<?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>IRCT2015090723937N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2016-10-15</date_registration>
      <primary_sponsor>Vice chancellor for research,Shahid Beheshti University of Medical Sciences Faculity Of Nursing And</primary_sponsor>
      <public_title>The effect of an educational intervention regarding the warning signs of cancer in knowledge and perceived beliefs of women who are coming to the health centers related to the Bushehr University of Medical Sciences by applying the Health Belief Model, 2014-2015</public_title>
      <acronym></acronym>
      <scientific_title>The effect of an educational intervention regarding the warning signs of cancer in knowledge and perceived beliefs of women who are coming to the health centers related to the Bushehr University of Medical Sciences by applying the Health Belief Model, 2014-2015</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2015-09-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>160</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/20324</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention.</study_design>
      <phase>2-3</phase>
      <hc_freetext>Condition 1: Health Belief Model. Condition 2: knowledge. Condition 3: cancer. Condition 4: warning signs of cancer.</hc_freetext>
      <i_freetext>Intervention 1: Cases: In this study, after obtaining permission first 11 urban health center affiliated city health center were classified in four clusters (Each cluster consists of three centers of the North, East, West and also the center of a cluster depend on the outskirts of the city of Bushehr found). Then randomly selected from each of the clusters was a center (Two to be selected for the intervention group and two samples of the control). Samples were selected in the centers, according to inclusion criteria were randomly.During the first session, a pre-test questionnaires containing demographic information - health and perceived knowledge and beliefs (questions based model structures) by the women in the study in two groups of four health center completed. After running pre test according to information obtained from the analysis of questionnaires, review of educational intervention program was designed. Then, for the women in the intervention group training sessions with lectures, Q &amp; A, group discussion and small group discussion in two of the samples performed in coordination with the authorities and centers (5 training sessions of 30-45 minutes). Sessions once a week over a period of five weeks are held in centers.After the post-test at the end of training sessions, the questionnaire was completed by a group intervention. Intervention 2: Control group: firstly to all participants in the control group and the intervention group was completed questionnaires were distributed and only by them (without any training). Finally, after the final post-test training materials available in the intervention group was the control group.</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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Sharifikia Iman</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery,Intersection Niayesh, Tehran,</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 21 8820 2508</telephone>
        <email>Sharifikia@sums.ac.ir</email>
        <affiliation>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Rohani Camelia</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery, Intersection Niayesh,Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 219122796907</telephone>
        <email>Camelia.rohani@yahoo.com</email>
        <affiliation>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: women referred to health centers of the city are covered by the centers and family health records. The subjects were literate and be able to respond to questions in the questionnaire. Of samples in the study were not diagnosed with cancer;Exclusion criteria: participation in training sessions and absences in more than one session</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>100 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
      <hc_code></hc_code>
      <hc_code>c80.9</hc_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
      <hc_keyword></hc_keyword>
      <hc_keyword>Malignant neoplasm, primary site unspecified      Cancer NOS     Carcinoma NOS     Malignancy NOS     Malignant cachexia NOS     Multiple cancer NOS</hc_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Cases: In this study, after obtaining permission first 11 urban health center affiliated city health center were classified in four clusters (Each cluster consists of three centers of the North, East, West and also the center of a cluster depend on the outskirts of the city of Bushehr found). Then randomly selected from each of the clusters was a center (Two to be selected for the intervention group and two samples of the control). Samples were selected in the centers, according to inclusion criteria were randomly.During the first session, a pre-test questionnaires containing demographic information - health and perceived knowledge and beliefs (questions based model structures) by the women in the study in two groups of four health center completed. After running pre test according to information obtained from the analysis of questionnaires, review of educational intervention program was designed. Then, for the women in the intervention group training sessions with lectures, Q &amp; A, group discussion and small group discussion in two of the samples performed in coordination with the authorities and centers (5 training sessions of 30-45 minutes). Sessions once a week over a period of five weeks are held in centers.After the post-test at the end of training sessions, the questionnaire was completed by a group intervention.</i_keyword>
      <i_keyword>Control group: firstly to all participants in the control group and the intervention group was completed questionnaires were distributed and only by them (without any training). Finally, after the final post-test training materials available in the intervention group was the control group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Perceived barriers. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Awareness of the warning signs of cancer. Timepoint: Before and one month after intervention. Method of measurement: Questionnaire awareness.</prim_outcome>
      <prim_outcome>Perceived susceptibility. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Perceived severity. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Perceived benefits. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Guide to action. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Efficacy. Timepoint: Before and one month after intervention. Method of measurement: Structure of Health Belief Questionnaire.</prim_outcome>
      <prim_outcome>Age. Timepoint: Baseline. Method of measurement: Demographic questionnaire.</prim_outcome>
      <prim_outcome>Level of Education. Timepoint: Baseline. Method of measurement: Demographic questionnaire.</prim_outcome>
      <prim_outcome>Previous data from cancer. Timepoint: Before and one month after intervention. Method of measurement: questionnaire.</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>Vice chancellor for research,Shahid Beheshti University of Medical Sciences Faculity Of Nursing And</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2015-07-20</approval_date>
        <contact_name>Bushehr University of Medical Sciences Ethics Committee</contact_name>
        <contact_address>Salman Farsi street, Bahmani Bushehr  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2015-12-14</approval_date>
        <contact_name>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery Ethics Committee</contact_name>
        <contact_address>Shahid Beheshti University of Medical Sciences Faculity Of Nursing And Midwifery,Intersection Niayesh, Tehran Tehran  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
