<?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>IRCT20260910070994N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-10-01</date_registration>
      <primary_sponsor>The University of Guilan</primary_sponsor>
      <public_title>The Effect of Two Injury-Prevention Warm-Up Programs on Knee Injury Risk Factors in Basketball Players</public_title>
      <acronym></acronym>
      <scientific_title>The effect of FIFA 11+ and SHRed warm-up programs on knee injury risk factors in female basketball players</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-12-01</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/93236</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention, Randomization description: Eligible participants were randomly allocated to two groups (15 participants in each group) using the lottery method with sealed envelopes labeled A and B. One group received the FIFA 11+ program and the other received the SHRed program.</study_design>
      <phase>N/A</phase>
      <hc_freetext>1. Assessment of ankle dorsiflexion range of motion 2. Assessment of ankle plantarflexion range of motion 3. Assessment of knee proprioception at 30 and 60 degrees 4. Assessment of Landing Error Screening Score.</hc_freetext>
      <i_freetext>Intervention 1: The FIFA 11+ protocol is a standardized warm-up program that consists of three main parts: the first part is active running and warm-up exercises, the second part is strength, plyometric, and balance exercises, and the third part is acceleration and change of direction. This protocol was usually performed for 6 weeks, three sessions per week, each session lasting 20 minutes. The warm-up program began with easy-level exercises in the first sessions, and the level of difficulty of the exercises increased over time. Studies have shown that performing FIFA 11+ can reduce the risk factors for knee injuries, including neuromuscular control and muscle balance. The warm-up process in FIFA 11+ was implemented as follows: first, the athlete performed light running exercises and active movements; then, with strength, balance, and jumping exercises, the muscles and joints were prepared for explosive movements and rapid changes of direction; and finally, the warm-up ended with explosive running and agility exercises. Also, the level of exercises (from Level 1-3), number of sets, and repetitions were adjusted each week according to the participants' overall progress. Intervention 2: The SHRed is a standardized 10–15 min protocol that includes three main parts and 13 exercises in total. It includes aerobic and mobility exercises (e.g., running and changing direction), strength exercises (e.g., core stability and Nordic hamstring exercises), agility exercises (e.g., changing direction and cutting), and balance exercises (e.g., standing on one leg). In the present study, the protocol was conducted by the participants for 6 weeks, with three sessions per week, each lasting 10 - 15 min, under the supervision of the researcher and a physiotherapist with 3 years of clinical experience before each training session. Also, according to the original protocol instructions, the exercise level in each part ranged from level 1 to level 2, depending on participants’ progress in each part.</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 There is no further information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ali Shamsimajelan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>University of Guilan Complex, Km 5 Tehran Road, Persian Gulf Highway, Rasht, Iran</address>
        <city>Rasht</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4199613776</zip>
        <telephone>+98 13 3369 0274</telephone>
        <email>alishamsim@yahoo.com</email>
        <affiliation>The University of Guilan</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Ali Shamsimajelan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>University of Guilan Complex, Km 5 Tehran Road, Persian Gulf Highway, Rasht, Iran</address>
        <city>Rasht</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4199613776</zip>
        <telephone>+98 13 3369 0274</telephone>
        <email>alishamsim@yahoo.com</email>
        <affiliation>The University of Guilan</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Female basketball players
Aged 18 to 25
At least 3 years of experience in basketball
Experience participating in provincial-level competitions and team training sessions
Regular training routine (at least three sessions per week)
No history of lower-limb injury within the past 6 months</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>25 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Three non-consecutive absences or two consecutive absences during the warm-up program period
Previous injury or surgery, particularly in the lower extremities
History of chronic diseases or use of neurological medications
Withdrawal or unwillingness to cooperate
Failure to adhere to the warm-up program guidelines</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>The FIFA 11+ protocol is a standardized warm-up program that consists of three main parts: the first part is active running and warm-up exercises, the second part is strength, plyometric, and balance exercises, and the third part is acceleration and change of direction. This protocol was usually performed for 6 weeks, three sessions per week, each session lasting 20 minutes. The warm-up program began with easy-level exercises in the first sessions, and the level of difficulty of the exercises increased over time. Studies have shown that performing FIFA 11+ can reduce the risk factors for knee injuries, including neuromuscular control and muscle balance. The warm-up process in FIFA 11+ was implemented as follows: first, the athlete performed light running exercises and active movements; then, with strength, balance, and jumping exercises, the muscles and joints were prepared for explosive movements and rapid changes of direction; and finally, the warm-up ended with explosive running and agility exercises. Also, the level of exercises (from Level 1-3), number of sets, and repetitions were adjusted each week according to the participants' overall progress.</i_keyword>
      <i_keyword>The SHRed is a standardized 10–15 min protocol that includes three main parts and 13 exercises in total. It includes aerobic and mobility exercises (e.g., running and changing direction), strength exercises (e.g., core stability and Nordic hamstring exercises), agility exercises (e.g., changing direction and cutting), and balance exercises (e.g., standing on one leg). In the present study, the protocol was conducted by the participants for 6 weeks, with three sessions per week, each lasting 10 - 15 min, under the supervision of the researcher and a physiotherapist with 3 years of clinical experience before each training session. Also, according to the original protocol instructions, the exercise level in each part ranged from level 1 to level 2, depending on participants’ progress in each part.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Measurement of ankle dorsiflexion range of motion. Timepoint: Before the intervention and after the intervention for one and a half months. Method of measurement: Using a universal goniometer.</prim_outcome>
      <prim_outcome>Measurement of ankle plantarflexion range of motion. Timepoint: Before the intervention and after the intervention for one and a half months. Method of measurement: Using a universal goniometer.</prim_outcome>
      <prim_outcome>Measurement of knee proprioceptive recovery at a 30-degree angle. Timepoint: Before the intervention and after the intervention for one and a half months. Method of measurement: Using a universal goniometer.</prim_outcome>
      <prim_outcome>Measurement of knee proprioceptive recovery at a 60-degree angle. Timepoint: Before the intervention and after the intervention for one and a half months. Method of measurement: Using a universal goniometer.</prim_outcome>
      <prim_outcome>Evaluation of the Landing Error Scoring System (LESS) score. Timepoint: Before the intervention and after the intervention for one and a half months. Method of measurement: Using a specific scoring table based on a reliable reference.</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>The University of Guilan</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-07-14</approval_date>
        <contact_name>University of Guilan Ethics Committee</contact_name>
        <contact_address>University of Guilan Complex, Km 5 Tehran Road, Persian Gulf Highway, Rasht, Iran Rasht Guilan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
