<?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>IRCT20261016071447N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-10-27</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>Comparison of the Effects of Interpersonal Psychotherapy and Cognitive Behavioral Therapy in Students with Suicidal Ideation.</public_title>
      <acronym></acronym>
      <scientific_title>Comparing the effectiveness of interpersonal psychotherapy interventions for adolescents (IPT-AST) and cognitive behavioral therapy (CBT) on academic retention, Entrapment, attitude to psychological help-seeking and belonging in students with suicidal thoughts.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-10-31</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/94148</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In this clinical trial, participants will first be selected from female secondary school students using purposive non-random sampling based on specific inclusion and exclusion criteria; eligible candidates—defined as those scoring at least 5 on the Beck Scale for Suicide Ideation—will be identified, and upon obtaining informed consent, they will be randomly assigned to the study groups using the `rand` function in Microsoft Excel.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Suicidal ideation.</hc_freetext>
      <i_freetext>Intervention 1: Intervention Group 1 receives the Interpersonal Psychotherapy for Adolescents program (Young, Mufson, &amp; Schuler, 2016) over 10 weekly sessions. The content of the sessions includes the assessment of significant interpersonal relationships, communication analysis, communication strategies for improving relationships, role-playing, and the application of these strategies to real-life situations. Intervention 2: Intervention Group 2 receives the short-term cognitive-behavioral program developed by Bryan and Rudd (2018), delivered in 10 weekly sessions. The content of these sessions covers emotion regulation, cognitive flexibility, crisis management, weakening the belief system supporting suicide, and relapse prevention. Intervention 3: Control group: They receive standard school services and remain on the waiting list. Once the study is concluded, the intended treatment will be provided to this group.</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 There is no further information.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Faezeh Mirzaei</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Omid 3 Alley, Alborz 56, Tehran Street</address>
        <city>Qaem Shahr</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4761857313</zip>
        <telephone>+98 11 4248 2293</telephone>
        <email>faezeh2567@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Ghodratollah Abbasi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Islamic Azad University of Sari, Farahabad Road</address>
        <city>Sari</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4661611691</zip>
        <telephone>+98 11 3444 5787</telephone>
        <email>gh_abbasi@iausari.ac.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Being in the 13 to 18 age range
Enrolled in lower or upper secondary education at schools in the city of Qaem Shahr
Score 5 or higher on the Beck Suicidal Thought Scale
Not receiving other similar psychological or psychiatric interventions concurrently during the conduct of the research
Submission of informed consent by the student and parents</inclusion_criteria>
      <agemin>13 years</agemin>
      <agemax>18 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Must not suffer from severe psychiatric disorders (such as psychosis or bipolar disorder).
Should not simultaneously receive other psychological treatments or pharmacotherapy.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>R45.8</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Other symptoms and signs involving emotional state. Suicidal ideation (tendencies)</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention Group 1 receives the Interpersonal Psychotherapy for Adolescents program (Young, Mufson, &amp; Schuler, 2016) over 10 weekly sessions. The content of the sessions includes the assessment of significant interpersonal relationships, communication analysis, communication strategies for improving relationships, role-playing, and the application of these strategies to real-life situations.</i_keyword>
      <i_keyword>Intervention Group 2 receives the short-term cognitive-behavioral program developed by Bryan and Rudd (2018), delivered in 10 weekly sessions. The content of these sessions covers emotion regulation, cognitive flexibility, crisis management, weakening the belief system supporting suicide, and relapse prevention.</i_keyword>
      <i_keyword>Control group: They receive standard school services and remain on the waiting list. Once the study is concluded, the intended treatment will be provided to this group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Academic persistence score in the Martin and Marsh questionnaire. Timepoint: Before the intervention, after the intervention, and one month after the end of the intervention. Method of measurement: Martin and Marsh’s (2008) 6-Item Academic Resilience Scale.</prim_outcome>
      <prim_outcome>Score for the feeling of being trapped on the Gilbert and Allan questionnaire; Beurs et al. Timepoint: Before the intervention, after the intervention, and one month after the end of the intervention. Method of measurement: Gilbert and Allen’s 16-item questionnaire (1998); Beurs et al.’s 4-item questionnaire (2020).</prim_outcome>
      <prim_outcome>Score for Attitude Toward Seeking Psychological Help. Timepoint: Before the intervention, after the intervention, and one month after the end of the intervention. Method of measurement: Fischer and Farina’s Attitudes Toward Seeking Professional Psychological Help Scale (1995).</prim_outcome>
      <prim_outcome>Belonging Score. Timepoint: Before the intervention, after the intervention, and one month after the end of the intervention. Method of measurement: Van Arden et al.’s 15-Item Interpersonal Needs Assessment Questionnaire (2012).</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>2026-07-14</approval_date>
        <contact_name>Islamic Azad University - Sari Branch (Research Ethics Committee)</contact_name>
        <contact_address>7th  Azad University, kilometer 7 of Darya Road (Farahabad) Sari Mazandaran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
