<?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>IRCT20171230038142N4</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-12-19</date_registration>
      <primary_sponsor>Esfahan University of Medical Sciences</primary_sponsor>
      <public_title>The effect of corrective exercise training and ergonomics education on service forces with low back pain</public_title>
      <acronym></acronym>
      <scientific_title>Compare the effect of corrective exercise training and ergonomics education on service forces and care aids with low back pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-12-06</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>75</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/35941</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: Assistants and Service Providers will be selected by easy and accessible sampling method according to the entry and exit criteria, so that sample size reaches 75, then using computer encoding into groups of 25, including receiving group Corrective exercises, the group receiving the ergonomic interventions and the control group will be divided, Blinding description: Information will be available to the data analyst after naming and naming.</study_design>
      <phase>2-3</phase>
      <hc_freetext>low back pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: corrective exercise training will be received in this group for 8 weeks, weekly 3 sessions and 40-60 minutes each session. Each training session includes 5 to 10 minutes of general warm-up, 20 to 40 minutes of specialized training (tensile and reinforcement training) and 5-10 minutes of cooing. The exact details of the exercise program are presented in a pamphlet (localized based on the work environment) and will be delivered to any assistance and service personnel and will face face-to-face delivery. Intervention 2: Intervention group: Ergonomics education that will receive their interventions for 8 weeks based on the health and safety regulations of the Ministry of Labor on the state of the body and body movements. By avoiding unnecessary or excessive stresses on the muscles, joints, ligaments, respiratory system and cardiovascular system. In this group, detailed details of the ergonomic intervention will be presented in a pamphlet (localized based on the work environment) and will be delivered to any assistance and service personnel and will face face-to-face delivery. Intervention 3: Control group: this group will not receive special intervention.</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:
All information can be given to the applicants after being unidentifiable and can be dismissed by the research deputy of Isfahan University of Medical Sciences.

When:
Information is available two years after the publication of the results.

To whom:
Researchers in Rehabilitation Sciences, Physical Medicine and Social Medicine can benefit from the results of this study.

Conditions:
In case of using similar supportive and therapeutic methods in patients with low back pain and comparing with current methods.

Where to obtain:
After sending an email to Ar.Safaeian@med.mui.ac.ir and obtaining permission from the research deputy of the Isfahan University of Medical Sciences, information is available.

How to obtain:
Send an email to Ar.Safaeian@med.mui.ac.ir and get permission from the Vice-Chancellor of Research in Isfahan University of Medical Sciences

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Alireza Safaeian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, HezarJereyb St.</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>81746-73461</zip>
        <telephone>+98 31 3668 0048</telephone>
        <email>Ar.Safaeian@med.mui.ac.ir</email>
        <affiliation>Esfahan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Alireza Safaeian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Isfahan University of Medical Sciences, Hezar Jereb Street.</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>81746-73461</zip>
        <telephone>+98 31 3668 0048</telephone>
        <email>Ar.Safaeian@med.mui.ac.ir</email>
        <affiliation>Esfahan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Employment in Al-Zahra, Kashani and Khorshid Hospitals in Isfahan
Have at least reading and writing skills
Having a back pain in more than three months
Present written consent for participation in the research</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>60 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Specific low back pain such as infection, rheumatoid diseases, congenital anomalies, history of cancer according to history and health
Having a history of vertebral surgery, spinal tumor, history of spinal fracture and multiple sclerosis
Having a health ban to do sports exercises</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M54.5</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Low back pain</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: corrective exercise training will be received in this group for 8 weeks, weekly 3 sessions and 40-60 minutes each session. Each training session includes 5 to 10 minutes of general warm-up, 20 to 40 minutes of specialized training (tensile and reinforcement training) and 5-10 minutes of cooing. The exact details of the exercise program are presented in a pamphlet (localized based on the work environment) and will be delivered to any assistance and service personnel and will face face-to-face delivery.</i_keyword>
      <i_keyword>Intervention group: Ergonomics education that will receive their interventions for 8 weeks based on the health and safety regulations of the Ministry of Labor on the state of the body and body movements. By avoiding unnecessary or excessive stresses on the muscles, joints, ligaments, respiratory system and cardiovascular system. In this group, detailed details of the ergonomic intervention will be presented in a pamphlet (localized based on the work environment) and will be delivered to any assistance and service personnel and will face face-to-face delivery.</i_keyword>
      <i_keyword>Control group: this group will not receive special intervention.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Compare the effect of corrective exercise training and ergonomics education on service forces and care aids with low back pain Using the Visual Analogue Scale (VAS). Timepoint: Before and after intervention and eight weeks after the end of intervention, in each of the three groups, the pain intensity was measured using VAS pain scale. Method of measurement: Using a 10-point VAS pain scale, this scale indicates zero pain and the number 10 indicates a high pain.</prim_outcome>
      <prim_outcome>The Effect of Rehabilitation Exercise Training and Training on the Principles of Ergonomics in Helping Surveyors and Service Persons with Back Pain by Using the Ossourist Disability Questionnaire. Timepoint: Before the intervention and eight weeks after the intervention, all of the three groups will be asked about the disability by using the osoestory disability inventory questionnaire. Method of measurement: The Osustory Disability Questionnaire was questioned and evaluated in 10 sections (each section containing 6 questions) including pain intensity, personal work, lifting, walking, sitting, standing, sleeping, sexual activity, social life, and travel. Gives.</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>Esfahan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-12-02</approval_date>
        <contact_name>Isfahan University of Medical Sciences</contact_name>
        <contact_address>Isfahan University of Medical Sciences, HezarJereyb St. Isfahan Isfehan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
