<?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>IRCT20251206068227N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-08-03</date_registration>
      <primary_sponsor>Yazd University of Medical Sciences</primary_sponsor>
      <public_title>Investigating the effect of counseling based on the sexual health model on the Sexual compatibility and Intention to have children of newly married women</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the effect of counseling based on the sexual health model on the Sexual compatibility and Intention to have children of newly married women</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-03-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>64</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/89145</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Other design features: We have two intervention and control groups. The intervention group (32 people will be trained in the first session in the form of in-person educational classes and the remaining sessions will be in-person or virtual online via Sky Room, depending on the preference of the people) and 32 people will be placed in the active control group (32 people will receive a virtual training package), Randomization description: the sample size is 64 .after the number of qualified people has reached 64 , the random allocation of block is done using the online allocation online site ( http://www.randomization.com ) and 32 people in the intervention group ( 32 members of the first session under training in the form of educational presence classes ) and the rest of the sessions will be placed online via sky and 32 people in active control group ( 32 people ) .participants are informed that the probability of their placement in each group of control and intervention groups is 50 % .the random allocation process consists of two stages : 1 ) generating a pre - nasal random assignment , using a computer random number table .the table of random numbers is used to use the online method in online software .2 ) concealment : the implementation of the sequence in a way that masks the interventions until the participants are formally assigned to their groups ( by one of the health care providers outside the research team ) .</study_design>
      <phase>N/A</phase>
      <hc_freetext>Condition 1: sexual compatibility. Condition 2: Intention to have children.</hc_freetext>
      <i_freetext>Intervention group: the intervention group received counseling and question and response therapy sessions during 4 sessions of 90 - minute sessions of counseling that will be received in the first session of counseling in the form of educational presence classes and the rest of sessions , depending on the willingness of individuals under training or virtual consulting . education is based on sexual health model and focusing on sexual adaptation in groups 6 - 8 ..</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 data, including proposals, raw data, and project reports

When:
Data is accessible via request from the legal system for two years, 6 months after publication.

To whom:
All natural and legal persons will have access upon request to the Vice President for Research of Yazd University of Medical Sciences.

Conditions:
For legal matters and the need to use data in future studies

Where to obtain:
Fatemeh Pourhakkak, Mahshid Bokaei

How to obtain:
After submitting the application to the Yazd Medical Sciences Research and Technology Vice-Chancellor, a call will be issued to the executor to provide data.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>fatemeh poorhakkak</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Chamran Street, 17th Shahrivar Street</address>
        <city>yazd</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8914687795</zip>
        <telephone>36245975</telephone>
        <email>F.poorhakkak242@gmail.com</email>
        <affiliation>Yazd University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mahshid Bekai</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Bu Ali Street, Faculty of Nursing and Midwifery</address>
        <city>Yazd</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7744389168</zip>
        <telephone>+98 35 3824 1751</telephone>
        <email>mah_bokaie@yahoo.com</email>
        <affiliation>Yazd University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Being Iranian and literate
Being monogamous
Having regular sexual activity (at least once a week)
Having weak to moderate sexual compatibility based on the Hurlburt Sexual Compatibility Questionnaire (score less than 64)
A maximum of one year has passed since the marriage
Having access to a smartphone and the internet 7. Permanent marriage
Permanent marriage</inclusion_criteria>
      <agemin>15 years</agemin>
      <agemax>45 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Previous marital history for both partners
Experience of a severe problem or stressful event (such as the death of a loved one or financial bankruptcy) in the past 6 months for both partners (self-reported)
Having a physical illness (including no sexual dysfunction, sexually transmitted diseases, and medical illnesses such as diabetes) or a major mental illness based on the couples' self-report
History of treatment for sexual dysfunction by a psychologist, urologist, or gynecologist
Participation in similar sexual counseling courses in the year before the study (both groups received only premarital sexual counseling)
Presence of acute marital conflict (including lawsuits, infidelity)
History of use of drugs, alcohol, and sexual enhancement drugs or drugs that affect sexual function
Presence of a known abnormality in sexual anatomy and function
Pregnancy (self-reported)
Forced marriage</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: the intervention group received counseling and question and response therapy sessions during 4 sessions of 90 - minute sessions of counseling that will be received in the first session of counseling in the form of educational presence classes and the rest of sessions , depending on the willingness of individuals under training or virtual consulting . education is based on sexual health model and focusing on sexual adaptation in groups 6 - 8 .</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Sexual compatibility score in Hurlbert sexual compatibility questionnaire. Timepoint: before intervention and 4 and 8 weeks after intervention. Method of measurement: Hurlbert sexual compatibility questionnaire.</prim_outcome>
      <prim_outcome>The mean of childbearing intention in the questionnaire of childbearing intention. Timepoint: before intervention and 4 and 8 weeks after intervention. Method of measurement: questionnaire of effective component on childbearing intention.</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>Yazd University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-11-05</approval_date>
        <contact_name>Ethics Committee of Yazd University of Medical Sciences</contact_name>
        <contact_address>Yazd, Safaiyeh, Bu Ali St., opposite the Infertility Center yazd Yazd Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
