<?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>IRCT20150128020854N9</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-03-22</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>The comparison of the effectiveness of narrative therapy and the “Good- Enough Sex Model" on sexual attitude, sexual function, and sexual satisfaction.</public_title>
      <acronym></acronym>
      <scientific_title>The comparison of the effectiveness of narrative therapy and “Good- Enough Sex Model" on sexual attitude, sexual function, and sexual satisfaction in infertile married persons.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-04-19</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>48</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/54870</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: From infertile married men and women referring to a specialized urology and gynecology office in Tehran city, 48 persons will be selected according to the research criteria and then will be assigned randomly to 3 groups of 16. At First, the participants will be given two-digit codes from 01 to 48. Then, using the website www.Randomization.com, three sets of codes will be selected, the first set will be assigned as the intervention group with narrative therapy, the second as the intervention group with  “Good- Enough Sex Model",  and third as the control group.</study_design>
      <phase>N/A</phase>
      <hc_freetext>sexual counselling.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group "Narrative therapy": After completing the written consent form, Dehghani Sexual Attitude Questionnaire along with Rosen Sexual Function Questionnaire and Hudson Sexual Satisfaction Questionnaire will be completed as a pre-test by 16 samples of this group. This intervention is performed in 3 stages in 4 sessions of 60 minutes at one week intervals. The first stage: the narrative stage of the problem, which is done by aiming at another form of the problem as an incidence (externalization) by focusing on their effects instead of their causes. The second stage: the stage of finding exceptions with the purpose Discoveries of relative victories are made over problems and examples of effective measures. Stage Three: Attracting support, encouraging some form of public behavior for newer and preferred interpretations, transforms past private cognitive structures into socially supported actions. Carefully tuned questions are used to achieve operational goals related to the three steps. This series of questions includes: deconstruction questions, space opener questions, preferential questions, questions to present the story, semantic questions and questions to lead the story to the future. 45 days after the intervention, the questionnaires are completed again by the samples and will be compared with the pre-test results. Intervention 2: Intervention group "Good-enough sex mode": After completing the written consent form, Dehghani Sexual Attitude Questionnaire along with Rosen Sexual Function Questionnaire (FSFI and IIEF) and Hudson Sexual Satisfaction Questionnaire (ISS) will be completed as a pre-test by 16 samples of this group. The "Sexually Enough Good enough" model is implemented in 4 sessions with the following objectives: In the first session, the two goals of meaning and place of sexual experience in everyday life (fusion of sexual experience with real life) are examined and the relationship between Realistic sexual expectations are followed by behavioral, physical health and sexual satisfaction. In the second session, the two objectives are the relationship between the quality of sexual experience and optimal performance (questioning perfect and perfect performance) and the relationship between enrichment in dimension. Intimate and sexual satisfaction is pursued. The third session is followed with the aim of assigning meaning, goals and tasks to each couple to achieve sexual satisfaction. The fourth session aims to point out and focus on all psychological, medical and communication aspects to promote health Sex is followed. 45 days after the intervention, the questionnaires are completed again by the samples and will be compared with the pre-test results. Intervention 3: Control group: After completing the written consent form, the Dehghani Sexual Attitude Questionnaire along with the Rosen Sexual Function Questionnaire (FSFI and IIEF) and the Hudson Sexual Satisfaction Questionnaire (ISS) will be completed as a pre-test by 16 samples of this group. Information and educational intervention in the field of attitude, practice and sexual satisfaction 45 days after the intervention in the intervention groups, the questionnaires will be completed again by the control group and the results will be compared with the pre-test scores.</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>No - There is not a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for not sharing IPD is Because the results will be mentioned in the article.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Armin Firoozi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Psychology and Social Science, Roodehen Branch, Islamic Azad University,  University Complex, Ayatollah Khamenei Blvd, Roodehen,</address>
        <city>Roodhen</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3973188981</zip>
        <telephone>+98 21 7650 5015</telephone>
        <email>info@riau.ac.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Hedyeh Riazi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Valiasr</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985717443</zip>
