<?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>IRCT2015090123852N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2015-10-30</date_registration>
      <primary_sponsor>Ahvaz Jundishapur University of Medical Sciences</primary_sponsor>
      <public_title>A Comparison of SMS and face to face training impacts on performance health screening tests in middle-aged women in Ahvaz</public_title>
      <acronym></acronym>
      <scientific_title>A Comparative study of SMS and face to face training impacts on performance health screening tests in middle-aged women in Ahvaz, Iran</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2015-11-01</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>90</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/20280</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Screening.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Condition 1: doing gynecologic examinations in middle-aged women. Condition 2: doing Pap smear in middle-aged women. Condition 3: doing blood glucose testing in middle-aged women. Condition 4: doing hematocrit testing in middle-aged women. Condition 5: doing tests of hemoglobin in middle-aged women. Condition 6: doing testing, lipid profiles in middle-aged women.</hc_freetext>
      <i_freetext>Intervention 1: control group: The control group will receive a face to face training for 4 sessions held fortnight in two months in a healthcare centers. The content of the meetings and is based on the educational needs of individuals and a lecture is presented by the investigator. Each session lasts 45 minutes. The questions will be finally answered and a pamphlet of the contents discussed in the educational sessions will be available to people. Intervention 2: The intervention group: A Same educational content in a form of short messages (or SMS) is provided for the experimental group. The researcher will send SMS every other day for two months from 8 am to 8 pm. The sentences are sent regularly. In the first day a message is sent in a form of question or news for the sake of their mental preparation and then its answer is sent in the next SMS, so people will be prepared for the next SMS. The participants are allowed to provide their feedback regarding the screening tests within a month as soon as the study completes. During this period the researcher calls the experimental group every fortnight and answers their questions. Both groups are then asked about the screening tests. Time and visit confirmation of people are checked using the documents at healthcare centers.</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>Shahnaz Najar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 90, Western ten, Kianpars, Ahvaz</address>
        <city>Ahvaz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 61 3373 8482</telephone>
        <email>Najarshanaz@yahoo.com</email>
        <affiliation>Ahvaz Jundishapur University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Elham alihossaini</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Ahvaz Jundishapur University of Medical Sciences, Golestan Blvd, Ahvaz</address>
        <city>Ahvaz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 61300000000</telephone>
        <email>alihossaini.e@ajums.ac.ir, e.alihossaini@gmail.com</email>
        <affiliation>Ahvaz Jundishapur 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>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: Forty to sixty year old women; having a mobile phone phone; and the eligibility for gynecologic exams, Pap smears, blood biochemical tests (lipid profile, blood glucose, hemoglobin, hematocrit). Exclusion criteria: Suffering from a mental disease; suffering from a any chronic disease such as diabetes, hypertension, etc;  does not participate in 2 training sessions.</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>60 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Z01.4</hc_code>
      <hc_code>Z01.4</hc_code>
      <hc_code>Z01.7</hc_code>
      <hc_code>Z01.7</hc_code>
      <hc_code>Z01.7</hc_code>
      <hc_code>Z01.7</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Pelvic examination (annual)(periodic)</hc_keyword>
      <hc_keyword>Papanicolaou smear of cervix</hc_keyword>
      <hc_keyword>Laboratory examination</hc_keyword>
      <hc_keyword>Laboratory examination</hc_keyword>
      <hc_keyword>Laboratory examination</hc_keyword>
      <hc_keyword>Laboratory examination</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Early detection</i_code>
      <i_code>Early detection</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>control group: The control group will receive a face to face training for 4 sessions held fortnight in two months in a healthcare centers. The content of the meetings and is based on the educational needs of individuals and a lecture is presented by the investigator. Each session lasts 45 minutes. The questions will be finally answered and a pamphlet of the contents discussed in the educational sessions will be available to people.</i_keyword>
      <i_keyword>The intervention group: A Same educational content in a form of short messages (or SMS) is provided for the experimental group. The researcher will send SMS every other day for two months from 8 am to 8 pm. The sentences are sent regularly. In the first day a message is sent in a form of question or news for the sake of their mental preparation and then its answer is sent in the next SMS, so people will be prepared for the next SMS. The participants are allowed to provide their feedback regarding the screening tests within a month as soon as the study completes. During this period the researcher calls the experimental group every fortnight and answers their questions. Both groups are then asked about the screening tests. Time and visit confirmation of people are checked using the documents at healthcare centers.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Doing Pap smear. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</prim_outcome>
      <prim_outcome>Doing gynecologic examinations. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</prim_outcome>
      <prim_outcome>Doing tests, lipid profiles. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</prim_outcome>
      <prim_outcome>Doing testing blood sugar. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</prim_outcome>
      <prim_outcome>Doing hematocrit blood test. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</prim_outcome>
      <prim_outcome>Doing tests of hemoglobin. Timepoint: Before the intervention- one month after the intervention. Method of measurement: Documentation files.</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>Ahvaz Jundishapur University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2015-07-25</approval_date>
        <contact_name>Ahvaz Jundishapur University of Medical Sciences</contact_name>
        <contact_address>Ahvaz Golestan Blvd،Ahvaz Jundishapur University of Medical Sciences Ahvaz  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
