<?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>IRCT20211101052934N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-03-09</date_registration>
      <primary_sponsor>Semnan University of Medical Sciences</primary_sponsor>
      <public_title>Comparison of mobilization and mobilization with movement on acromiohumeral distance in athletes with shoulder primary impingement syndrome</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of therapeutic effects of mobilization and mobilization with movement on acromiohumeral distance in athletes with shoulder primary impingement syndrome: A randomized clinical trial</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-12-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>51</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/59737</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: .In this study, we use the randomized permutation block method for random assignment. The operation will be as follows: three and six blocks with a combination of A (mobilization), B (motion mobilization) and C (control) will be the criteria. Depending on the different combinations, each of the blocks is assigned a number as follows:
Block 1: BCAACB
Block 2: BAACCB
Block 3: ABC
Block 4: ACBCAB
Block 5: CBABCA
Block 6: ABBCAC
Block 7: ABBACC
Block 8: ACBBAC
Block 9: CBA
Block 10: ABCACB                                                                    
Using a table of random numbers, considering the numbers 1 to 9 in the unit and considering the number zero as the tenth block, select the order of the blocks and how to assign patients to one of the groups A, B or C according to the selected blocks of the face. Takes. After preparing a randomization list for each patient, they will have a number in the order of enrollment (from 1 to 51). A sealed envelope is provided with A, B, or C written inside the envelope based on the compiled list. The researcher who does not know the main list, after registering the person entered to study and check the number of the person, opens the relevant envelope and realizes the type of intervention based on the contents of the envelope.In this way, the researcher realizes the type of intervention only after the patient enters the study and determines her eligibility, by opening the envelope, and finally we will have three balanced groups, Blinding description: Participants are divided into three groups by general matching and randomly using random and double-blind blocking methods. Participants and evaluators do not know the division. All evaluations and measurements of the results are performed by an experienced person who has no knowledge of grouping individuals. The control group will receive each of the desired treatments within two weeks of their choice.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Primary Shoulder impingement syndrome.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Mobilization exercises (mobilization) for 6 sessions (3 times a week). In this group, mobilization techniques for the glenohumeral joint are performed by a training therapist and individuals three times a week for 3 weeks under his supervision. Are treated (21) .Then in each person four separate techniques including Inferior glide, posterior glide, anterior glide and lateral glide are used (Figure 1). The physiotherapist applies oscillating pressure for 2 to 3 oscillations per second. Grade III and IV apply. Each technique is performed 4 times (30 seconds each) (21). Intervention 2: Intervention group: In this group, the patient sits at the edge of the table. The patient's arms should rotate outward while performing the abduction. The therapist stands behind the patient on the healthy shoulder and holds the scapular with one hand. The protrusion of the other hand is located on the anterior part of the head of Homer (Figure 2) (48). Motion Animation (MVM) for 6 sessions (3 times a week): Three sets consisting of 10 repetitions and each repetition takes 4 seconds (Figure 2). For each person, the mobilization technique is used as Inferior, posterior, anterior and lateral (14,38). Intervention 3: Control group:  The control group does not receive any intervention for 2 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>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 more information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Zohreh Shokrian Tosi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Farhang 8 Alley, Farhang Street</address>
        <city>Sari</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>48186-15375</zip>
        <telephone>+98 11 3332 5586</telephone>
        <email>zohreh_sh_pt@hotmail.com</email>
        <affiliation>Semnan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Zohreh Shokrian Tosi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Farhang 8 Alley, Farhang Street</address>
        <city>Sari</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>48186-15375</zip>
        <telephone>+98 11 3332 5586</telephone>
        <email>zohreh_sh_pt@hotmail.com</email>
        <affiliation>Semnan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age between 20 to 35 years
Semi-professional athletes (who exercise an average of 3 to 6 hours per week)
Doing overhead exercises such as volleyball
primary impingement syndrome of shoulder
Patient consent to participate in the study</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>35 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>History of trauma, fracture, dislocation or surgery in the neck and shoulders
Osteoporosis
Tumor or neuromuscular disorders around the shoulder
Any subcutaneous inflammation
Inflammatory disorders such as rheumatoid arthritis
Adhesive capsules
Complete rupture of the rotator cuff tendon
Corticosteroid injections in shoulders in the past year
Received physical therapy for the shoulder or spine in the last 3 months</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>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Mobilization exercises (mobilization) for 6 sessions (3 times a week). In this group, mobilization techniques for the glenohumeral joint are performed by a training therapist and individuals three times a week for 3 weeks under his supervision. Are treated (21) .Then in each person four separate techniques including Inferior glide, posterior glide, anterior glide and lateral glide are used (Figure 1). The physiotherapist applies oscillating pressure for 2 to 3 oscillations per second. Grade III and IV apply. Each technique is performed 4 times (30 seconds each) (21).</i_keyword>
      <i_keyword>Intervention group: In this group, the patient sits at the edge of the table. The patient's arms should rotate outward while performing the abduction. The therapist stands behind the patient on the healthy shoulder and holds the scapular with one hand. The protrusion of the other hand is located on the anterior part of the head of Homer (Figure 2) (48). Motion Animation (MVM) for 6 sessions (3 times a week): Three sets consisting of 10 repetitions and each repetition takes 4 seconds (Figure 2). For each person, the mobilization technique is used as Inferior, posterior, anterior and lateral (14,38).</i_keyword>
      <i_keyword>Control group:  The control group does not receive any intervention for 2 weeks.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Acromiohumeral distance (AHD). Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: AHD measurement method using ultrasonography.</prim_outcome>
      <prim_outcome>Functional Status and Symptom Severity of shoulder. Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: Using Shoulder Pain and Disability Index (SPADI).</prim_outcome>
      <prim_outcome>Pain severity. Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: Visual Analogues Scale (VAS).</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>Semnan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-10-26</approval_date>
        <contact_name>Research Ethics Committees of Semnan University Of Medical Sciences</contact_name>
        <contact_address>Semnan University of Medical Sciences and Health Services, Basij Blvd. Semnan Semnan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
