<?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>IRCT20250530065982N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-07-06</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>The effect of educational programs on reproductive preferences and childbearing motivations</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the Impact of an Educational Program Based on the Transtheoretical Model on Fertility Preferences and Childbearing Motivations Among Married Students</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-07-12</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/84296</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Participants were randomly assigned to either the intervention or control group. Each group consisted of 30 participants, and block randomization was employed for allocation. The blocking scheme included the following six permutations: CTTC, CTCT, CCTT, TCCT, TCTC, and TTCC, where "T" denotes the intervention group and "C" represents the control group. To generate the allocation sequence, random numbers between 0 and 6 were produced using the RANDBETWEEN function in Microsoft Excel. Based on the generated number, one of the predefined blocks was selected, and participants were allocated accordingly. This randomization method ensured equitable and systematic distribution of participants between the two groups, minimizing selection bias and enhancing the validity of the study.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Educational program based on a meta-theoretical model on reproductive preferences and childbearing motivations in married students.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: The intervention group participated in a 7-session educational program (1-2 hours per session) grounded in the Transtheoretical Model, designed to modify fertility preferences, enhance childbearing motivations, and promote self-care behaviors. Immediately following the intervention, both groups completed standardized questionnaires assessing fertility preferences and childbearing motivations. Follow-up evaluations were conducted at 1-month and 3-month intervals post-intervention to examine sustained effects. Participants requiring additional support received individualized counseling sessions, delivered either in-person or via telephone. Throughout the study period, the control group received only standard institutional education while undergoing identical assessment procedures at matching timepoints. This rigorous methodology ensured systematic evaluation of the intervention's effectiveness while maintaining ethical standards of participant care. Intervention 2: Control group: This group didn't receive any new training and only received routine university training and classes.</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 study data will be made shareable after complete de-identification of participants.

When:
The access period begins 6 months after the results are published.

To whom:
Researchers

Conditions:
By citing a logical reason, citing the source, and conducting analyses.

Where to obtain:
Researchers may request the data by contacting Dr. Mahsa Al-Sadat Mousavi via email: mousavi1315@gmail.com

How to obtain:
Following a 6-month post-publication period, data may be obtained by submitting a formal request with valid justification to the corresponding author, Dr. Mahsa Al-Sadat Mousavi. Approved requests will be fulfilled within 10 business days.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Hedieh Kamrava</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Islamic Azad University, Isfahan (Khorasgan) Branch, Daneshgah boulevard, Arqavanieh, East Jey street, Isfahan</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>81551-39998</zip>
        <telephone>+98 31 3500 2000</telephone>
        <email>Hediehkamrava1377@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Mahsa sadat Mousavi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Islamic Azad University, Isfahan (Khorasgan) Branch, Daneshgah boulevard, Arqavanieh, East Jey street, Isfahan</address>
        <city>Isfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>81551-39998</zip>
        <telephone>+98 31 3500 2000</telephone>
        <email>mousavi1315@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Willingness to participate in the study
Literacy (ability to read and write)
Being married
Living with one's spouse
Age range: 18–35 years
Using a contraceptive method
No current or immediate future pregnancy planning</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>35 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Diagnosis of a chronic illness
Any medical contraindication for childbearing</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>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: The intervention group participated in a 7-session educational program (1-2 hours per session) grounded in the Transtheoretical Model, designed to modify fertility preferences, enhance childbearing motivations, and promote self-care behaviors. Immediately following the intervention, both groups completed standardized questionnaires assessing fertility preferences and childbearing motivations. Follow-up evaluations were conducted at 1-month and 3-month intervals post-intervention to examine sustained effects. Participants requiring additional support received individualized counseling sessions, delivered either in-person or via telephone. Throughout the study period, the control group received only standard institutional education while undergoing identical assessment procedures at matching timepoints. This rigorous methodology ensured systematic evaluation of the intervention's effectiveness while maintaining ethical standards of participant care.</i_keyword>
      <i_keyword>Control group: This group didn't receive any new training and only received routine university training and classes.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Individuals' desire and planning to have children. Timepoint: Before the start of the intervention, immediately after the intervention, 1 month after the start of the intervention, 3 months after the start of the intervention. Method of measurement: Childbearing Motivation Questionnaire.</prim_outcome>
      <prim_outcome>The score each participant receives from the Fertility Preferences Questionnaire. Timepoint: Before the start of the intervention, immediately after the intervention, 1 month after the start of the intervention, 3 months after the start of the intervention. Method of measurement: Reproductive Preferences 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>Islamic Azad University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-03-13</approval_date>
        <contact_name>Research Ethics Committees of Islamic Azad University-Yazd Branch</contact_name>
        <contact_address>Shohadaye Gomnam boulevard, Safaieh, Yazd Yazd Yazd Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
