<?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>IRCT20250827067022N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-09-22</date_registration>
      <primary_sponsor>Kharazmi University</primary_sponsor>
      <public_title>Effect of scapula - focused and kinetic chain exercises in athletes with scapula dyskinesia</public_title>
      <acronym></acronym>
      <scientific_title>Comparison the Effect of Scapula-Focused Exercises and Kinetic Chain Rehabilitation on Strength, proprioception, pain and disability on Athletes with Scapula Dyskinesia</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-10-03</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/86167</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Following the baseline examination, by using the method on the website http://randomizer.org participants are randomly assigned into the two experimental groups (neuromuscular training with an attentional focus), (therapeutic exercise), and control group. Simple randomization is used. Concealed allocation is performed using a computer generated block randomized table of numbers ( 1 and 2 for experimental groups and 3 for control group) created before the start of data collection by researcher who is not involved in the recruitment or treatment of patients. Then, the random numerical sequence is placed in sealed opaque envelope and processed with treatment according to the group assignment. A blinded outcome assessor who does not know the hypothesis and study methods, measures outcome at baseline and 8 weeks post-intervention, Blinding description: In this study, blinding will be carried out in a single-blind manner. This means that only the participants and outcome assessor will be unaware of the type of intervention and the group to which they have been allocated (experimental or control), while the main researchers will be aware of the allocation. To minimize bias, the allocation of participants to groups will be performed using a block randomization method by an individual independent from the data collection team. Participants will be informed that they are taking part in a comparative study, but details about the exact type of intervention and the differences between groups will not be disclosed. All interventions will be delivered under similar timing and environmental conditions so that no obvious differences are detectable by the participants. Additionally, participants will be asked to refrain from inquiring about the type of intervention or comparisons with the other group. Data collection will be carried out by a trained assessor who, as much as possible, will remain minimally informed about the final objectives and main hypotheses of the study, in order to reduce observer bias in outcome measurement. In case of circumstances where blinding may be compromised (such as direct questioning by a participant or specific side effects), such events will be documented and considered in the final analysis.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Scapula dyskinesia.</hc_freetext>
      <i_freetext>Intervention 1: First Intervention group: The scapula-focused exercise protocol was implemented over 8 weeks with three 60-minute sessions per week. Each session included a 10-minute warm-up, the main exercise phase, and a 10-minute cool-down. The main phase consisted of 8 selected exercises designed to strengthen and stabilize key scapular muscles, including the serratus anterior, middle and lower trapezius, and the rotator cuff. Each exercise was performed in 3 sets of 10 repetitions, and progression was applied by gradually increasing the number of sets and repetitions to enhance shoulder strength, stability, and scapulohumeral rhythm in a structured manner. Intervention 2: Second Intervention group: The kinetic chain rehabilitation protocol was carried out over 8 weeks, with three 60-minute sessions per week. Each session consisted of a 10-minute dynamic warm-up, the main exercise phase, and a 10-minute cool-down. The main phase included 11 selected exercises designed to integrate the upper limbs, trunk, and lower limbs through kinetic chain patterns. These exercises involved movements such as lunges with overhead press, diagonal chop and lift, push-up plus, single-leg squat with reach, and dynamic throwing or pulling tasks, aiming to simulate force transmission from the lower limbs to the shoulder girdle. Each exercise was initially performed in 3 sets of 10 repetitions, with progression achieved by gradually increasing to 4 sets of 12 repetitions and then 5 sets of 10 repetitions. This structured progression was intended to enhance neuromuscular coordination, improve force transfer, and optimize functional performance in both daily and sport-related activities. Intervention 3: Control group: The control group will not receive any intervention during the 8 week training protocol comprises kinetic chain and scapula focused exercises and they will continue their daily routine basis.</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 No more available data</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Seyed Sadr-o-din Shoja-o-din</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Center for Human Movement Sciences Kharazmi University Mirdamad, South Razan Street, Hesari Street, Keshvari Sport Complex</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1571914911</zip>
