<?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>IRCT20250813066844N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-09-04</date_registration>
      <primary_sponsor>Shahrud County Education Department</primary_sponsor>
      <public_title>Development and Evaluation of an Emotional Intelligence Training Protocol and Comparison with Intensive Short-Term Dynamic Psychotherapy on Experiential Avoidance, Psychological Flexibility, and Psychosomatic Symptoms in Elementary School Teachers</public_title>
      <acronym></acronym>
      <scientific_title>Development and Evaluation of an Emotional Intelligence Training Protocol and Comparison with Intensive Short-Term Dynamic Psychotherapy on Experiential Avoidance, Psychological Flexibility, and Psychosomatic Symptoms in Elementary School Teachers</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-09-12</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/85910</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Individuals are randomly assigned using a random number table to one of two study groups: the experimental group or the control group, and they receive the intervention corresponding to that group, Blinding description: In this study, a (single-blind design) was used. This means that participants were unaware of their assignment to either the experimental or control group. To implement this approach, participants were only informed that they were taking part in a training program aimed at improving psychological skills. However, the specific details regarding the type of intervention and the differences between the groups were not disclosed to them. Thus, participants were not aware of the precise nature of the intervention and did not know whether they were in the experimental or control group. This measure was taken to reduce potential biases resulting from participants' awareness of their group allocation and to enhance the study's internal validity.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Experiential Avoidance, Psychological Flexibility, and Psychosomatic Symptoms.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group:  After random assignment, participants receive 10 weekly sessions of 90-minute emotional intelligence training based on the Bar-On model. Intervention 2: Intervention group:  After random allocation, participants receive 10 individual sessions of 90-minute Intensive Short-Term Dynamic Psychotherapy (ISTDP). Intervention 3: Control Group: During the study period, participants receive no intervention and remain on the waiting list.</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:
Given the nature of the study, after de-identifying the data, only the portion related to the primary outcome of the study will be shared.

When:
Access will begin 9 months after the publication of the results.

To whom:
Only researchers affiliated with academic institutions and researchers associated with the Ministry of Education.

Conditions:
No scientific misconduct and no data manipulation.

Where to obtain:
Hussein Lotfi: PhD student in Psychology, researcher, and developer of the Emotional Intelligence Training Protocol. Email: lotfi6th@gmail.com
Dr. Seyed Mousa Tabatabaei: Primary supervisor. Email:s.mosatabatabaee@semnan.ac.ir
Dr. Mojtaba Rajabpour: Co-supervisor. Email:mj_rajabpour@yahoo.com
Dr. Hakimeh Aghaei: Advisory supervisor. Email: ha.aghae@gmail.com

How to obtain:
Request submission via the researcher’s email (Hussein Lotfi), consultation between the researcher and the supervisors/advisor, decision-making by the researcher and supervisors, and sharing of data/documents if deemed appropriate by the supervisors. The duration of this process is between one to two weeks.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Hussein Lotfi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 337, Alley 24, Azadi Blvd., Azadi Square</address>
        <city>Shahrud</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3617694631</zip>
        <telephone>+98 23 3233 3417</telephone>
        <email>lotfi6th@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Seye Musa Tabatabaee</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Psychology and Educational Sciences, Darband St.</address>
        <city>Mahdishahr</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3564111556</zip>
        <telephone>+98 23 3153 3010</telephone>
        <email>s.mosatabatabaee@semnan.ac.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Being employed in elementary school in one of the following positions: school principal, vice-principal, or teaching in one of the six grade levels of elementary education.
Absence of gastrointestinal diseases of physical origin confirmed by a specialist physician, history of cardiac disease, no history of substance abuse, and not being pregnant.</inclusion_criteria>
      <agemin>25 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Retirement, employment in administrative positions.
Suffering from the conditions and illnesses in parentheses (gastrointestinal diseases, heart disease, substance abuse, pregnancy).</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>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group:  After random assignment, participants receive 10 weekly sessions of 90-minute emotional intelligence training based on the Bar-On model.</i_keyword>
      <i_keyword>Intervention group:  After random allocation, participants receive 10 individual sessions of 90-minute Intensive Short-Term Dynamic Psychotherapy (ISTDP).</i_keyword>
      <i_keyword>Control Group: During the study period, participants receive no intervention and remain on the waiting list.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Experiential avoidance score based on the Multidimensional Experiential Avoidance Questionnaire (MEAQ). Timepoint: At the beginning of the study and one month after the end of the intervention. Method of measurement: Multidimensional Experiential Avoidance Questionnaire (MEAQ).</prim_outcome>
      <prim_outcome>Psychological Flexibility score. Timepoint: At the beginning of the study and one month after the end of the intervention. Method of measurement: Psychological flexibility questionnaire: AAQ-II (Acceptance and Action Questionnaire-II.</prim_outcome>
      <prim_outcome>Psychosomatic Symptoms score. Timepoint: At the beginning of the study and one month after the end of the intervention. Method of measurement: LaCourt Psychosomatic Questionnaire (LPSQ).</prim_outcome>
      <prim_outcome>Emotional Intelligence score. Timepoint: At the beginning of the study and two months after the end of the intervention. Method of measurement: Bar-On Emotional Intelligence 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>Shahrud County Education Department</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-08-11</approval_date>
        <contact_name>Research Ethics Committee of Islamic Azad University, Shahrud Branch</contact_name>
        <contact_address>Faculty of Medical Sciences, Islamic Azad University, Shahrud Branch, Khatam-al-Anbia Hospital, next to Amir Kabir High School, Univ. Blvd Shahrud Semnan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
