<?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>IRCT20220712055441N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-07-15</date_registration>
      <primary_sponsor>Muhammad Institute of Medical and Allied Sciences, Multan</primary_sponsor>
      <public_title>Upper Thoracic and Postrior Shoulder sustained Stretch Glide</public_title>
      <acronym>UTSSM</acronym>
      <scientific_title>Effectiveness of Upper Thoracic Sustained Stretch Mobilization and Posterior Shoulder Strech Glide for Subacromial Impingement Syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-01-08</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>46</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/64744</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: thoracic  kyphosis will be measured by using an inclinometer shoulder ROM will be measured by a universal goniometer, pain intensity will be measure by NPRS, shoulder disability will be measured by shoulder pain and disability index, Randomization description: The patietns diagnosed with subacromial impingement syndrome (SIS) (n=46)referred by orthopedic surgeon will be secrened for eligibility. The patients (n=40) meet the eligibility criteria will be randomly allocated in two equal groups (n=20) in each group through online computer generated random number table. Every participant will be assigned a random number after writtten informed consent, Blinding description: In this double-blinded study, outcomes will be measured at baseline and after completing 4 weeks successful followup by senior physical therapist with out knowing treatment regimn given to that particular patient.
Data will be analyzed by statistician without knowing  the intervention given to any particular group.</study_design>
      <phase>2-3</phase>
      <hc_freetext>subacromial impingement syndrome.</hc_freetext>
      <i_freetext>Intervention 1: Group A  will recieve upper thoracic (T1-T4) centrally postrio-anterior sustained stretch mobilization. The patient was in prone and a small pillow was placed under the chest. Therapist applied central posterior-anterior (CPA) mobilization force with straight arm by using body as mobilizing force. The mobilization was given beyond transition zone for grade 3 stretching of joint capsule and soft tissue. Each stretch was sustained for 30-40 second and repeated in cyclic manner for 3 time per session. This mobilization treatment was applied parallel to routine physical therapy. All patients will be treated paralelly 3 time a week for 4 weeks. Intervention 2: Group B will posterior shoulder sustained stretch glide. The patient will be in supine laying near the edge of treatment table. The therapist will distract the joint in open pack position and apply grade 3 stretch glide to posterior shoulder capsule. Each stretch will be sustained for 30-40 second. The treatment will be cyclically repeated for 3 time per session. All patients will be treated paralelly 3 time a week for 4 weeks.</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:
Title: Effectiveness of Upper thoracic sustained stretch mobilization and Posterior shoulder stretch glide for Subacromial Impingement Syndrome
Purpose: to evaluate the comparative effectiveness of upper thoracic sustained stretch mobilization and posterior shoulder stretch glide for management of SIS symptoms severity such as shoulder pain, disability, range of motion and thoracic kyphosis angle.

When:
this is expected that this study or data will be available at the end of the year. no exact date can be expected

To whom:
Shahid Ishaq

Conditions:
For research purposes

Where to obtain:
https://www.researchgate.net/
https://scholar.google.com/

How to obtain:
open access

Comments:
This randomized clinical trial will explore the new dimentions of SIS treatment.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Shahid Ishaq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>HBL street, near sabza zar metro station, bosan road, Multan</address>
        <city>Multan</city>
        <country1>Pakistan</country1>
        <zip>60700</zip>
        <telephone>+92 305 2032722</telephone>
        <email>shahidishaq53@gmail.com</email>
        <affiliation>Muhammad Institute of Medical and Allied Science</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Shahid Ishaq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>HBL, Street, Near Sabzazar Metro Station, Bosan Road, Multan</address>
        <city>Multan</city>
        <country1>Pakistan</country1>
        <zip>60700</zip>
        <telephone>+92 305 2032722</telephone>
        <email>shahidishaq53@gmail.com</email>
        <affiliation>Muhammad Institute of Medical and Allied Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Both male and female, of age 25-45 years
Patients with thoracic kyphosis &gt;40o
Patients with at least three positive physical tests from followings Neer impingement test, Hawkins kneddy test, Drop arm test, relocation test and apprehension test will be included.
Patients often have painful arc between 70° and 120° pain on forced movement above the head</inclusion_criteria>
      <agemin>25 years</agemin>
      <agemax>45 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>History of rotator cuff tear, shoulder and cervicothoracic surgery
Patients of scapulothoracic dysfunction, sensory/ motor deficit and adhesive capsulitis
Osteoporosis
Surgery
Fractures
Dislocations
Presence of thoracic scoliosis on Adam’s forward bend test</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>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Group A  will recieve upper thoracic (T1-T4) centrally postrio-anterior sustained stretch mobilization. The patient was in prone and a small pillow was placed under the chest. Therapist applied central posterior-anterior (CPA) mobilization force with straight arm by using body as mobilizing force. The mobilization was given beyond transition zone for grade 3 stretching of joint capsule and soft tissue. Each stretch was sustained for 30-40 second and repeated in cyclic manner for 3 time per session. This mobilization treatment was applied parallel to routine physical therapy. All patients will be treated paralelly 3 time a week for 4 weeks.</i_keyword>
      <i_keyword>Group B will posterior shoulder sustained stretch glide. The patient will be in supine laying near the edge of treatment table. The therapist will distract the joint in open pack position and apply grade 3 stretch glide to posterior shoulder capsule. Each stretch will be sustained for 30-40 second. The treatment will be cyclically repeated for 3 time per session. All patients will be treated paralelly 3 time a week for 4 weeks.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Shouder Physical Disability. Timepoint: Evaluated before and after treatment. Method of measurement: Shoulder pain and disability index (SPADI).</prim_outcome>
      <prim_outcome>Shoulder pain intensity,. Timepoint: evaluated before and after treatment. Method of measurement: Numeric pain rating scale (NPRS),.</prim_outcome>
      <prim_outcome>Shoulder range of motion. Timepoint: evaluated before and after treatment. Method of measurement: Universal goniometer.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Thoracic Kyphosis Angle. Timepoint: evaluated before and after treatment protocol. Method of measurement: sagittal plane radiograph in weight bearing position and arm folded 45o.</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>2021-12-18</approval_date>
        <contact_name>Research ethics committee of Muhmmad Intitute of Medical and Allied Sciences</contact_name>
        <contact_address>HBL street Near Sabza Zar Metro Station, Bosan Road Multan Multan Punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
