<?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>IRCT20240907062968N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-11-18</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>The Effect Of Adding Selevtive Neuromuscular Exercise to Conventional Basketball Exercises on Some of the Risk Factors</public_title>
      <acronym></acronym>
      <scientific_title>The Effect Of Adding Selevtive Neuromuscular Exercise to Conventional Basketball Exercises on Some of the Risk Factors in Adolescent Semi-Professional Basketball Players.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2023-11-03</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/78911</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention, Randomization description: The randomization method will be web-based. Subjects who meet the inclusion criteria are randomly divided into the control group and injury prevention exercises using the randomization method of the website (Social Psychology Network, Connecticut, USA) www.randomizer.org. Randomization will be simple. Concealment of random allocation using a computer-generated block randomization table, where the number 1 will be defined for the training group, and the number 2 will be defined for the control group. Then the random number sequence will be placed in opaque and sealed envelopes. Also, according to the assignment of the group, the intervention by the researcher will continue. Finally, it will evaluate the results before the interventions and eight weeks after the interventions, Blinding description: After reading the consent form, the participants were informed about the study groups in a 30-minute meeting, and without having the right to choose the group, they participated in this study with their consent, so that the names of the patients were entered by someone who was not aware of the identity and physical characteristics of the individuals. Using the site /http://randomizer.org, it is randomly divided into two equal groups and each part is placed separately in sealed envelopes. Then, according to their assigned group, relevant training and exercises are provided to each person. The outcome analyzer and evaluator also examines and compares the changes made before and after eight weeks without knowing the hypotheses, study methods and patient characteristics.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Risk factors of lower limb and trunk injury.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Neuromuscular exercises were performed in the warm-up for 20 minutes before regular basketball exercises, and then they performed basketball exercises for 90 minutes, 3 sessions per week for 8 weeks. Intervention 2: Control group: They only did common basketball exercises for 90 minutes, 3 sessions a week.</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:
The data related to the subjects of the control and intervention groups in the pre-test and post-test are shared in an unidentifiable way.

When:
Six months after the publication of articles

To whom:
All researchers

Conditions:
There is no obstacle to using data for citation, by mentioning the source.

Where to obtain:
Vahid.mazloum@yahoo.com

How to obtain:
The request will be made by email and the answer will be sent within 15 days.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Vahid Mazloum</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Rajaie shahr, Moazen bolvd, Islamic Azad university of Karaj branch</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3149968111</zip>
        <telephone>+98 26 3425 9571</telephone>
        <email>Vahid.mazloom@kiau.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Vahid Mazloum</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Rajie shahr, MOazan Bolvd, Islamic Azad university of Karaj Branch</address>
        <city>کرج</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3149968111</zip>
        <telephone>009826364529571</telephone>
        <email>Vahid.mazloom@kiau.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>The participants should have the ability to participate in the national league teams in terms of the quality level of the game
Having at least three years of playing experience in national championships or national leagues
Having general health approval by a doctor</inclusion_criteria>
      <agemin>13 years</agemin>
      <agemax>18 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>The presence of abnormalities in the trunk and lower limbs
Players who have not had any injury, pain or surgery in the lower limbs and trunk in the last six months</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 exercises were performed in the warm-up for 20 minutes before regular basketball exercises, and then they performed basketball exercises for 90 minutes, 3 sessions per week for 8 weeks.</i_keyword>
      <i_keyword>Control group: They only did common basketball exercises for 90 minutes, 3 sessions a week.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The Landing Error Scoring System. Timepoint: Before and after intervention. Method of measurement: The landing error scoring system.</prim_outcome>
      <prim_outcome>Knee-valgus and flexion moment. Timepoint: Before and after intervention. Method of measurement: Two cameras will be used to evaluate the dynamic valgus and flexion of the knee.</prim_outcome>
      <prim_outcome>Trunk endurance of extensor muscles. Timepoint: Before and after intervention. Method of measurement: Biering–Sorensen.</prim_outcome>
      <prim_outcome>Proprioception test. Timepoint: Before and after intervention. Method of measurement: 30 degree angle.</prim_outcome>
      <prim_outcome>Dynamic Balance. Timepoint: Before and after intervention. Method of measurement: It was measured in 3 directions with the star test.</prim_outcome>
      <prim_outcome>Sarjent jump. Timepoint: Before and after intervention. Method of measurement: tape measure.</prim_outcome>
      <prim_outcome>Illinoise test. Timepoint: Before and after intervention. Method of measurement: Illinois standardized test.</prim_outcome>
      <prim_outcome>T-test. Timepoint: Before and after intervention. Method of measurement: T-test standardized test.</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</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-08-26</approval_date>
        <contact_name>Ethics Committee of Islamic Azad University Karaj branch</contact_name>
        <contact_address>Rajaie shahr, Moazzen Bolvd, Islamic azad university Karaj branch karaj Alborz Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
