<?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>IRCT20190315043058N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-01-09</date_registration>
      <primary_sponsor>Iran University of Medical Sciences</primary_sponsor>
      <public_title>The effects of Mobilization with movement technique and knee osteoarthritis conventional physiotherapy in knee osteoarthritis.</public_title>
      <acronym></acronym>
      <scientific_title>The effects of Mobilization with movement technique and knee osteoarthritis conventional physiotherapy on disability, pain and spatiotemporal and kinematic characteristics of gait in individuals with knee osteoarthritis</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-01-29</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>38</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/74818</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Factorial, Purpose: Treatment, Randomization description: Subjects will be divided into two control and treatment groups by the stratified randomization method, so the two groups will be balanced in terms of gender, and the process of this random division will be such that after creating blocks of 4 in each class (male gender and female) which consist of letters A and B, we will create a random sequence of these blocks using RANDOM NUMBER GENERATOR and the subjects will be placed in two control and treatment groups based on the order of reference by this sequence. The individual generating the randomization sequence will not participate in any other phase of the study, Blinding description: In this study, the examiner or the person in charge of data collection and the one who evaluates the outcome and the subject or the participant will not know how the groups are divided. The examiner will not be present at the stage of dividing the subjects into treatment and control groups and the rest of the study stages. Also, the treatment that the subjects will receive in both groups will be apparently  and look the same. In the treatment group, the subjects will receive preparatory treatments, therapeutic exercises and manual treatments in the form of the Mulligan technique, and in the control group, the subjects will receive preparatory treatments, therapeutic exercises and manual treatments in the form of the Mulligan technique in a simulated form; The method of performing this technique will be in such a way that no force will be applied to the place of handing after correct handing.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Knee Osteoarthritis.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Intervention group: The participants in this group will receive10 treatment sessions during 4 weeks with at least one day between sessions by a therapist who is proficient in the Mulligan technique and regular physical therapy. The treatment in each group lasts for 60 minutes and includes 3 phases of preparation, exercise therapy and manual treatments. The first phase, preparation: in this phase, subjects will receive high-frequency electrical nerve surface stimulation for 20 minutes and infra red for 15 minutes. 4 electrodes are placed inside wet pads around the knee joint (two electrodes on the medial of the knee above and below the joint line and two electrodes on the lateral of the knee above and below the joint line) and will be tightened by the strap. The frequency and pulse duration used will be 110 Hz and 50 microseconds, respectively. The second phase, exercise therapy: The exercise therapy  for these people will be in the form of strengthening exercises, stretching exercises, and range of motion exercises. Strengthening exercises include isotonic contraction with the help of varying leg weights of the knee extensor and hip abductor muscles, respectively, in sitting positions on the edge of the bed and lying on the side while the painful knee is elevated, with a frequency of 3 sessions per week according to the ability of the subject with The intensity of 60% to 80% of 1RM will include 2 to 4 sets of 8 to 15 sets, and between each set we will allocate 30 to 60 seconds of rest time to the subjects. We will use stretching exercises and active range exercises for muscle shortening or reducing the range of motion that disrupts the person's performance. Stretching exercises will be performed for 30 seconds in 3 sets of 10 for the biceps and hamstring muscles, and active and passive range of motion exercises will be performed in the form of movement from fully bent knee to fully straightened knee in 3 sets of 10. will get The third phase, manual treatments: At first, we will perform these exercises while lying on the back with the knees slightly bent. If the subject does not have pain in bending or straightening the knee while lying on the back, we will perform this technique for the subject while standing. gave Also, if after a few treatment sessions, the examiner does not have pain in bending and straightening his knee while lying on his back, we will follow the technique while standing. The treatment process will be like this, lying on the back with a slightly bent knee, we will ask the subject to actively bend and straighten the knee, then after placing hands around the knee joint, the subject's leg will be internally rotated, respectively. We will perform external rotation, internal glide, external glide, anterior glide and posterior glide and at the same time we will ask the subject to move his knee in the same painful direction and if the active movement of the subject that was painful before with any of the rotations or glides It was done without pain, we will use the same rotation or glide to continue the treatment. This technique should be performed without pain or with minimal pain, and if the pain decreases but does not reach zero, the therapist will reach a completely pain-free state by increasing or decreasing the applied pressure or applying