<?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>IRCT20210121050099N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-01-25</date_registration>
      <primary_sponsor>Abbas Fadhil Taher</primary_sponsor>
      <public_title>Effects of Mulligan and Muscle Energy Techniques on Knee Osteoarthritis.</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of Effects of Mulligan Techniques and Muscle Energy Technique (MET) on Pain  and Function in Knee Osteoarthritis.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-01-19</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/53830</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The simple random allocation technique will be used to distribute those patients into a group of intervention; each subject has the opportunity to choose the intervention group randomly by pick up a small piece of paper out of 30 pieces (15 for MWM and 15 for MET) which contains the assigned interventions.</study_design>
      <phase>N/A</phase>
      <hc_freetext>chronic knee osteoarthritis.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group A: Mulligan mobilization with movement technique, physiotherapy manual exercises technique.       15 subjects in this group will have mulligan mobilization with movement in these different positions (prone and standing), according to pain laterality, plus conventional exercises therapy.           I. Subjects suffering from pain or more pain in the lateral aspect of the knee will receive the following intervention each session;      1)	lateral glide mobilization by using belt with active knee extension and flexion in prone position, 3 sets with 6 repetitions for extension and flexion in each set, 30 seconds rest between each set.          2) External rotation glide in standing position. with weight bearing and active knee flexion and extension The intervention continues with three sets of the MWM, of 6 repetitions in flexion and extension each set.         3)	conventional knee osteoarthritis exercises;  •Quadriceps isometric strengthening exercises; subject lay in supine position.  •	Straight leg raising exercise.   4)	 All of subjects will do home exercises program. This program includes conventional exercises such as quadriceps isometric strengthening, straight leg raising, hamstring curls-up and hip abduction exercises. Each exercise is done for 3 sets in each day with 30 repetitions and each repetition will last for 10 seconds muscle contraction period.                                                                                                  II.	Subjects suffering from pain in the medial aspect of the knee will receive the following intervention;1)	medial glide mobilization in prone position by using belt with active knee extension and flexion, 3 sets with 6 repetitions for extension and flexion each set, 30 seconds rest between each set. With similar above procedures. The only difference is the direction of gliding.                                                                                                   2)	Internal rotation in standing position with weight bearing and active knee flexion. The same procedure in I 2 with the difference in internal rotation gliding.    3) Conventional knee osteoarthritis exercises; quadriceps isometric strengthening exercises and straight leg raising Home active conventional osteoarthritis exercises. Intervention 2: Intervention group B: muscle energy manual exercises technique MET.  physiotherapy manual exercises technique. 15 subjects in this group will receive Post isometric relaxation of Muscle energy technique as following;           I.	Quadriceps MET contraction of quadriceps with only 20% of maximum voluntary contraction strength in extension against therapist’s resistance for 7-10 seconds, and followed by patient’s exhalation, the therapist stretches the muscle for 30 seconds. Then a new end position is found and ask the patient to repeat isometric contraction again, repeated this technique for 3-4 times.        II.Hamstring MET hold the hamstring isometric for 7-10 sec and followed by exhalation therapist stretch the muscle 30 second, to straighten the knee towards the new barrier. Repeating this technique until no further gain is possible (usually one or two repetitions achieve the maximum degree of lengthening available at any one session) for 3-4 time.        III. Tensor fascia lata (TFL)  MET	Patient asked to abduct leg against resistance (using less than a 25% strength, slowly take your leg back towards the midline, against my resistance).•	After contraction ceases, and patient relaxes, during patient’s exhalation, the leg should be taken to or through the new restriction barrier (into adduction past the barrier) to stretch the muscular fibers of TFL (the upper third structure).•	Care taken to ensure that pelvis is not tilted during stretch.•	Stability is achieved by therapist pressure maintained against flexed knee/thigh.•	Entire process should be repeated several times or until no further gain is possible            IV.	Conventional osteoarthritis exercises (quadriceps isometric strengthening sets and straight leg raising exercises).V.	All of patients will do home exercises program. This program includes conventional exercises such as quadriceps isometric strengthening, straight leg raising, hamstring curls-up and hip abduction exercises. Each exercise is done for 3 sets in each day with 30 repetitions and each repetition will last for  10 seconds muscle contraction period.</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 not yet</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Abbas Taher</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Enghilab</address>
        <city>Tehran</city>
        <country1>Iraq</country1>
        <zip>76984</zip>
        <telephone>+964 21 058 3318</telephone>
        <email>abasfq@gmail.com</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Abbas Taher</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Enghilab</address>
        <city>Tehran</city>
        <country1>Iraq</country1>
        <zip>76984</zip>
        <telephone>+964 21 058 3318</telephone>
        <email>abasfq@gmail.com</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iraq</country2>
    </countries>
    <criteria>
      <inclusion_criteria>•	Patients with Chronic unilateral (preferably) or bilateral (intervention will be to dominant side) knee osteoarthritis confirmed by x-ray, Without ligament pathology or injury (grade II and grade III of Kellegren and Lawrence classification).(50)
•	patients are independently mobile.
