<?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>IRCT20190904044693N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-08-06</date_registration>
      <primary_sponsor>Muhammad Institute of Medical and Allied Sciences, Multan</primary_sponsor>
      <public_title>Effectiveness of muscle energy technique and posterior shoulder mobilization with movement in patients with subacromial pain syndrome</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of muscle energy technique and posterior shoulder mobilization with movement in patients with subacromial pain syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-04-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>56</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/65084</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The 56 patients diagnosed with shoulder pain syndrome referred by the orthopedic surgeons will be screened for eligibility.  The 40 patients meeting the eligibility criteria will be randomized into two equal groups. The patients will be randomly allocated (20/group) through online computer generated random number table. Every subject will be assigned a random number from the table on recruitment.
Online table will be generated by using this site: https://www.random.org/sequences/?mode=advanced
Smallest value: 1
Largest value: 40
The format in Column: 2
The sequence of numbers 20 will be randomly allocated in column 1, and 20 will be allocated in column 2, Blinding description: The outcome assessor will be the consultant physical therapist of setting department of physical therapy, Bakhtawar Amin Trust and Teaching Hospital, Multan. Outcomes will be measured at baseline before starting treatment and end of treatment after 6 week. Outcome assessor will be unaware about treatment given to any particular subject. 
Data will be analysed by statistician without knowing the treatment regime received both groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Subacromial Pain Syndrome.</hc_freetext>
      <i_freetext>Intervention 1: Muscle Energy Technique: Post isometric muscle relaxation technique of METs will be used to improve outcome measures in patients with subacromial pain syndrome.  Patient will be in supine lying position and will be asked for 7-10 seconds sustained contraction of muscle against the therapist hold by using 20-30% force of body. Then therapist will move the limb passively in shoulder range until new barrier will be found and same procedure will be repeated to eliminate the barrier. Patients will be treated on alternative days  for 6 weeks. Intervention 2: Posterior shoulder mobilization with movement: One hand of the physical therapist stabilizes the patients shoulder girdle. While other hand will perform a posterior-lateral glide of the humeral head. Patients will be asked to raise the affected arm to find the new point of pain onset and therapist will sustain the gliding force.  The therapist will maintain the gliding at right angle of movement throughout the entire active range performed by patients. The entire procedure of mobilization will be pain free and patients will be instructed to report any pain and discomfort.</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:
Effectiveness of muscle energy technique and posterior shoulder mobilization with movement in patients with subacromial pain syndrome

When:
The data will be available after publication of this research study

To whom:
Data document will be available to corresponding author

Conditions:
Data could be used only for research purpose

Where to obtain:
Data will be obtainable on request to corresponding author

How to obtain:
Through email to shahidishaq53@gmail.com

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Shahid Ishaq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Southren ByPass, Multan</address>
        <city>Multan</city>
        <country1>Pakistan</country1>
        <zip>60000</zip>
        <telephone>+92 305 2032722</telephone>
        <email>shahidishaq53@gmail.com</email>
        <affiliation>Bakhtawar Amin College of Rehabilitation Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Shahid Ishaq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Southern bypass, Multan</address>
        <city>Multan</city>
        <country1>Pakistan</country1>
        <zip>60000</zip>
        <telephone>+92 305 2032722</telephone>
        <email>shahidishaq53@gmail.com</email>
        <affiliation>Bkhtawar Amin College of Rehabilitation Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Patient diagnosed with subacromial  pain syndrome by orthopedic surgeon
History of unilateral subacromial pain for minimum of 3 months
Painful arc in shoulder abduction  range 70° -120°
Pain aggravates upon resisted muscle testing in abduction and lateral rotation
At least three positive physical tests from followings Neer impingement test, Hawkins kneddy test, Drop arm test, relocation test
Positive shoulder abduction stress test</inclusion_criteria>
      <agemin>30 years</agemin>
      <agemax>60 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Patients potentially not willing to participate in study
Patients with recent history of fall, upper limb fracture and shoulder surgery
Degenerative joint disease of affected shoulder
Cervical radiculopathy
Frozen shoulder
shoulder bursitis
Associated systemic disease</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Subacromial Pain Disease</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Muscle Energy Technique: Post isometric muscle relaxation technique of METs will be used to improve outcome measures in patients with subacromial pain syndrome.  Patient will be in supine lying position and will be asked for 7-10 seconds sustained contraction of muscle against the therapist hold by using 20-30% force of body. Then therapist will move the limb passively in shoulder range until new barrier will be found and same procedure will be repeated to eliminate the barrier. Patients will be treated on alternative days  for 6 weeks.</i_keyword>
      <i_keyword>Posterior shoulder mobilization with movement: One hand of the physical therapist stabilizes the patients shoulder girdle. While other hand will perform a posterior-lateral glide of the humeral head. Patients will be asked to raise the affected arm to find the new point of pain onset and therapist will sustain the gliding force.  The therapist will maintain the gliding at right angle of movement throughout the entire active range performed by patients. The entire procedure of mobilization will be pain free and patients will be instructed to report any pain and discomfort.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Shoulder pain severity. Timepoint: Before and after 6 week successful completion of follow ups. Method of measurement: Numeric Pain Rating Scale (NPRS).</prim_outcome>
      <prim_outcome>Shoulder physical disability. Timepoint: Before and after 6 week successful completion of follow ups. Method of measurement: Shoulder pain and Disability Index (SPADI).</prim_outcome>
      <prim_outcome>Shoulder range of motion (ROM). Timepoint: Before and after 6 week successful completion of follow ups. Method of measurement: Universal goniometer.</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>Nill</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-04-10</approval_date>
        <contact_name>Research ethics committee of Muhammad Institute of Medical and Allied Sciences</contact_name>
        <contact_address>HBL Street, Near Sabzazar Metro Station, Bosan Raod Multan Multan Punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
