<?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>IRCT20220829055818N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2023-07-01</date_registration>
      <primary_sponsor>Shahid Beheshti University of Medical Sciences</primary_sponsor>
      <public_title>The effect of an educational intervention based on the theory of planned behavior on childbearing intentions in female students of Shahid Beheshti University of Medical Sciences in 2022</public_title>
      <acronym>Childbearing Intentions</acronym>
      <scientific_title>The effect of an educational intervention based on the theory of planned behavior on childbearing intentions in female students</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-09-27</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>100</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/65539</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Education/Guidance, Randomization description: Two Faculties of Nursing-Midwifery and Pharmacy of Shahid Beheshti Medical Sciences are selected as available, and the allocation of samples will be random block. Sampling is done in each faculty based on the purpose and 100 qualified people are divided into two groups of 50 control and 50 intervention groups. On even days of the week, female students in the intervention group and on odd days of the week, female students in the control group receive the necessary training.</study_design>
      <phase>N/A</phase>
      <hc_freetext>childbearing.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: female students. It will be done on 120 people (60 people in the intervention group) of female students studying from Shahid Beheshti Nursing-Midwifery and Pharmacy Faculties of Medical Sciences using the available sampling method, where the allocation of samples will be in a random block. After receiving the letter of introduction and obtaining permission from the head of the research centers, sampling will begin from two faculties. The characteristics of the research samples include the incoming academic semesters of 2019, 2019, and 2019, and in undergraduate degrees in nursing, midwifery, psychiatry, and operating room, and general doctoral degrees in the field of pharmacy, including unmarried students. After completing the informed and written consent form, the research samples entered the study and they were informed that they could withdraw from the study in case of dissatisfaction and unwillingness to cooperate. The data collection tool includes a demographic information questionnaire and the second part includes the constructs of the theory of planned behavior (awareness, attitude, mental norm, perceived behavior control and behavioral intention) which is pre-test-post-test in the space of 1 week from each Two intervention and control groups are taken. The educational content intended for training the intervention group from the available databases, including instructions and educational packages of the Ministry of Health related to childbearing and population in the form of 4 educational PowerPoints with the topics of "conscious marriage, childbearing and parenting, population and challenges, and abortion" embryo" has been prepared. Training is provided only to the intervention group during 2 sessions of 60 minutes in the form of lectures, group discussions and questions and answers by the researcher. Also, before the start of the second session, the materials related to the previous session are reviewed by the researcher. Intervention 2: Control group: female students. It will be done on 120 people (60 people in the control group) of female students who are studying from the nursing-midwifery and pharmacy faculties of Shahid Beheshti Medical Sciences using available sampling method, and the allocation of samples will be done in a random block. After receiving the letter of introduction and obtaining permission from the head of the research centers, sampling will begin from two faculties. The characteristics of the research samples include the incoming academic semesters of 2019, 2019, and 2019, and in undergraduate degrees in nursing, midwifery, psychiatry, and operating room, and general doctoral degrees in the field of pharmacy, including unmarried students. After completing the informed and written consent form, the research samples entered the study and they were informed that they could withdraw from the study in case of dissatisfaction and unwillingness to cooperate. The data collection tool includes a demographic information questionnaire and the second part includes the constructs of the theory of planned behavior (awareness, attitude, mental norm, perceived behavior control and behavioral intention) which is pre-test-post-test in the space of 1 week from each Two intervention and control groups are taken. The control group did not receive training in this field.</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:
It will be in the form of a questionnaire and giving PowerPoint and teaching it.

When:
2 month

To whom:
Professors and students

Conditions:
During and after training

Where to obtain:
Shahid Beheshti Nursing-Midwifery and Pharmacy Faculties

How to obtain:
Test and pre-test process

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Reyhaneh Pourjam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Niayesh Hiway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985717443</zip>
        <telephone>+98 21 8865 5366</telephone>
        <email>Rpourjam76@sbmu.ac.ir</email>
        <affiliation>Shahid Beheshti University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Reyhaneh Pourjam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Niyayesh Hiway</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985717443</zip>
        <telephone>+98 21 8865 5366</telephone>
        <email>Rpourjam76@sbmu.ac.ir</email>
        <affiliation>Shahid Beheshti University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Informed and written consent to participate in the research
Having Iranian nationality
All female students studying
The minimum age is 20 and the maximum age is 35 years</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>35 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Failure to participate in a training session
Unwillingness to continue cooperation in research
Incomplete answers to questionnaire questions</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: female students. It will be done on 120 people (60 people in the intervention group) of female students studying from Shahid Beheshti Nursing-Midwifery and Pharmacy Faculties of Medical Sciences using the available sampling method, where the allocation of samples will be in a random block. After receiving the letter of introduction and obtaining permission from the head of the research centers, sampling will begin from two faculties. The characteristics of the research samples include the incoming academic semesters of 2019, 2019, and 2019, and in undergraduate degrees in nursing, midwifery, psychiatry, and operating room, and general doctoral degrees in the field of pharmacy, including unmarried students. After completing the informed and written consent form, the research samples entered the study and they were informed that they could withdraw from the study in case of dissatisfaction and unwillingness to cooperate. The data collection tool includes a demographic information questionnaire and the second part includes the constructs of the theory of planned behavior (awareness, attitude, mental norm, perceived behavior control and behavioral intention) which is pre-test-post-test in the space of 1 week from each Two intervention and control groups are taken. The educational content intended for training the intervention group from the available databases, including instructions and educational packages of the Ministry of Health related to childbearing and population in the form of 4 educational PowerPoints with the topics of "conscious marriage, childbearing and parenting, population and challenges, and abortion" embryo" has been prepared. Training is provided only to the intervention group during 2 sessions of 60 minutes in the form of lectures, group discussions and questions and answers by the researcher. Also, before the start of the second session, the materials related to the previous session are reviewed by the researcher.</i_keyword>
      <i_keyword>Control group: female students. It will be done on 120 people (60 people in the control group) of female students who are studying from the nursing-midwifery and pharmacy faculties of Shahid Beheshti Medical Sciences using available sampling method, and the allocation of samples will be done in a random block. After receiving the letter of introduction and obtaining permission from the head of the research centers, sampling will begin from two faculties. The characteristics of the research samples include the incoming academic semesters of 2019, 2019, and 2019, and in undergraduate degrees in nursing, midwifery, psychiatry, and operating room, and general doctoral degrees in the field of pharmacy, including unmarried students. After completing the informed and written consent form, the research samples entered the study and they were informed that they could withdraw from the study in case of dissatisfaction and unwillingness to cooperate. The data collection tool includes a demographic information questionnaire and the second part includes the constructs of the theory of planned behavior (awareness, attitude, mental norm, perceived behavior control and behavioral intention) which is pre-test-post-test in the space of 1 week from each Two intervention and control groups are taken. The control group did not receive training in this field.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Intervention Based on the Theory of Planned Behavior on Childbearing. Timepoint: 2 to 3 Weekes. Method of measurement: Pawer Point Education.</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>Shahid Beheshti of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-09-06</approval_date>
        <contact_name>school of pharmacy and nursing &amp; midwifery- shahid beheshti university of medical sciences</contact_name>
        <contact_address>Velenjak St. , Niayesh Highway Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
