<?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>IRCT20261017071459N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-10-30</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>The Effect of Mindfulness Training on Reducing Test Anxiety and Improving Quality of Life and Motivation Among Female Students</public_title>
      <acronym></acronym>
      <scientific_title>A Study of the effectiveness of mindfulness-based stress reduction therapy on test anxiety, perceived stress, quality of academic life, and motivational beliefs of female students with test anxiety in ninth grade</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-11-01</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>40</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/94139</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: The statistical population for this study consists of all ninth-grade female students suffering from test anxiety who visit the counseling center of the General Directorate of Education during the study's designated timeframe. A convenience sampling method will be employed to select the sample. Following the selection of 40 participants—based on the study's inclusion and exclusion criteria—they will be randomly assigned to either the "Mindfulness-Based Stress Reduction" group (intervention group) or the "waiting list" group (control group). Randomization will be conducted using a permuted-block design with varying block sizes (4 and 6) by an independent statistician who is not involved in the study's implementation. The randomization sequence will be generated using the RAND function in Microsoft Excel and placed into opaque, sealed, and numbered envelopes to ensure that neither the researcher nor the participants are aware of the allocation sequence (allocation concealment). The envelopes will be opened—revealing the assigned group—only at the time each participant enters the study. To ensure the equivalence of baseline variables (such as anxiety level and age) between the two groups, their distribution will be examined during the statistical analysis phase.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Test Anxiety.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Mindfulness-Based Stress Reduction. Session duration: 90 minutes. Total number of sessions: 8. Session frequency: Two sessions per week. Therapeutic tools employed: This intervention focuses on developing the capacity for present-moment awareness, non-judgmental acceptance, and emotional regulation. Key components include: formal and informal mindfulness practices, the "three-minute breathing space" exercise, guided group discussions, and the identification of negative automatic thoughts related to examinations. The content of the sessions is structured as follows: Session 1: Introductions among participants, administration of pre-tests, explanation of the rationale behind mindfulness-based therapy, exploration of the concept of exam-related stress and its connection to thoughts and bodily reactions, and instruction in mindful breathing. Session 2: Introduction to the "body scan" practice to enhance awareness of physical sensations and the somatic signs of exam-related stress and anxiety. Session 3: Mindful sitting practices, focusing on the breath as an anchor for attention, and strategies for managing mental distractions during study and examinations. Session 4: Identification of negative automatic thought patterns, maladaptive academic beliefs, and catastrophic thinking regarding grades and exams; practicing the perspective of viewing thoughts as "mental events" rather than absolute facts. Session 5: Working with challenging emotions and stress, fostering emotional acceptance—rather than struggling against anxiety—and practicing the "three-minute breathing space" technique for use during moments of acute anxiety. Session 6: Examining the mind-body connection in the context of academic pressures and expectations (stemming from oneself, family, and school), and managing them through mindful awareness. Session 7: Integrating mindfulness practices into actual study situations and exam days, and developing a personalized self-care plan. Session 8: Consolidating what has been learned, reviewing key techniques to ensure the continuity of practice, administering a post-test, and scheduling a follow-up assessment. Intervention 2: Control group: The control group will not receive any intervention during the conduct of the study; however, to prevent threats to the study's internal validity—such as compensatory rivalry or demoralization—they will receive the intervention after the data collection phase.</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>Undecided - It is not yet known if there will be a plan to make this available</results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Nazanin Amirjani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Opposite Keshavarz Street, Farhang Shahr, Golestan Highway</address>
        <city>Ahvaz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6134937333</zip>
        <telephone>+98 61 3334 8421</telephone>
