<?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>IRCT20180626040244N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-11-21</date_registration>
      <primary_sponsor>Allameh Tabataba'i University</primary_sponsor>
      <public_title>effects of 6-week corrective-plyometric training with and without visual feedback on dynamic knee valgus</public_title>
      <acronym></acronym>
      <scientific_title>effects of 6-week corrective-plyometric training with and without visual feedback on lower extremity Biomechanics and dynamic balance in junior female athletes with dynamic knee valgus</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2020-10-13</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>26</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/51244</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention, Randomization description: After screening,  by simple randomization participants will be divided into 3 groups of control (8 participants), exercise (8 participants), and feedback (10 participants). The randomization is going to be done by random numbers chart, by considering numbers between 0 to 8 for control group, 8 to 16 for exercise group, and 16 to 26 for feedback group. The researcher will choose one of the numbers and move through a previously determined direction and register the number and give it to the related group, Blinding description: In this study, the assessor (who is the researcher) is blinded to the participants' information (single blinding), and the results of participants tests are analyzed based on participants' given number and without knowing their names. That information includes participants names, and weight, height, and age information.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Dynamic knee valgus.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group 1: This group will practice 6 weeks of plyometric-exercises with visual feedback during the exercises from a mirror in a sports gym. Each week includes 3 sessions of practice which takes 30 minutes. Exercises include squats, balance training, and jump-landing exercises. Intervention 2: Intervention group 2: This group will practice 6 weeks of plyometric-exercises without any visual feedback during the exercises, in a sports gym. Each week includes 3 sessions of practice which takes 30 minutes. Exercises include squats, balance training, and jump-landing exercises. Intervention 3: Control group: This group will not receive any exercises from the assessor and continues their daily routine 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:
After publication, the data which will be also presented in the article, will be given to the researchers in Excel format which includes the pre and post interventions' results of landing tests' biomechanical analysis and dynamic balance, for future studies like meta-analysis studies.

When:
After publication

To whom:
The published data of the current study will be accessible for the researchers in the academic institutes and universities, and also people who work in the industry.

Conditions:
After publishing the article, the data will be used in future researches, like meta-analysis or other types of researches.

Where to obtain:
Responding author

How to obtain:
Sending via an email

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Rahman Sheikh Hoseini</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>West Azadi sports complex entrance, Hakim highway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۱۴۸۵۷۴۳۴۱۱</zip>
        <telephone>+98 21 4411 8629</telephone>
        <email>rahmanhoseini@atu.ac.ir</email>
        <affiliation>Allameh Tabatabai University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Rahman Sheikh Hoseini</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>West Azadi sports complex entrance, Hakim highway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۱۴۸۵۷۴۳۴۱۱</zip>
        <telephone>+98 21 4411 8629</telephone>
        <email>rahmanhoseini@atu.ac.ir</email>
        <affiliation>Allameh Tabatabai University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Observing dynamic knee valgus by performing single leg squat test
Regular physical activity between 3 to 5 years</inclusion_criteria>
      <agemin>10 years</agemin>
      <agemax>14 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>suffering from spine or lower extremity disorders
history of fracture, sprain, or strain in lower extremity
history of spine or lower extremity surgery
using any medicine or painkiller</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M21.06</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Valgus deformity, not elsewhere classified, knee</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Prevention</i_code>
      <i_code>Prevention</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group 1: This group will practice 6 weeks of plyometric-exercises with visual feedback during the exercises from a mirror in a sports gym. Each week includes 3 sessions of practice which takes 30 minutes. Exercises include squats, balance training, and jump-landing exercises.</i_keyword>
      <i_keyword>Intervention group 2: This group will practice 6 weeks of plyometric-exercises without any visual feedback during the exercises, in a sports gym. Each week includes 3 sessions of practice which takes 30 minutes. Exercises include squats, balance training, and jump-landing exercises.</i_keyword>
      <i_keyword>Control group: This group will not receive any exercises from the assessor and continues their daily routine activities.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Lower extremity kinematics in 3 motion planes. Timepoint: before starting the interventions, and after 6 weeks of exercise interventions. Method of measurement: 8 Vicon motion capture cameras, a Kistler force plate.</prim_outcome>
      <prim_outcome>Lower extremity kinetics in 3 motion planes. Timepoint: before starting the interventions, and after 6 weeks of exercise interventions. Method of measurement: 8 Vicon motion capture cameras, a Kistler force plate.</prim_outcome>
      <prim_outcome>Dynamic balance. Timepoint: before starting the interventions, and after 6 weeks of exercise interventions. Method of measurement: Y-balance kit.</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 Tabataba'i University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-05-19</approval_date>
        <contact_name>University of Social Welfare and Rehabilitation Sciences</contact_name>
        <contact_address>kodakyar Ave., daneshjo Blvd.,Evin Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
