<?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>IRCT20240416061502N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-05-05</date_registration>
      <primary_sponsor>The University of Faisalabad</primary_sponsor>
      <public_title>Active Release Technique on Scapular Dyskinesia in Patients with Repetitive Shoulder Injuries</public_title>
      <acronym></acronym>
      <scientific_title>EFFECTS OF ACTIVE RELEASE TECHNIQUE ON SCAPULAR DYSKINESIA, PAIN, RANGE OF MOTION AND FUNCTIONAL LIMITATIONS IN PATIENTS WITH REPETITIVE SHOULDER INJURIES</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-02-06</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>24</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/76580</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Convenient Sampling Randomization/ an Individual unit was assigned to one of the groups/ The tools used were the Chit and Draw method, thoroughly mixed and randomly drawn, the resulting sequence was random. Allocation concealment of participants, Blinding description: Participants were blinded in my study until the cessation of treatment sessions.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Condition 1: Scapular Dyskinesia. Condition 2: Repetitive Shoulder Injuries.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Active Release Technique and Baseline Treatment (MWM Mobilization, Scapular Correction Exercises, Heating Modality). Intervention 2: Control group: Baseline Treatment (MWM Mobilization, Scapular Correction Exercises, Heating Modality).</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>Lyba Musaddiq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>25-W-8, Madina Town, Faisalabad</address>
        <city>Faisalabad</city>
        <country1>Pakistan</country1>
        <zip>38000</zip>
        <telephone>+92 322 6380789</telephone>
        <email>2022-ms-pt-028@tuf.edu.pk</email>
        <affiliation>The University of Faisalabad, Pakistan</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Lyba Musaddiq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>25-W-8, Madina Town, Faisalabad</address>
        <city>Faisalabad</city>
        <country1>Pakistan</country1>
        <zip>38000</zip>
        <telephone>+92 322 6380789</telephone>
        <email>2022-ms-pt-028@tuf.edu.pk</email>
        <affiliation>The University of Faisalabad, Pakistan</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
      <country2>Pakistan</country2>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Male and female aged 20 to 40 years
Patients who had scapular dyskinesia positive by Modified SAT and LSST
Patients who had pain score of 4 or more on the NPRS scale
Patients who had pain, impaired ROM, and functional limitation secondary to repetitive shoulder injuries
Patients who were willing to participate and filled the informed consent provided by the study protocol</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>40 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Individuals with significant comorbidities affecting treatment, such as severe cardiovascular disease or neuromuscular disorders, shoulder dislocation, active infection, arthritis, fracture, and dislocation/subluxation were excluded
Patients who had neurological injury such as Long Thoracic Nerve Injury
Patients who had acute shoulder surgeries and winged scapula were excluded due to variations in recovery.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M75.82</hc_code>
      <hc_code>M75.9</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Other shoulder lesions, left shoulder</hc_keyword>
      <hc_keyword>Shoulder lesion, unspecified</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: Active Release Technique and Baseline Treatment (MWM Mobilization, Scapular Correction Exercises, Heating Modality)</i_keyword>
      <i_keyword>Control group: Baseline Treatment (MWM Mobilization, Scapular Correction Exercises, Heating Modality)</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Scapular Dyskinesia. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: Ruler.</prim_outcome>
      <prim_outcome>Pain. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: NPRS Scale.</prim_outcome>
      <prim_outcome>Shoulder and Scapular Range of Motion. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: Goniometer and Digital Inclinometer.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Functional Limitation. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: SPADI Questionnaire.</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>Madinah Teaching Hospital</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-02-17</approval_date>
        <contact_name>Ethical Committee of The University of Faisalabad</contact_name>
        <contact_address>West Canal Road, Faisalabad-37610 Faisalabad Punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