additional pressure at the end of the range. This technique will be performed in the first session as a set of 6 and in the following sessions, according to the subject's ability, as 3 to 5 sets of 6 to 10. To perform the technique in a standing position, the subject will place the sole of the foot whose knee is painful on a stool at a height of 30 cm ; Then we will take active knee bending and straightening movements by applying internal and external rotations, internal and external glides, and anterior and posterior glides to the subject's leg. If the rotations do not hurt, we will continue the painful movement with the same rotation or glide for the subject. Secondary intervention description: After completion 10 sessions of the physiotherapy intervention, participants will be re-randomized, such that an equal number of participants from each group will be allocated to the intervention and control groups. In this study, the knee joint with more severe symptoms will be selected for assessment of muscle activation and fitting of the unloader knee brace. In cases where symptom severity is equal in both knees, the dominant knee will be selected. Both groups will use the brace daily for 1 to 8 hours and will perform twelve 30-minute walking sessions over a four-week period. The control group will use the unloader knee brace without electrical stimulation, whereas the NMES group will receive neuromuscular electrical stimulation concurrently with gait during walking. Stimulation intensity will be adjusted based on patient feedback up to the maximum tolerable level, such that painless muscle contractions are elicited, and participants will be encouraged to gradually increase the stimulation intensity. Electrode placement will be instructed by a physiotherapist, and patient adherence will be monitored through weekly follow-ups and adherence forms. Intervention 2: Control group: Intervention group: Intervention group: The participants in this group will receive10 treatment sessions during 4 weeks with at least one day between sessions by a therapist who is proficient in the Mulligan technique and regular physical therapy. The treatment in each group lasts for 60 minutes and includes 3 phases of preparation, exercise therapy and artificial manual treatments . The first phase, preparation: in this phase, subjects will receive high-frequency electrical nerve surface stimulation for 20 minutes and infra red for 15 minutes. 4 electrodes are placed inside wet pads around the knee joint (two electrodes on the medial of the knee above and below the joint line and two electrodes on the lateral of the knee above and below the joint line) and will be tightened by the strap. The frequency and pulse duration used will be 110 Hz and 50 microseconds, respectively. The second phase, exercise therapy: The exercise therapy  for these people will be in the form of strengthening exercises, stretching exercises, and range of motion exercises. Strengthening exercises include isotonic contraction with the help of varying leg weights of the knee extensor and hip abductor muscles, respectively, in sitting positions on the edge of the bed and lying on the side while the painful knee is elevated, with a frequency of 3 sessions per week according to the ability of the subject with The intensity of 60% to 80% of 1RM will include 2 to 4 sets of 8 to 15 sets, and between each set we will allocate 30 to 60 seconds of rest time to the subjects. We will use stretching exercises and active range exercises for muscle shortening or reducing the range of motion that disrupts the person's performance. Stretching exercises will be performed for 30 seconds in 3 sets of 10 for the biceps and hamstring muscles, and active and passive range of motion exercises will be performed in the form of movement from fully bent knee to fully straightened knee in 3 sets of 10.The third phase, manual treatments: after the usual physical therapy exercises, the Mulligan technique will be performed in an artificial way for these patients in such a way that hands will be placed around the joint and the subject will be asked to bend and straighten his knee without applying  glide or pressure, and we will perform this operation in 3 to 5 sets of 6 to 10, and we will give the patient a 60-second rest between each set. All the mentioned steps, including the evaluation to find the glide or rotation with pain-free movement, as well as the part of performing the technique for the treatment, for the implementation of this technique in the treatment group, will be done exactly for the control group, and as it was said, the only difference will be this. It was that the glide or rotation in question will not be done in real way and no force will be applied and it will only be manual.</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 further information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Hanieh Javan</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Hanieh Javan.Unit 7, No 39, Alidoosti St, Ahaniamineh Ave, Tehran Pars</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1653874986</zip>
        <telephone>+98 21 7788 9173</telephone>
        <email>javan.h@iums.ac.ir</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Esmaeil Ebrahimi Takamjani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Rehabilitation Sciences, Iran University of Medical Sciences, Shah Nazari St., Maddkaran St., Mader Square, Mirdamad, Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۱۳۴۸۷ ۱۵۴۵۹</zip>
        <telephone>+98 21 2222 8051</telephone>
        <email>ebrahimitakamjani.e@iums.ac.ir</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>1) Age 40 to 70 years
2) Diagnosis of knee tibiofemoral joint arthrosis based on the criteria of the American College of Rheumatology (knee pain for at least the last 3 months, joint crepitation and morning stiffness lasting 30 minutes or less) by a specialist physician.