        <telephone>+98 21 2222 1008</telephone>
        <email>sa_shojaedin@yahoo.com</email>
        <affiliation>Kharazmi University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Seyed Sadr-o-din Shoja-o-din</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Center for Human Movement Sciences Kharazmi University Mirdamad, South Razan Street, Hesari Street, Keshvari Sport Complex</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1571914911</zip>
        <telephone>+98 21 2222 1008</telephone>
        <email>sa_shojaedin@yahoo.com</email>
        <affiliation>Kharazmi University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Aged between 18 and 30
Being male with at least 3 years experience in overhead sports
A positive Kibler lateral scapula side test performed by a physiotherapist
Pain intensity of 3 to 7 on the Visual Analog Scale</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>30 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>Lack of willingness or dissatisfaction of the individual to participate in or continue the test
Abnormal body mass index
History of trauma, fracture or shoulder joint dislocation
Limited shoulder range of motion
History of upper limb surgery in the past 2 years
Presence of structural abnormalities in the shoulder or thoracic, such as kyphosis or scoliosis
Presence of neurological or musculoskeletal diseases that cause movement limitations</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M25.819</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Other specified joint disorders, unspecified shoulder</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>First Intervention group: The scapula-focused exercise protocol was implemented over 8 weeks with three 60-minute sessions per week. Each session included a 10-minute warm-up, the main exercise phase, and a 10-minute cool-down. The main phase consisted of 8 selected exercises designed to strengthen and stabilize key scapular muscles, including the serratus anterior, middle and lower trapezius, and the rotator cuff. Each exercise was performed in 3 sets of 10 repetitions, and progression was applied by gradually increasing the number of sets and repetitions to enhance shoulder strength, stability, and scapulohumeral rhythm in a structured manner.</i_keyword>
      <i_keyword>Second Intervention group: The kinetic chain rehabilitation protocol was carried out over 8 weeks, with three 60-minute sessions per week. Each session consisted of a 10-minute dynamic warm-up, the main exercise phase, and a 10-minute cool-down. The main phase included 11 selected exercises designed to integrate the upper limbs, trunk, and lower limbs through kinetic chain patterns. These exercises involved movements such as lunges with overhead press, diagonal chop and lift, push-up plus, single-leg squat with reach, and dynamic throwing or pulling tasks, aiming to simulate force transmission from the lower limbs to the shoulder girdle. Each exercise was initially performed in 3 sets of 10 repetitions, with progression achieved by gradually increasing to 4 sets of 12 repetitions and then 5 sets of 10 repetitions. This structured progression was intended to enhance neuromuscular coordination, improve force transfer, and optimize functional performance in both daily and sport-related activities.</i_keyword>
      <i_keyword>Control group: The control group will not receive any intervention during the 8 week training protocol comprises kinetic chain and scapula focused exercises and they will continue their daily routine basis.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain. Timepoint: Pre-test( before the start of the study) and post-test(at the end of the study). Method of measurement: The pain variable was measured by a visual pain intensity scale.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Disability. Timepoint: Pre-test (before the start of the study) and post-test (at the end of the study). Method of measurement: The DASH questionnaire was used to assess functional impairment in daily activities.</sec_outcome>
      <sec_outcome>Muscle strength. Timepoint: Pre-test (before the start of the study) and post-test (at the end of the study). Method of measurement: Shoulder muscle strength during internal and external rotation was assessed in a concentric–concentric mode using an isokinetic dynamometer under standardized laboratory conditions.</sec_outcome>
      <sec_outcome>Joint position sense. Timepoint: Pre-test (before the start of the study) and post-test (at the end of the study). Method of measurement: Active proprioception of the shoulder during internal and external rotation was measured using an isokinetic dynamometer.</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>No governmental fund has been received for this study, and it is conducted by researchers.</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-06-25</approval_date>
        <contact_name>Ethics committee of Kharazmi University</contact_name>
        <contact_address>Faculty of physical education; south razan; mirdamad;tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
