<?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>IRCT20190225042842N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2019-09-30</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>Effectiveness of core stability Training of Lumbar Muscles in patients with Acute Low Back Pain</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of core stability Training of Lumbar Muscles in brucellosis Patients with Acute Low Back Pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-04-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/38104</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: In the present study, a sample size of approximately 24 people, 12 balls for intervention group A and 12 balls for intervention group B were placed in a lottery container and then the balls were randomly removed from the container without replacement and the resulting sequence was recorded.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Low back pain in patients with brucellosis.</hc_freetext>
      <i_freetext>Intervention 1: Stabilization Exercise Group Exercise Program: In this group, the sample will perform training sessions in 42 sessions under the supervision of a sports medicine specialist and physical education expert, in 3 sessions per day for 2 weeks in each session for approximately 10 minutes. At the beginning of each treatment session, a warm-up (about 5 minutes) will consist of light stretching exercises and each exercise will be repeated in 3 sets. The overload and incremental increase of each exercise will be monitored and determined with respect to the correct execution and pressure of the exercise in the previous session. The goal is to maximize the repetitions of each exercise per set. The major emphasis will be on the multifidus and transverse abdominal muscles. All movements should be performed ten times in painless range. Ten minutes in the morning, ten minutes in the afternoon and ten minutes in the evening. Intervention group: Patients with low back pain will undergo core stability training called core stability training. 2 to 3 times and 10 times each. Repeat the first move: the person pulls the legs up and down in a cramped position while the legs are rotating. The second move: back and forth The knee lifts the knee and lower limb to the bridging position, pausing to tolerate the bridge position and then slowly lowering and then repeating the move                              Third Movement: In supine position, with elbows resting on the ground, lift the servo upward for six seconds and then rest for three seconds. Repeat this motion.                                                                                                Fourth move: Sleeping behind each foot with the help of hands. The abdomen closes and stretches for six seconds, then lifts the opposite leg. Fifth move: The person is placed in a four-legged position, with the elbow flexing upward and downward, and the elbow flexion at least shrinks and the elbow returns to normal.                                                                      Sixth Movement: While lying on his back while knee flexing, his abdomen is contracted into the abdomen, adhering repeatedly to the ground, maintaining the contraction for six seconds, and the movements are repeated. Intervention 2: Control group: Patients with acute low back pain who do not receive exercise.</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:
Patients' information includes family name and confidential registration and access to researcher and related researcher
 But the information extracted and the results of the study will be published in the form of a master's thesis and the resulting papers

When:
Access will usually be available to clients and undergraduates at the University Central Library after completion of the defense and dissertation procedures.
Estimated time is the end of 2019 and the article extracted from it is likely to be available in related journals in 2020

To whom:
Undergraduate Students of Tehran Azad University Central Branch

Conditions:
For use in academic and hospital research

Where to obtain:
Islamic Azad University Central Library Web site

How to obtain:
After registration at Azad University Central Library, applicants can access the full text or abstract of the dissertation and related article if they are a student of Azad University

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Leila rezaei</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 5, Pamcal Alley,etaati strteet,marzdaran town</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1464764319</zip>
        <telephone>+98 21 8823 0532</telephone>
        <email>leila.rezaei.sport@gmail</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Leila rezaei</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 5, Pamcal Alley,etaati street,marzdaran town</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1464764319</zip>
        <telephone>+98 21 8823 0532</telephone>
        <email>Leila.rezaei.sport@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Written and informed consent to the study process
Diagnosis of brucellosis based on history and laboratory examination
Ages 15 to 75 years
Acute low back pain (LBP less than three weeks old)</inclusion_criteria>
      <agemin>15 years</agemin>
      <agemax>75 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>History of surgery in the spinal cord
 Cancer
History of fractures and discopaty in the spine
Infectious disease or renal, pulmonary, cardiac and hepatic diseases
Severe psychiatric illness
Alcohol consumption of psychotropic drugs</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>A23.0</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Brucellosis due to Brucella melitensis</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Stabilization Exercise Group Exercise Program: In this group, the sample will perform training sessions in 42 sessions under the supervision of a sports medicine specialist and physical education expert, in 3 sessions per day for 2 weeks in each session for approximately 10 minutes. At the beginning of each treatment session, a warm-up (about 5 minutes) will consist of light stretching exercises and each exercise will be repeated in 3 sets. The overload and incremental increase of each exercise will be monitored and determined with respect to the correct execution and pressure of the exercise in the previous session. The goal is to maximize the repetitions of each exercise per set. The major emphasis will be on the multifidus and transverse abdominal muscles. All movements should be performed ten times in painless range. Ten minutes in the morning, ten minutes in the afternoon and ten minutes in the evening. Intervention group: Patients with low back pain will undergo core stability training called core stability training. 2 to 3 times and 10 times each. Repeat the first move: the person pulls the legs up and down in a cramped position while the legs are rotating. The second move: back and forth The knee lifts the knee and lower limb to the bridging position, pausing to tolerate the bridge position and then slowly lowering and then repeating the move                              Third Movement: In supine position, with elbows resting on the ground, lift the servo upward for six seconds and then rest for three seconds. Repeat this motion.                                                                                                Fourth move: Sleeping behind each foot with the help of hands. The abdomen closes and stretches for six seconds, then lifts the opposite leg. Fifth move: The person is placed in a four-legged position, with the elbow flexing upward and downward, and the elbow flexion at least shrinks and the elbow returns to normal.                                                                      Sixth Movement: While lying on his back while knee flexing, his abdomen is contracted into the abdomen, adhering repeatedly to the ground, maintaining the contraction for six seconds, and the movements are repeated.</i_keyword>
      <i_keyword>Control group: Patients with acute low back pain who do not receive exercise</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The amount of pain. Timepoint: Measurement of pain at baseline and after 2 weeks of treatment. Method of measurement: Pain Questionnaire(Visual Analogue Score).</prim_outcome>
      <prim_outcome>Lumbar muscles endurance. Timepoint: Measurement of lumbar muscle endurance at baseline and 2 weeks after treatment initiation. Method of measurement: The number of lumbar muscle contractions based on the Sorensen test.</prim_outcome>
      <prim_outcome>َََُAbdominal muscles endurance. Timepoint: Abdominal muscle endurance measurement at baseline and 2 weeks after initiation of treatment. Method of measurement: Sit up test(crunch test).</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>Islamic Azad University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-07-06</approval_date>
        <contact_name>Ethics committee of Zanjan University of Medical Sciences</contact_name>
        <contact_address>Azadi blvd.zanjan zanjan Zanjan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
