<?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>IRCT20210602051477N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-06-20</date_registration>
      <primary_sponsor>Kharazmi university</primary_sponsor>
      <public_title>The effect of neuromuscular and cognitive training on injury prevention</public_title>
      <acronym></acronym>
      <scientific_title>The effect of eight weeks of neuromuscular training with dual cognitive task on landing kinematic, proprioception and performance of futsal players with knee ligament dominance deficit</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-06-29</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/56804</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Other, Purpose: Prevention, Other design features: The present study has a control group (without intervention) and an experimental group (neuromuscular exercises with dual cognitive tasks), Randomization description: In order for the two study groups to have the same sample size, the law of random allocation will be used. The researcher first determines a total sample size (30 people) and then randomly assigns a set of them to the control group and the rest to the experimental group. The randomization unit is individual.
Randomly coded boxes will be used to hide random allocation. In this way, a number of boxes of the same size and shape will be randomly selected and inside the boxes, the intervention or tabs in which random allocation is recorded will be used, Blinding description: Subjects are randomly assigned to the intervention and control groups. And they do not know exactly what intervention they are receiving.
Data analysis and evaluations are performed by an analytical researcher (separate from the study researchers).</study_design>
      <phase>N/A</phase>
      <hc_freetext>Neuromuscular control deficit.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Neuromuscular training program (including bipedal squat, single-legged squat, jumping and jumping, standing single-legged on an unstable surface, etc.) and cognitive exercises (including computational tasks, reaction to colors, etc.) simultaneously to The duration is six weeks, 4 sessions per week and 45 minutes per session (10 minutes of warm-up, 30 minutes of core training and 5 minutes of cooling). Unstable surfaces such as balance balls are used to perform neuromuscular exercises. Intervention 2: Control group: The control group, like the experimental group, will first take the pre-test and then take the post-test after six weeks of normal daily 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:
Only part of the data, such as the original outcome information, can be shared

When:
The access period starts from 1400

To whom:
The data of the present study will be available to researchers, educators, athletes and therapists

Conditions:
The use of training protocols of the present study is allowed

Where to obtain:
to the address
majidhamoongard@gmail.com
  Visit

How to obtain:
Pre-test, intervention (six to eight weeks) and post-test

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Majid Hamoongard</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No 26, Qashq Tarash Alley, Azar St</address>
        <city>Qom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3714945131</zip>
        <telephone>+98 25 3775 6424</telephone>
        <email>majidhamoongard@gmail.com</email>
        <affiliation>Kharazmi university</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Majid Hamoongard</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No 26, Qashq Tarash Alley, Azar St</address>
        <city>Qom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3714945131</zip>
        <telephone>+98 25 3775 6424</telephone>
        <email>majidhamoongard@gmail.com</email>
        <affiliation>Kharazmi university</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>People with knee ligament dominance defects that will be assessed and identified by the tuck Jump Test
Men in the age range of 18-30 years
Participated in the sport of futsal or football in the last three years
Failure to participate in injury prevention programs in the past year and normal body mass index</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>30 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>History of neuromuscular disorders
History of anterior cruciate ligament injury or lower limb injury requiring surgery</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>Prevention</i_code>
      <i_code>Prevention</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Neuromuscular training program (including bipedal squat, single-legged squat, jumping and jumping, standing single-legged on an unstable surface, etc.) and cognitive exercises (including computational tasks, reaction to colors, etc.) simultaneously to The duration is six weeks, 4 sessions per week and 45 minutes per session (10 minutes of warm-up, 30 minutes of core training and 5 minutes of cooling). Unstable surfaces such as balance balls are used to perform neuromuscular exercises.</i_keyword>
      <i_keyword>Control group: The control group, like the experimental group, will first take the pre-test and then take the post-test after six weeks of normal daily activities.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The effect of eight weeks of neuromuscular training with dual cognitive task on landing kinematic, proprioception and performance of futsal players with knee ligament dominance deficit. Timepoint: Kinematic measurement, depth and function at the beginning of the study (before the intervention) and after eight weeks of the intervention. Method of measurement: Data collection form of subjects including (height, weight, body mass index, age, dominant foot, name, contact number, history of activity and history of lower extremity and brain injuries that affect cognitive and mental tasks Will be recorded.Camera: For 2D kinematic analysisQuinoa software: for two-dimensional kinematic analysisScales: To measure the weight of the subjects  Height meter: to measure the height of the subjects.</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>IR.SSRI.REC.1400.1071</sec_id>
        <issuing_authority>Institute of Physical Education and Sports Sciences</issuing_authority>
      </secondary_id>
    </secondary_ids>
    <source_support>
      <source_name>Kharazmi university</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-06-01</approval_date>
        <contact_name>Ethics Committee of the Institute of Physical Education and Sports Sciences</contact_name>
        <contact_address>No. 26, Qashq Tarash Alley, Azar St Qom Ghoum Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
