<?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>IRCT20210301050542N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-03-16</date_registration>
      <primary_sponsor>Trabiat Modares University</primary_sponsor>
      <public_title>Evaluation of the Effect of Educational Intervention on Neck Pain</public_title>
      <acronym></acronym>
      <scientific_title>Designning and Evaluating Educational Intervention Based on  Health Belief Model in  Neck Pain Prevention Behaviors  in Teachers.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-05-10</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>140</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/54696</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Triple blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Other design features: Design of educational intervention based on health belief model, Randomization description: First, the names of all schools will be specified with a code and the relevant codes will be poured into a bag, or the computer will be randomly divided into two groups (test and control) using the computer method. After dividing the schools into two groups of control and test, the names of all teachers are re-identified and a bag is poured into the bag and people will be randomly selected from the bag and divided into two groups. Each group of 70 people will be selected for the study. 70 people will be selected as the control group and 70 people as the experimental group. To prevent any predictions by the participants and the researcher, the random allocation concealment method will be used, Blinding description: In this research, the researcher, the participants in the research and the people analyzing the data do not know the names of the people. The participants in the research will be identified based on the code and no personal information will be collected from the people in the research.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Neck Pain.</hc_freetext>
      <i_freetext>Intervention 1: "Intervention group:" This group is trained for one month in a virtual way by holding webinars, presenting educational clips, pamphlets and posters, after which they will be under reminder trainings for 2 months. Intervention 2: "Control group:"  There are 70 junior high school teachers who will not receive any intervention during the research period. Before the intervention, immediately after the intervention, and three months after the intervention, they will fill in the researcher-made questionnaire and the results It will be compared with the results of the intervention group and statistical analysis.</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:
Part of the data related to the main consequences can be shared.

When:
Six months after the results were published

To whom:
The data will be available only to researchers working in academic and scientific institutions.

Conditions:
Repeated measurement analysis to evaluate the effect of training duration six months after the last intervention.

Where to obtain:
By sending an email to the email address zohremoradi@modares.ac.ir

How to obtain:
One week after sending the email, the applicant will respond to the email address zohremoradi@modares.ac.ir.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Sedigheh Sadat Tavafian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Tarbiat Modares University, Nasr Bridge, Jala Al-Ahmad Highway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1411713116</zip>
        <telephone>+98 21 8288 4547</telephone>
        <email>tavafian@modares.ac.ir</email>
        <affiliation>Tarbiat Modares University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Sedigheh Sadat Tavafian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Tarbiat Modares University, Nasr Bridge, Jala Al-Ahmad Highway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1411713116</zip>
        <telephone>+98 21 8288 4547</telephone>
        <email>tavafian@modares.ac.ir</email>
        <affiliation>Tarbiat Modares University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Teachers who have access to the internet, mobile phones and the skills to use them.</inclusion_criteria>
      <agemin>25 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>People's unwillingness to continue participating in research.
Teachers who have a second job.
People with congenital musculoskeletal disorders of the neck.
People with a history of surgery, neck fractures and significant neck pain.
People who have a doctor forbidding them to do sports.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M54.02</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Panniculitis affecting regions of neck and back, cervical region</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>N/A</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>"Intervention group:" This group is trained for one month in a virtual way by holding webinars, presenting educational clips, pamphlets and posters, after which they will be under reminder trainings for 2 months.</i_keyword>
      <i_keyword>"Control group:"  There are 70 junior high school teachers who will not receive any intervention during the research period. Before the intervention, immediately after the intervention, and three months after the intervention, they will fill in the researcher-made questionnaire and the results It will be compared with the results of the intervention group and statistical analysis.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Awareness. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Perceived sensitivity. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Severely perceived. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Perceived benefits. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Perceived obstacles. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Cues to Action. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Efficacy. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
      <prim_outcome>Behavior. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Neck pain prevention behavior score. Timepoint: Before the intervention and immediately after the intervention, three months after the intervention. Method of measurement: Researcher-made questionnaire.</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>Trabiat Modares University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-01-13</approval_date>
        <contact_name>Ethics Committee of Tarbiat Modares University</contact_name>
        <contact_address>Tarbiat Modares University, Nasr Bridge,  Jalal Al-Ahmad Highway Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