3) Pain intensity based on visual pain scale between 4 and 8 while walking at the time of evaluation
4) The severity of arthritis should be 2 and 3 based on the Kellgren and Lawrence classification system.
5) Ability to walk more than 6 meters
6) One-sided arthritis pain of the tibiofemoral joint of the knee (even if a person has bilateral arthritis, a knee that is painful will be included in the study)
7) Having knee pain for more than 3 months</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>70 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>1) Any neurological problem that affects a person's walking, such as a stroke
2) Arthritis secondary to trauma or accident or fracture in the joint
3) Any surgery and fracture in any of the lower limbs in the last year
4) Injection of corticosteroid or hyaluronic acid or platelet-rich plasma in the last 6 months
5) Any pain in the upper or lower joints
6) Heart problems with medium and high risk, such as uncontrolled angina or heart infarction in the last month
7) Inflammation and infection in the knee
8) Any prohibition to manual treatments such as severe osteoporosis or unstable joint
9) Cognitive problem
10) Receiving physiotherapy intervention for knee arthritis in the last 12 months
11) Body mass index above 35
12) Using walking aids
13) Smoking
14) Systemic diseases such as rheumatoid arthritis</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></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>Intervention group: Intervention group: The participants in this group will receive10 treatment sessions during 4 weeks with at least one day between sessions by a therapist who is proficient in the Mulligan technique and regular physical therapy. The treatment in each group lasts for 60 minutes and includes 3 phases of preparation, exercise therapy and manual treatments. The first phase, preparation: in this phase, subjects will receive high-frequency electrical nerve surface stimulation for 20 minutes and infra red for 15 minutes. 4 electrodes are placed inside wet pads around the knee joint (two electrodes on the medial of the knee above and below the joint line and two electrodes on the lateral of the knee above and below the joint line) and will be tightened by the strap. The frequency and pulse duration used will be 110 Hz and 50 microseconds, respectively. The second phase, exercise therapy: The exercise therapy  for these people will be in the form of strengthening exercises, stretching exercises, and range of motion exercises. Strengthening exercises include isotonic contraction with the help of varying leg weights of the knee extensor and hip abductor muscles, respectively, in sitting positions on the edge of the bed and lying on the side while the painful knee is elevated, with a frequency of 3 sessions per week according to the ability of the subject with The intensity of 60% to 80% of 1RM will include 2 to 4 sets of 8 to 15 sets, and between each set we will allocate 30 to 60 seconds of rest time to the subjects. We will use stretching exercises and active range exercises for muscle shortening or reducing the range of motion that disrupts the person's performance. Stretching exercises will be performed for 30 seconds in 3 sets of 10 for the biceps and hamstring muscles, and active and passive range of motion exercises will be performed in the form of movement from fully bent knee to fully straightened knee in 3 sets of 10. will get The third phase, manual treatments: At first, we will perform these exercises while lying on the back with the knees slightly bent. If the subject does not have pain in bending or straightening the knee while lying on the back, we will perform this technique for the subject while standing. gave Also, if after a few treatment sessions, the examiner does not have pain in bending and straightening his knee while lying on his back, we will follow the technique while standing. The treatment process will be like this, lying on the back with a slightly bent knee, we will ask the subject to actively bend and straighten the knee, then after placing hands around the knee joint, the subject's leg will be internally rotated, respectively. We will perform external rotation, internal glide, external glide, anterior glide and posterior glide and at the same time we will ask the subject to move his knee in the same painful direction and if the active movement of the subject that was painful before with any of the rotations or glides It was done without pain, we will use the same rotation or glide to continue the treatment. This technique should be performed without pain or with minimal pain, and if the pain decreases but does not reach zero, the therapist will reach a completely pain-free state by increasing or decreasing the applied pressure or applying additional pressure at the end of the range. This technique will be performed in the first session as a set of 6 and in the following sessions, according to the subject's ability, as 3 to 5 sets of 6 to 10. To perform the technique in a standing position, the subject will place the sole of the foot whose knee is painful on a stool at a height of 30 cm ; Then we will take active knee bending and straightening movements by applying internal and external rotations, internal and external glides, and anterior and posterior glides to the subject's leg. If the rotations do not hurt, we will continue the painful movement with the same rotation or glide for the subject. Secondary intervention description: After completion 10 sessions of the physiotherapy intervention, participants will be re-randomized, such that an equal number of participants from each group will be allocated to the intervention and control groups. In this study, the knee joint with more severe symptoms will be