the grouping process. It should be noted that the participants were not blinded because they were doing the exercise. In fact, it was not possible for the participants to be blinded because they understood and performed the exercise.</study_design>
      <phase>N/A</phase>
      <hc_freetext>The effect of trunk stability exercises on performance and physiological factors of athletes.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: 8 weeks of torso stability training with resistance training (3 days / week, 40 minutes of training: 20 minutes of resistance training (with intensity of 70 to 80% 1RM and 6-8 repetitions, 3 sets); torso stability training for 20 minutes with Intensity of 70-80% of a maximum repetition was done in 12 to 8 repetitions and included trunk stability exercises to strengthen the abdominal, lower pelvic, transverse abdominal and diaphragm muscles, as well as trunk stability exercises to strengthen the shoulder girdle, hamstring, serine and all muscles. The pelvic floor muscles were the lower back and straighteners of the dorsal vertebrae. Intervention 2: Control group: 8 weeks of resistance training (3 days / week, 40 minutes of training: with intensity of 70 to 80% 1RM and 6-8 repetitions, 3 sets).</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 of the data, including information about the main consequences, can be shared

When:
Access period starts 3 months after printing

To whom:
Researchers, professors in this field

Conditions:
The data is unidentifiable individual
Will only be presented if compared to their research data

Where to obtain:
Faegheh Naghizadeh

How to obtain:
Describe the request and method of study and the title of the research in the form of an email and clearly state the reasons for the need for the data.

Comments:
mail to : faegheh.naghizadeh@srbiau.ac.ir</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Faegheh Naghizadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>First Floor, No. 10, Yas Square, Jahan Nama Town, Tehran-Karaj highway</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3159846711</zip>
        <telephone>+98 26 3230 5954</telephone>
        <email>faegheh.naghizadeh@srbiau.ac.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Faegheh Naghizadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>First Floor, No. 10, Yas Square, Jahan Nama Town, Tehran-Karaj highway</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3159846711</zip>
        <telephone>+98 26 3230 5954</telephone>
        <email>faegheh.naghizadeh@srbiau.ac.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Adult girls 12 to 13 years
Be Athlete and kayak girls
Having Physical and mental health
They don't do any other exercise
Have no other special diet
Teenage kayak girls at Azadi Sport Complex</inclusion_criteria>
      <agemin>12 years</agemin>
      <agemax>13 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Lack of interest in participating in the project
Inability to attend regular training sessions</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>N/A</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: 8 weeks of torso stability training with resistance training (3 days / week, 40 minutes of training: 20 minutes of resistance training (with intensity of 70 to 80% 1RM and 6-8 repetitions, 3 sets); torso stability training for 20 minutes with Intensity of 70-80% of a maximum repetition was done in 12 to 8 repetitions and included trunk stability exercises to strengthen the abdominal, lower pelvic, transverse abdominal and diaphragm muscles, as well as trunk stability exercises to strengthen the shoulder girdle, hamstring, serine and all muscles. The pelvic floor muscles were the lower back and straighteners of the dorsal vertebrae.</i_keyword>
      <i_keyword>Control group: 8 weeks of resistance training (3 days / week, 40 minutes of training: with intensity of 70 to 80% 1RM and 6-8 repetitions, 3 sets).</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Blood lactate dehydrogenase. Timepoint: The first at the beginning of the study (before the intervention) and the second after 8 weeks of practice (end of the intervention). Method of measurement: lactate dehydrogenase kit.</prim_outcome>
      <prim_outcome>VO2max of rowers. Timepoint: The first at the beginning of the study (before the intervention) and the second after 8 weeks of Training (end of the intervention). Method of measurement: Step Test for Womens.</prim_outcome>
      <prim_outcome>The record level of 500 meters. Timepoint: The first at the beginning of the study (before the intervention) and the second after 8 weeks of Training (end of the intervention). Method of measurement: 500m rowing test.</prim_outcome>
      <prim_outcome>The functional level of the trunk. Timepoint: The first at the beginning of the study (before the intervention) and the second after 8 weeks of Training (end of the intervention). Method of measurement: Body Composition (inbody).</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>Islamic Azad University Science and Research Branch</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-10-17</approval_date>
        <contact_name>Ethics Committee in Biomedical Research of Ministry of Islamic Azad University Science and Research </contact_name>
        <contact_address>Floor 13, Block A, Ministry of Health &amp; Medical Education Headquarters, Between Zarafashan &amp; South Falamak, Qods Town, Tehran, Iran. Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