        <telephone>+98 21 2088 1225</telephone>
        <email>h.riazi@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>Inclusion criteria: Literacy, 
diagnosis of infertility by a gynecologist and urologist, 
age between 20 to 45 years, 
no severe marital conflict, 
having at least one sexual intercourse per week, 
2 to 4 years after infertility diagnosis, 
no participation in psychological interventions in the last 6 months, 
have primary infertility of female or male origin, 
have experience in infertility treatment (any method), 
informed consent of couples to participate in treatment sessions</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>45 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>having a neurological and systemic disease based on a medical record, 
having a urinary-genital infection based on a medical record, 
having a severe mental disorder (psychosis disorder) and taking psychiatric drugs based on a medical record, 
mental retardation, 
using alcohol, drugs and medication,</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Z70.3</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Counseling related to combined concerns regarding sexual attitude, behavior and orientation</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group "Narrative therapy": After completing the written consent form, Dehghani Sexual Attitude Questionnaire along with Rosen Sexual Function Questionnaire and Hudson Sexual Satisfaction Questionnaire will be completed as a pre-test by 16 samples of this group. This intervention is performed in 3 stages in 4 sessions of 60 minutes at one week intervals. The first stage: the narrative stage of the problem, which is done by aiming at another form of the problem as an incidence (externalization) by focusing on their effects instead of their causes. The second stage: the stage of finding exceptions with the purpose Discoveries of relative victories are made over problems and examples of effective measures. Stage Three: Attracting support, encouraging some form of public behavior for newer and preferred interpretations, transforms past private cognitive structures into socially supported actions. Carefully tuned questions are used to achieve operational goals related to the three steps. This series of questions includes: deconstruction questions, space opener questions, preferential questions, questions to present the story, semantic questions and questions to lead the story to the future. 45 days after the intervention, the questionnaires are completed again by the samples and will be compared with the pre-test results.</i_keyword>
      <i_keyword>Intervention group "Good-enough sex mode": After completing the written consent form, Dehghani Sexual Attitude Questionnaire along with Rosen Sexual Function Questionnaire (FSFI and IIEF) and Hudson Sexual Satisfaction Questionnaire (ISS) will be completed as a pre-test by 16 samples of this group. The "Sexually Enough Good enough" model is implemented in 4 sessions with the following objectives: In the first session, the two goals of meaning and place of sexual experience in everyday life (fusion of sexual experience with real life) are examined and the relationship between Realistic sexual expectations are followed by behavioral, physical health and sexual satisfaction. In the second session, the two objectives are the relationship between the quality of sexual experience and optimal performance (questioning perfect and perfect performance) and the relationship between enrichment in dimension. Intimate and sexual satisfaction is pursued. The third session is followed with the aim of assigning meaning, goals and tasks to each couple to achieve sexual satisfaction. The fourth session aims to point out and focus on all psychological, medical and communication aspects to promote health Sex is followed. 45 days after the intervention, the questionnaires are completed again by the samples and will be compared with the pre-test results.</i_keyword>
      <i_keyword>Control group: After completing the written consent form, the Dehghani Sexual Attitude Questionnaire along with the Rosen Sexual Function Questionnaire (FSFI and IIEF) and the Hudson Sexual Satisfaction Questionnaire (ISS) will be completed as a pre-test by 16 samples of this group. Information and educational intervention in the field of attitude, practice and sexual satisfaction 45 days after the intervention in the intervention groups, the questionnaires will be completed again by the control group and the results will be compared with the pre-test scores.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Sexual attitude. Timepoint: Before the intervention, one week and 45 days after the intervention. Method of measurement: Sexual Attitudes Questionnaire.</prim_outcome>
      <prim_outcome>Sexual function. Timepoint: Before the intervention, one week and 45 days after the intervention. Method of measurement: Sexual Function Questionnaire.</prim_outcome>
      <prim_outcome>Sexual satisfaction. Timepoint: Before the intervention, one week and 45 days after the intervention. Method of measurement: Sexual Satisfaction 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>2021-02-21</approval_date>
        <contact_name>Ethics Committee of Islamic Azad University of Medical Sciences, Tehran</contact_name>
        <contact_address>Tehran, Islamic Azad University of Medical Sciences, aculty of Medicine Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
