<?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>IRCT20230609058429N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2023-06-24</date_registration>
      <primary_sponsor>Razi University of Kermanshah</primary_sponsor>
      <public_title>The effect of eight weeks of Neuromuscular Dynamic Stability (DNS) exercise on motor performance indicators, kinematic gait, and lower limb injury indices</public_title>
      <acronym></acronym>
      <scientific_title>The effect of eight weeks of Neuromuscular Dynamic Stability (DNS) exercise on motor performance indicators, kinematic gait, and lower limb injury indices in physical education students with poor lumbar-pelvic control.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2023-07-10</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/70574</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: A researcher generates an allocation sequence with a block size of two using an online random number generator (Random.org). Patients will be randomly divided into one of two treatment groups in a ratio of 1:1 as follows: intervention group
  (n = 15) or control group (n = 15). The randomization is a number from 1 to 42 that is prepared in advance and placed in sealed opaque envelopes in a box. Participants will be told which intervention they were randomized to after eight weeks at the end of the study, Blinding description: Assessors will be blinded to group allocation. Investigators responsible for data analysis will use a coded dataset to ensure blinding. Patients will not be blinded to the exercise study, but will not know which treatment group they will be assigned to.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Lower limb injury.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: The intervention group will undergo neuromuscular stability training interventions for eight weeks. Intervention 2: Control group: This group does their routine activities for 8 weeks and does not participate in any training.</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 We have not reached the final conclusion yet</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>fatemeh ariyan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 136, 10th St, Ghaziabad</address>
        <city>Khorramabad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>No. 136, 10th St ,Gh</zip>
        <telephone>+98 83 3427 7605</telephone>
        <email>fatemehariyan67@gmail.com</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>fatemeh ariyan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 136, 10th St, Ghaziabad</address>
        <city>Khorramabad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6714414971</zip>
        <telephone>083-34277605-6</telephone>
        <email>fatemehariyan67@gmail.com</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Physical education students of Khorramabad schools
The age range is 15 to 17 years, second year of high school
The age range is 15 to 17 years, the second year of high school</inclusion_criteria>
      <agemin>15 years</agemin>
      <agemax>17 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Having a history of injury in the past 6 months in the trunk and lower limbs.
Having a history of surgery in the back area.
People with inflammatory disease of the spine
The presence of any significant abnormality in the alignment of the body.
People with a history of fracture in the spine, people with a history of tumor in the lower back.</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>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: The intervention group will undergo neuromuscular stability training interventions for eight weeks.</i_keyword>
      <i_keyword>Control group: This group does their routine activities for 8 weeks and does not participate in any training.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Dynamic balance. Timepoint: Data will be assessed at the two measurement time points from the participants:•	Before intervention;•	After intervention•. Method of measurement: Y balance test will be used to evaluate the dynamic balance of the subjects. The reliability of this test for assessing dynamic balance and correlation coefficient is reported as 0.86 to 0.96.</prim_outcome>
      <prim_outcome>Static balance. Timepoint: Data will be assessed at the two measurement time points from the participants:•	Before intervention;•	After intervention•. Method of measurement: To measure static balance, the test of standing on one leg (stork or stork) will be used, which will be included in the validity (0.79-0.64) and reliability (0.99-0.93) for this test.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Assessment of lumbar-pelvic control. Timepoint: The data will be measured at two time points: • before the intervention • after the intervention •. Method of measurement: In the sample of the current research, the pressure biofeedback device modeled and made in the United States of America, with a measurement range of 0-200 mm of mercury, and an accuracy of ±3 MHz pressure, in blue color, will be used to evaluate lumbar-pelvic control;.</sec_outcome>
      <sec_outcome>Landing mechanics. Timepoint: The data will be measured at two time points: • before the intervention • after the intervention •. Method of measurement: The LESS test is a clinical tool for dynamic movements that is used to identify inappropriate patterns during landing after jumping. It is performed in such a way that a person stands on a 30 cm box, then jumps forward from the box with both feet so that it lands at a distance of half its height, and then as soon as it lands, it jumps up to the maximum height and again. return to its original place. This test evaluates landing technique based on 9 images of landing and using 17 different questions on how to perform jump-landing skills using the system - two sagittal and frontal views.</sec_outcome>
      <sec_outcome>Motor function of the lower limb. Timepoint: The data will be measured at two time points: • before the intervention • after the intervention •. Method of measurement: In the present study, four tests (one-leg jump test, 3-step jump test, 6-meter jump test in time, cross jump test) will be used in order to evaluate the performance of the lower limb.</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>Razi University of Kermanshah</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2020-08-11</approval_date>
        <contact_name>Research Ethics Committee of Razi University of</contact_name>
        <contact_address>Razi University, University Street ,Taq Bostan, Kermanshah Kermanshah Kermanshah Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