•	BMI must be ≤ 30.
•	Visual Analogue Scale must be ≥4
•	Knee Extension lack ≥20 degrees
•	Willingness to participate and follow the treatment schedule.
•	Patients will be in study if they have no concomitant disease affecting the knee, e.g. rheumatoid arthritis, recent injury, and/or surgery to the knee and had received intra- articular corticosteroid during the last 6 months</inclusion_criteria>
      <agemin>35 years</agemin>
      <agemax>60 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>•	Absent for two or more continuous sessions.
•	Patients who have pathological fractures, revision surgeries, associated ipsilateral injuries, and neurovascular disorders will be excluded from the study.
Patients who are not satisfied to continue the treatment.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M17</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Osteoarthritis of knee</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group A: Mulligan mobilization with movement technique, physiotherapy manual exercises technique.       15 subjects in this group will have mulligan mobilization with movement in these different positions (prone and standing), according to pain laterality, plus conventional exercises therapy.           I. Subjects suffering from pain or more pain in the lateral aspect of the knee will receive the following intervention each session;      1)	lateral glide mobilization by using belt with active knee extension and flexion in prone position, 3 sets with 6 repetitions for extension and flexion in each set, 30 seconds rest between each set.          2) External rotation glide in standing position. with weight bearing and active knee flexion and extension The intervention continues with three sets of the MWM, of 6 repetitions in flexion and extension each set.         3)	conventional knee osteoarthritis exercises;  •Quadriceps isometric strengthening exercises; subject lay in supine position.  •	Straight leg raising exercise.   4)	 All of subjects will do home exercises program. This program includes conventional exercises such as quadriceps isometric strengthening, straight leg raising, hamstring curls-up and hip abduction exercises. Each exercise is done for 3 sets in each day with 30 repetitions and each repetition will last for 10 seconds muscle contraction period.                                                                                                  II.	Subjects suffering from pain in the medial aspect of the knee will receive the following intervention;1)	medial glide mobilization in prone position by using belt with active knee extension and flexion, 3 sets with 6 repetitions for extension and flexion each set, 30 seconds rest between each set. With similar above procedures. The only difference is the direction of gliding.                                                                                                   2)	Internal rotation in standing position with weight bearing and active knee flexion. The same procedure in I 2 with the difference in internal rotation gliding.    3) Conventional knee osteoarthritis exercises; quadriceps isometric strengthening exercises and straight leg raising Home active conventional osteoarthritis exercises.</i_keyword>
      <i_keyword>Intervention group B: muscle energy manual exercises technique MET.  physiotherapy manual exercises technique. 15 subjects in this group will receive Post isometric relaxation of Muscle energy technique as following;           I.	Quadriceps MET contraction of quadriceps with only 20% of maximum voluntary contraction strength in extension against therapist’s resistance for 7-10 seconds, and followed by patient’s exhalation, the therapist stretches the muscle for 30 seconds. Then a new end position is found and ask the patient to repeat isometric contraction again, repeated this technique for 3-4 times.        II.Hamstring MET hold the hamstring isometric for 7-10 sec and followed by exhalation therapist stretch the muscle 30 second, to straighten the knee towards the new barrier. Repeating this technique until no further gain is possible (usually one or two repetitions achieve the maximum degree of lengthening available at any one session) for 3-4 time.        III. Tensor fascia lata (TFL)  MET	Patient asked to abduct leg against resistance (using less than a 25% strength, slowly take your leg back towards the midline, against my resistance).•	After contraction ceases, and patient relaxes, during patient’s exhalation, the leg should be taken to or through the new restriction barrier (into adduction past the barrier) to stretch the muscular fibers of TFL (the upper third structure).•	Care taken to ensure that pelvis is not tilted during stretch.•	Stability is achieved by therapist pressure maintained against flexed knee/thigh.•	Entire process should be repeated several times or until no further gain is possible            IV.	Conventional osteoarthritis exercises (quadriceps isometric strengthening sets and straight leg raising exercises).V.	All of patients will do home exercises program. This program includes conventional exercises such as quadriceps isometric strengthening, straight leg raising, hamstring curls-up and hip abduction exercises. Each exercise is done for 3 sets in each day with 30 repetitions and each repetition will last for  10 seconds muscle contraction period.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Patients' opinion about thier knees. Timepoint: before first session, after third one and 4 weeks after the last session. Method of measurement: Knee Injury and Osteoarthritis Outcome Score (KOOS) Arabic version (Questionnaire).</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>Abbas Fadhil Taher</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-01-18</approval_date>
        <contact_name>Tehran university medical sciences. Ethics Committee of Nursing Midwifery and rehabilitation.</contact_name>
        <contact_address>enghilab tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
