<?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>IRCT20200611047734N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-06-22</date_registration>
      <primary_sponsor>king edward medical university,Lahore</primary_sponsor>
      <public_title>COMPARING THE EFFECT OF MUSCLE ENERGY TECHNIQUE AND MULLIGAN MOBILIZATION WITH MOVEMENT ON PAIN, RANGE OF MOTION AND DISABILTIY IN ADHESIVE CAPSULITIS</public_title>
      <acronym></acronym>
      <scientific_title>COMPARING THE EFFECT OF MUSCLE ENERGY TECHNIQUE AND MULLIGAN MOBILIZATION WITH MOVEMENT ON PAIN, RANGE OF MOTION AND DISABILTIY IN ADHESIVE CAPSULITIS</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-06-11</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>70</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/48851</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: Parallel groups, single blinded, single setting, Randomization description: it was a single blinded randomized control trial. in which participant were kept blind. All the participant who came to physiotherapy department was considered and screened for adhesive capsulitis stage 2 with having a restriction of movements. 70 patients were allotted in two groups i.e.; group A(MWM) and group B(MET) via lottery method, 35 in each group. Consider the inclusion and exclusion criteria before concerning them in study. Informed consent was taken whether they were willing to participate or not in written form, Blinding description: it was a single blinded study in which participant/ patients were kept blind for treatment technique. 2 different technique were provided to patients. and they were blind about that which technique was given   to which patients.</study_design>
      <phase>N/A</phase>
      <hc_freetext>adhesive Capsulitis stage 2.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Patient in A group was treated with Mulligan’s mobilization.Both groups were received the conventional therapy, which was remain same throughout the study. The conventional therapy includes hot pack for 10 minutes and shoulder exercises which include wand exercise, pulley rope, shoulder wheel exercise and wall climbing exercises.  Group A: -Application of hot pack, exercises and mulligan’s mobilization. 	Dosage: -   The glide was applied and sustained for approximately 5-10 s while the patient performed the pain-free gripping action. Totally, 6 repetitions of the technique were performed during a single treatment session. The period between each repetition was no longer than 60s. 	Duration: - Three session/week (alternative days) and treatment last for 3 weeks. Intervention 2: Intervention group: Patient in B group was treated with muscle energy technique.Both groups were received the conventional therapy, which was remain same throughout the study. The conventional therapy includes hot pack for 10 minutes and shoulder exercises which include wand exercise, pulley rope, shoulder wheel exercise and wall climbing exercises. 	Dosage: - Hold the position for 8-10and relax for 3-4 sec than gain new range. Totally, 6 repetitions of the technique were performed during a single treatment session. The period between each repetition was no longer than 60s.	Duration: 3 weeks with 3 sessions per 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:
COMPARING THE EFFECT OF MUSCLE ENERGY TECHNIQUE AND MULLIGAN MOBILIZATION WITH MOVEMENT ON PAIN, RANGE OF MOTION AND DISABILTIY IN ADHESIVE CAPSULITIS

When:
study is completed and become available after its publication

To whom:
person in academic institute. Patient data will not be shown .

Conditions:
under the usage with terms in which journal is accessed /processed for publication
it could be used in request.

Where to obtain:
+923367595206
from the University office and Responsible supervisor and from journal we will process in future

How to obtain:
can be on call or mail
It will be only used in confidential way for improving research and benefit of humanity

Comments:
data can bee provided on request</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>ayesha razzaq</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>sahar villa, boys multan public school road,Multan</address>
        <city>multan</city>
        <country1>Pakistan</country1>
        <zip>66000</zip>
        <telephone>+92 61 6521475</telephone>
        <email>drayesharazzak@gmail.com</email>
        <affiliation>king edward medical university,Lahore</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Rana Dilawaaiz Nadeem</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Neela Gumbadh, New Anarkali,Lahore</address>
        <city>Lahor</city>
        <country1>Pakistan</country1>
        <zip>36121</zip>
        <telephone>+92 42 99214819</telephone>
        <email>rdnadeem@yahoo.com</email>
        <affiliation>king edward Medical University,Lahore</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>	 Subject having stage 2 of frozen shoulder 	Age group 30-70years	Subject with bilateral/unilateral adhesive capsulitis	Both males and females	Subject who willing to participate</inclusion_criteria>
      <agemin>30 years</agemin>
      <agemax>70 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>	Malignancy	Patients was excluded if they exhibited	Subjects with Neuromuscular disorders 	Conditions that contraindicated to manual therapy.	Any participant who was unable to return for follow up treatment or evaluation. 	Any participant who received treatment concurrent to the research.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M75</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Shoulder lesions</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Devices</i_code>
      <i_code>Treatment - Devices</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Patient in A group was treated with Mulligan’s mobilization.Both groups were received the conventional therapy, which was remain same throughout the study. The conventional therapy includes hot pack for 10 minutes and shoulder exercises which include wand exercise, pulley rope, shoulder wheel exercise and wall climbing exercises.  Group A: -Application of hot pack, exercises and mulligan’s mobilization. 	Dosage: -   The glide was applied and sustained for approximately 5-10 s while the patient performed the pain-free gripping action. Totally, 6 repetitions of the technique were performed during a single treatment session. The period between each repetition was no longer than 60s. 	Duration: - Three session/week (alternative days) and treatment last for 3 weeks</i_keyword>
      <i_keyword>Intervention group: Patient in B group was treated with muscle energy technique.Both groups were received the conventional therapy, which was remain same throughout the study. The conventional therapy includes hot pack for 10 minutes and shoulder exercises which include wand exercise, pulley rope, shoulder wheel exercise and wall climbing exercises. 	Dosage: - Hold the position for 8-10and relax for 3-4 sec than gain new range. Totally, 6 repetitions of the technique were performed during a single treatment session. The period between each repetition was no longer than 60s.	Duration: 3 weeks with 3 sessions per weeks.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain. Timepoint: Baseline and after 3rd week. Method of measurement: Numeric Pain Rating Scale.</prim_outcome>
      <prim_outcome>Range of motion. Timepoint: baseline and after 3rd week. Method of measurement: Goniometer.</prim_outcome>
      <prim_outcome>Functional Disability. Timepoint: baseline and after 3rd week. Method of measurement: SPADI Tool.</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>academic support only</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-06-11</approval_date>
        <contact_name>Institutional Review Board</contact_name>
        <contact_address>Neela Gumbad,New Anarkali,Lahore Lahore punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
