<?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>IRCT20230612058457N6</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-06-04</date_registration>
      <primary_sponsor>University of Guilan</primary_sponsor>
      <public_title>Comparison of the Effects of Static Stretching and Dynamic Warm-up on Shoulder Performance in Athletes with Shoulder Impingement Syndrome</public_title>
      <acronym></acronym>
      <scientific_title>Acute Effects of Static Stretching and Dynamic Warm-up on Shoulder Performance in Male Athletes with Shoulder Impingement Syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-06-09</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>50</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/83943</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Other design features: This study will be a randomized controlledl trial, Randomization description: In this study, to allocate participants into three intervention groups (static stretching, dynamic warm-up, and combined), simple randomization with block randomization will be used. The unit of randomization will be the individual, and the allocation sequence to groups will be generated using the RandBox.top website with the method of balanced blocks. If controlling for confounding variables such as type of exercise or symptom severity is necessary, stratified randomization will be applied. To conceal the allocation (Allocation Concealment), sealed envelopes containing group codes will be used, which will be opened by an independent person after enrollment and pre-testing. These methods will ensure that the distribution of participants across groups is balanced and unpredictable, Blinding description: In the present study, the researcher recording the research variables is unaware of the participants' allocation to the exercise protocols.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Shoulder impingement syndrome.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Athletes with shoulder impingement syndrome participating in a static stretching protocol. The protocol includes six targeted active soft-tissue stretches for the shoulder, with each stretch performed in 3 sets of 30 seconds, and 15 seconds of rest between sets. The total duration of the protocol is approximately 10 minutes. Intervention 2: Intervention group: Athletes with shoulder impingement syndrome participating in a dynamic warm-up protocol. The protocol includes six dynamic exercises using a yellow resistance band, with each exercise performed for 10 repetitions at a speed of 2 seconds per repetition. Intervention 3: Intervention group: Athletes with shoulder impingement syndrome who participate in the combined protocol. This protocol includes three exercises from the static stretching protocol and three exercises from the dynamic warm-up protocol, performed with the same timing and structure as the other groups. The exercises include: shoulder extension, deltoid stretch, scapular punch, pectoralis major stretch, throwing acceleration, and triceps stretch. Intervention 4: Control group: Healthy athletes without symptoms of shoulder impingement syndrome who participate in all three intervention protocols (static stretching, dynamic warm-up, and a combination of static stretching and dynamic warm-up). This group is included for comparison of responses with the intervention groups (athletes with the condition). The order of protocol implementation is randomized, with a 72-hour interval between sessions.</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:
En All data will be shared after anonymizing individuals, ensuring their non-identifiability.

When:
The data access period will start immeduately after the results are printed.

To whom:
The data will be accessible to researchers and organizations related to sports disciplines where the shoulder joint is the main involved joint.

Conditions:
In order to assist scientific research and promote the implementation of executive goals with a focus on reducing musculoskeletal injuries and enhancing the performance of athletes.

Where to obtain:
Mohammad Alimoradi/malimoradi@sport.uk.ac.ir

How to obtain:
Requests for access to data will be answered within a week

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mohammad Alimoradi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Unit 6, Yekta residential complex, Fathalishahi 12 St, Kerman, Iran</address>
        <city>Kerman</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7614816961</zip>
        <telephone>+98 34 2250 1685</telephone>
        <email>malimoradi@sport.uk.ac.ir</email>
        <affiliation>Shahid Bahonar University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mohammad Alimoradi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Unit 6, Yekta residential complex, Fathalishahi 12 St, Kerman, Iran</address>
        <city>Kerman</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7614816961</zip>
        <telephone>+98 34 2250 1685</telephone>
        <email>malimoradi@sport.uk.ac.ir</email>
        <affiliation>Shahid Bahonar University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Sex: Male
Age range: 20 to 30 years
Pain in the arc of motion (between 60 and 120 degrees) during shoulder flexion or extension.
Positive Neer or Hawkins-Kennedy test.
Pain during resisted external rotation, shoulder abduction, or positive Jobe test.
Positive Apprehension-Relocation test (without posterior pain).</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>30 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>History of shoulder surgery or dislocation.
Currently receiving physiotherapy or medication treatment for the shoulder.
Performed heavy exercises within 48 hours before the test.
Lack of cooperation or withdrawal from continuing the study.
Presence of other neuromuscular or musculoskeletal diseases affecting the shoulder (such as rheumatoid arthritis, rotator cuff tear).</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M75.4</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Impingement syndrome of shoulder</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Athletes with shoulder impingement syndrome participating in a static stretching protocol. The protocol includes six targeted active soft-tissue stretches for the shoulder, with each stretch performed in 3 sets of 30 seconds, and 15 seconds of rest between sets. The total duration of the protocol is approximately 10 minutes.</i_keyword>
      <i_keyword>Intervention group: Athletes with shoulder impingement syndrome participating in a dynamic warm-up protocol. The protocol includes six dynamic exercises using a yellow resistance band, with each exercise performed for 10 repetitions at a speed of 2 seconds per repetition.</i_keyword>
      <i_keyword>Intervention group: Athletes with shoulder impingement syndrome who participate in the combined protocol. This protocol includes three exercises from the static stretching protocol and three exercises from the dynamic warm-up protocol, performed with the same timing and structure as the other groups. The exercises include: shoulder extension, deltoid stretch, scapular punch, pectoralis major stretch, throwing acceleration, and triceps stretch.</i_keyword>
      <i_keyword>Control group: Healthy athletes without symptoms of shoulder impingement syndrome who participate in all three intervention protocols (static stretching, dynamic warm-up, and a combination of static stretching and dynamic warm-up). This group is included for comparison of responses with the intervention groups (athletes with the condition). The order of protocol implementation is randomized, with a 72-hour interval between sessions.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>In the present study, the range of motion of internal and external rotation of the shoulder joint will be examined. Timepoint: At the beginning of the study (before the intervention), 5 minutes after the intervention, and one hour after the intervention. Method of measurement: It is measured using a goniometer.</prim_outcome>
      <prim_outcome>The present study investigates the stability of the shoulder joint. Timepoint: At the beginning of the study (before the intervention), 5 minutes after the intervention, and one hour after the intervention. Method of measurement: It is assessed using the Y test.</prim_outcome>
      <prim_outcome>The present study investigates the proprioception of the shoulder joint. Timepoint: At the beginning of the study (before the intervention), 5 minutes after the intervention, and one hour after the intervention. Method of measurement: It is evaluated using target angle reconstruction and photography.</prim_outcome>
      <prim_outcome>The present study examines isokinetic and isometric strength of the shoulder joint during internal and external rotation, assessed through concentric and eccentric contractions. Timepoint: At the beginning of the study (before the intervention), 5 minutes after the intervention, and one hour after the intervention. Method of measurement: It is evaluated using an isokinetic dynamometer.</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>University of Guilan</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-05-19</approval_date>
        <contact_name>Research Ethics Committees of University of Guilan</contact_name>
        <contact_address>5th Kilometer of Persian Gulf Highway, Rasht, Guilan Province, Iran Rasht Guilan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
