<?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>IRCT201111025486N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2012-01-17</date_registration>
      <primary_sponsor>Tehran Unversity of Medical Sceinces - Vice Chancellor for Research</primary_sponsor>
      <public_title>A comparative study of exercise therapy and physiotherapy in improving shoulder pain, posture, muscle strength, flexibility and range of motion in patients  with shoulder overuse syndrome</public_title>
      <acronym>Exercise therapy &amp; Physical modalities in shoulder overuse syndrom</acronym>
      <scientific_title>A comparative study of exercise therapy and physiotherapy in improving shoulder pain, posture, muscle strength, flexibility and range of motion in patients  with shoulder overuse syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2012-01-01</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>70</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/5888</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Shoulder overuse syndrom.</hc_freetext>
      <i_freetext>Intervention 1: Intervention for group II or physical therapy group consist of  three days a week physical therapy during which the subjects treated with conventional TENS and ultrasound for 18 sessions (three sessions per week for 6 weeks) . Intervention 2: Exercise Therapy Group intervention :&#13;
 The exercise program will be done three days a week for 6 weeks. The exercise program is  included strengthening exercise, stretching ,proprioceptive and scapular stabilization exercise with swiss ball and Therabands.After 20 to 30 minute warm-up exercises will begin . In training sessions,  a series of stretching e xercises for the anterior muscles of the chest muscles and internal rotators of the shoulders are included.</i_freetext>
      <results_actual_enrolment></results_actual_enrolment>
      <results_date_completed></results_date_completed>
      <results_url_link></results_url_link>
      <results_summary>    Objectives: To determine the effect of exercise therapy on pain, posture, flexibility, shoulder mobility in patients with shoulder overuse syndrome in comparison with conventional physiotherapy.&lt;br /&gt;&#13;
&lt;br /&gt;&#13;
Method: The study was designed as a randomized clinical trial in 69 patients with shoulder overuse syndrome who were randomly assigned in two groups of exercise therapy (ET) (n=33) and physiotherapy (PT) (n=35). All participants received 18 sessions of exercise therapy or conventional physiotherapy. Pain, shoulders' range of abduction and external rotation, shoulder protraction, scapular rotation and symmetry as well as postural assessment including the forward shoulder and head, mid thoracic curvature and Pectoralis minor length were evaluated. All measurements were done pre and post intervention.&lt;br /&gt;&#13;
Results: Our findings indicate an increase in abduction and external rotation range, improvement the forward shoulder and increase in the shoulder flexibility of the involved shoulder in both groups but significant difference was observed in exercise therapy group. Pain reduction was showed in both groups and there was no significant difference between them. Protraction of the shoulder, forward head posture and mid thoracic curvature revealed a significant improvement in exercise therapy group.An apparent changes occurred in scapular rotation and symmetry in both groups but no significant differences were observed between them.&lt;br /&gt;&#13;
Conclusions:The findings of this study indicated in pain reduction, increasing of abduction and external rotation range, improvement of head , shoulder, scapula and mid thoracic posture and also increasing in involved shoulder flexibility after 6 weeks exercise therapy.&lt;br /&gt;&#13;
Keywords: Shoulder Overuse Syndromes, Posture, Exercise Therapy, Physiotherapy, Randomized Clinical Trial.&lt;br /&gt;&#13;
&lt;br /&gt;&#13;
       </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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Dr Azar Moezy</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Heamt Highway-Medicine school-Sports Medicine Deparment</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 21 8294 3424</telephone>
        <email>moeziazr@sina.tums.ac.ir</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr Azar Moezy</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Hemat Highway, Medicine School, Sports medicine department</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 21 8294 3424</telephone>
        <email>moeziazr@sina.tums.ac.ir</email>
        <affiliation>Teharn Unversity of Medical sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: unilateral or bilateral shoulder overuse syndrome based on patient’s history &amp; physical exams; age between 20 to50; normal mental state; no previous history of trauma &amp; acute injury; no previous history of shoulder surgery; no previous history of shoulder dislocation and no previous history of shoulder or arm fractures.&#13;
Exclusion criteria: patient’s unwilling to continue the study; diseases that impede patient to be attended in the study and absence in treatment sessions</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></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>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention for group II or physical therapy group consist of  three days a week physical therapy during which the subjects treated with conventional TENS and ultrasound for 18 sessions (three sessions per week for 6 weeks) .</i_keyword>
      <i_keyword>Exercise Therapy Group intervention :&#13;
 The exercise program will be done three days a week for 6 weeks. The exercise program is  included strengthening exercise, stretching ,proprioceptive and scapular stabilization exercise with swiss ball and Therabands.After 20 to 30 minute warm-up exercises will begin . In training sessions,  a series of stretching e xercises for the anterior muscles of the chest muscles and internal rotators of the shoulders are included.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain. Timepoint: Before intervention and six weeks after intervention. Method of measurement: Pain scale (VAS).</prim_outcome>
      <prim_outcome>Pectoralis minor length. Timepoint: Before intervention and six weeks after intervention. Method of measurement: Pectoralis minor length measurments.</prim_outcome>
      <prim_outcome>Shoulder Range of Motion. Timepoint: Before intervention and six weeks after intervention. Method of measurement: Goniometric measurement of shoulder Abduction and External rotation.</prim_outcome>
      <prim_outcome>Posture. Timepoint: Before intervention and six weeks after intervention. Method of measurement: Head, midthoracic, shoulder posture with measurement and calculations.</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>Tehran Unversity of Medical Sceinces - Vice Chancellor for Research</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2011-12-19</approval_date>
        <contact_name>Ethics committe of vice chancellor for research , TUMS</contact_name>
        <contact_address>Keshvarz Blvd Tehran  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