selected for assessment of muscle activation and fitting of the unloader knee brace. In cases where symptom severity is equal in both knees, the dominant knee will be selected. Both groups will use the brace daily for 1 to 8 hours and will perform twelve 30-minute walking sessions over a four-week period. The control group will use the unloader knee brace without electrical stimulation, whereas the NMES group will receive neuromuscular electrical stimulation concurrently with gait during walking. Stimulation intensity will be adjusted based on patient feedback up to the maximum tolerable level, such that painless muscle contractions are elicited, and participants will be encouraged to gradually increase the stimulation intensity. Electrode placement will be instructed by a physiotherapist, and patient adherence will be monitored through weekly follow-ups and adherence forms.</i_keyword>
      <i_keyword>Control group: Intervention group: Intervention group: The participants in this group will receive10 treatment sessions during 4 weeks with at least one day between sessions by a therapist who is proficient in the Mulligan technique and regular physical therapy. The treatment in each group lasts for 60 minutes and includes 3 phases of preparation, exercise therapy and artificial manual treatments . The first phase, preparation: in this phase, subjects will receive high-frequency electrical nerve surface stimulation for 20 minutes and infra red for 15 minutes. 4 electrodes are placed inside wet pads around the knee joint (two electrodes on the medial of the knee above and below the joint line and two electrodes on the lateral of the knee above and below the joint line) and will be tightened by the strap. The frequency and pulse duration used will be 110 Hz and 50 microseconds, respectively. The second phase, exercise therapy: The exercise therapy  for these people will be in the form of strengthening exercises, stretching exercises, and range of motion exercises. Strengthening exercises include isotonic contraction with the help of varying leg weights of the knee extensor and hip abductor muscles, respectively, in sitting positions on the edge of the bed and lying on the side while the painful knee is elevated, with a frequency of 3 sessions per week according to the ability of the subject with The intensity of 60% to 80% of 1RM will include 2 to 4 sets of 8 to 15 sets, and between each set we will allocate 30 to 60 seconds of rest time to the subjects. We will use stretching exercises and active range exercises for muscle shortening or reducing the range of motion that disrupts the person's performance. Stretching exercises will be performed for 30 seconds in 3 sets of 10 for the biceps and hamstring muscles, and active and passive range of motion exercises will be performed in the form of movement from fully bent knee to fully straightened knee in 3 sets of 10.The third phase, manual treatments: after the usual physical therapy exercises, the Mulligan technique will be performed in an artificial way for these patients in such a way that hands will be placed around the joint and the subject will be asked to bend and straighten his knee without applying  glide or pressure, and we will perform this operation in 3 to 5 sets of 6 to 10, and we will give the patient a 60-second rest between each set. All the mentioned steps, including the evaluation to find the glide or rotation with pain-free movement, as well as the part of performing the technique for the treatment, for the implementation of this technique in the treatment group, will be done exactly for the control group, and as it was said, the only difference will be this. It was that the glide or rotation in question will not be done in real way and no force will be applied and it will only be manual.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Disability score in Western Ontario and McMaster Universities Osteoarthritis Index  questionnaire. Timepoint: Measurement of Western Ontario and McMaster Universities Osteoarthritis Index  questionnaire score at the beginning of the study and after 10 sessions of physiotherapy treatment. Method of measurement: Western Ontario and McMaster Universities Osteoarthritis Index.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Spatiotemporal and Kinematic characteristics of gait. Timepoint: Measurement of spatio-temporal and kinematic parameters of walking at the beginning of the study and after 10 sessions of physiotherapy treatment. Method of measurement: Vicon Motion Capture System.</sec_outcome>
      <sec_outcome>Intensity of pain. Timepoint: Measurement of intensity of pain at the beginning of the study and after 10 sessions of physiotherapy treatment. Method of measurement: Visual Analogue Scale.</sec_outcome>
      <sec_outcome>Characteristics of electromyographic activity of muscles during gait, sit to stand and static balance. Timepoint: Measurement of variables at the beginning of the study and after 10 sessions of physiotherapy treatment and after 12 sessions of home-based walking training. Method of measurement: Kistler force plates and Myon electromyography system.</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>Iran University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-10-23</approval_date>
        <contact_name>Ethics committee of Iran University of Medical Sciences</contact_name>
        <contact_address>Iran University of Medical Sciences, Hemet Highway, next to Milad Tower, Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-10-29</approval_date>
        <contact_name>Ethics committee of Iran University of Medical</contact_name>
        <contact_address>Iran University of Medical Sciences, Hemet Highway, next to Milad Tower, Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
