<?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>IRCT20181024041444N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-02-16</date_registration>
      <primary_sponsor>The University Of Kharazmi</primary_sponsor>
      <public_title>The effect Movement-Pattern Training on pain، muscle activity response and selected landing kinematic variables</public_title>
      <acronym></acronym>
      <scientific_title>The effect Movement-Pattern Training on pain، muscle activity response and selected landing kinematic variables in  people with Non-specific chronic low back pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-05-20</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/34745</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Simple randomization
Following the initial screening and collection of labs, all study subjects started therapy within 3 days of baseline measurements. A study investigator, who did not perform any clinical measurements on study subjects, used a coin-flip to randomly assign study subjects to either the experimental control groups, Blinding description: Data Analyzer were blind before and after the experiment.In a way that did not explain to them which control group and which experimental group.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Low back pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: All the intervention group underwent a total of 21 supervised training sessions,over a 6-week period The MPT program incorporated 2 primary components,including (1) task-specific training for basic functional tasks 6 supervised in the week 1 For the task-specific training, all patients received standard instructions, to optimize their movement pattern during basic dailytasks, such as ascending stairs and sit to stand.(2):2-6 weeks:Strengthen thigh muscles. Intervention 2: Control group: Normal daily activity.</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:
Intervention program protocol file and data analysis information through publication in dissertation or article writing

When:
Access period starts 6 months after the results are published

To whom:
The research team of this study and other scientific and clinical researchers who do research for the benefit of these patients

Conditions:
Researchers who intend to use data in writing a meta-analysis or systematic article

Where to obtain:
afshiinorouji@gmail.com

How to obtain:
Their request will be answered after the approval of the academic institution

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Amirali jafarneghad gero</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>university Blvd</address>
        <city>Ardabil</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5616693595</zip>
        <telephone>+98 45 3335 6401</telephone>
        <email>amiralijafarnezhad@gmail.com‏</email>
        <affiliation>The University of Mohagheghe Ardabili</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Amiralijafarneghadgero</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>University Blvd</address>
        <city>Ardabil</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5616693595</zip>
        <telephone>+98 45 3335 6401</telephone>
        <email>amiralijafarnezhad@gmail.com‏</email>
        <affiliation>The University of  Mohagheghe Ardabili</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Low back pain for more than 3 months</inclusion_criteria>
      <agemin>8 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>spondylolisthesis or spondylolysis
ankylosing spondylitis
moderate to severe spinal osteoarthritis,
inflammatory arthritis
physically active
nerve root compression
trunk neuromuscular disease
scoliosis (15˚ or more)
previous spinal surgery, malignant tumour
hypertension
degenerative or inflammatory diseases of the lumbar spine</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>کمردرد</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: All the intervention group underwent a total of 21 supervised training sessions,over a 6-week period The MPT program incorporated 2 primary components,including (1) task-specific training for basic functional tasks 6 supervised in the week 1 For the task-specific training, all patients received standard instructions, to optimize their movement pattern during basic dailytasks, such as ascending stairs and sit to stand.(2):2-6 weeks:Strengthen thigh muscles.</i_keyword>
      <i_keyword>Control group: Normal daily activity</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Visual Analogue Scale. Timepoint: Before intervention، after 45 days after intervention، 45 days after the intervention. Method of measurement: Pain   Quebeck Questionnaire.</prim_outcome>
      <prim_outcome>Landing degree. Timepoint: Before intervention، after 45 days after intervention،45 days after the intervention. Method of measurement: Electrogoniametr.</prim_outcome>
      <prim_outcome>Muscle response. Timepoint: Before intervention، after 45 days after intervention،45 days after the intervention. Method of measurement: Electromyography.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Intervention group: The movement pattern exercises are taught in the first week of the correct training of movements in everyday activities, including walking, sitting, standing, walking up and down, and proper daily routine exercises, and from the second to the fourth week of the boost muscle, each The exercises have 5 steps from easy to hard. If you do not have a feeling of pain, you should do the 4 th and 5 th steps using Teraband, which include (20 to 10 repetitions of 2 sets), the second week to strengthen the flexors, Third week strengthen the extensor muscles of the thigh, fourth week strengthen muscle of the abductor, fifth week, strengthen the muscles of the catheter, And the sixth week to strengthen the complexion of the thigh muscles. Timepoint: After the test steps for 45 days. Method of measurement: Movement pattern training.</sec_outcome>
      <sec_outcome>Without intervention - Based on ethics in research after the end of interventions for  such as intervention group. Timepoint: For 45 days after the end of the interventions. Method of measurement: Movement pattern training.</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>The University Of Kharazmi</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-06-23</approval_date>
        <contact_name>Ethics committee of shahid beheshti University</contact_name>
        <contact_address>Tehran -  Ghods Town (West), between South Flamek and Zarafshan, Iran TV St. - Headquarters of the Ministry of Health, Treatment and Medical Education, Block A, 13th floor Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