        <email>n.amirjani@iau.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Nazanin Amirjani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Opposite Keshavarz Street, Farhang Shahr, Golestan Highway</address>
        <city>Ahvaz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6134937333</zip>
        <telephone>+98 61 3334 8421</telephone>
        <email>n.amirjani@iau.ir</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Ninth-grade girls, aged 14 to 15
Scoring one standard deviation above the mean on test anxiety</inclusion_criteria>
      <agemin>14 years</agemin>
      <agemax>15 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Unwillingness to participate in the research
A history of psychotic disorders, major depression, severe generalized anxiety disorders, or other clinical conditions requiring immediate medication or treatment.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>F41.1</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Generalized anxiety disorder</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Mindfulness-Based Stress Reduction. Session duration: 90 minutes. Total number of sessions: 8. Session frequency: Two sessions per week. Therapeutic tools employed: This intervention focuses on developing the capacity for present-moment awareness, non-judgmental acceptance, and emotional regulation. Key components include: formal and informal mindfulness practices, the "three-minute breathing space" exercise, guided group discussions, and the identification of negative automatic thoughts related to examinations. The content of the sessions is structured as follows: Session 1: Introductions among participants, administration of pre-tests, explanation of the rationale behind mindfulness-based therapy, exploration of the concept of exam-related stress and its connection to thoughts and bodily reactions, and instruction in mindful breathing. Session 2: Introduction to the "body scan" practice to enhance awareness of physical sensations and the somatic signs of exam-related stress and anxiety. Session 3: Mindful sitting practices, focusing on the breath as an anchor for attention, and strategies for managing mental distractions during study and examinations. Session 4: Identification of negative automatic thought patterns, maladaptive academic beliefs, and catastrophic thinking regarding grades and exams; practicing the perspective of viewing thoughts as "mental events" rather than absolute facts. Session 5: Working with challenging emotions and stress, fostering emotional acceptance—rather than struggling against anxiety—and practicing the "three-minute breathing space" technique for use during moments of acute anxiety. Session 6: Examining the mind-body connection in the context of academic pressures and expectations (stemming from oneself, family, and school), and managing them through mindful awareness. Session 7: Integrating mindfulness practices into actual study situations and exam days, and developing a personalized self-care plan. Session 8: Consolidating what has been learned, reviewing key techniques to ensure the continuity of practice, administering a post-test, and scheduling a follow-up assessment.</i_keyword>
      <i_keyword>Control group: The control group will not receive any intervention during the conduct of the study; however, to prevent threats to the study's internal validity—such as compensatory rivalry or demoralization—they will receive the intervention after the data collection phase.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Test Anxiety. Timepoint: 1. Pre-test (before the start of the intervention) 2. Post-test (immediately after the end of the intervention period) 3. One-month follow-up after the intervention. Method of measurement: Measurement will be conducted using Test Anxiety Inventory (Abolghasemi et al., 1375).</prim_outcome>
      <prim_outcome>Perceived Stress. Timepoint: 1. Pre-test (before the start of the intervention) 2. Post-test (immediately after the end of the intervention period) 3. One-month follow-up after the intervention. Method of measurement: Measurement will be conducted using the Perceived Stress Scale (Cohen et al., 1983).</prim_outcome>
      <prim_outcome>Academic Quality of Life. Timepoint: Measurement will be conducted using the Inley and Burke (1992) Academic Quality of Life Questionnaire. Method of measurement: 1. Pre-test (before the start of the intervention) 2. Post-test (immediately after the end of the intervention period) 3. One-month follow-up after the intervention.</prim_outcome>
      <prim_outcome>Motivational Beliefs. Timepoint: 1. Pre-test (before the start of the intervention) 2. Post-test (immediately after the end of the intervention period) 3. One-month follow-up after the intervention. Method of measurement: Measurement will be conducted using the Motivational Beliefs Questionnaire by Pintrich and DeGroot (1990).</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>2026-10-13</approval_date>
        <contact_name>Ethics Committee of the Islamic Azad University, Ahvaz Branch</contact_name>
        <contact_address>Opposite Keshavarz Street, Farhang Shahr, Golestan Highway Ahvaz Khouzestan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
