<?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>IRCT20260816070684N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-09-18</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>The effectiveness of mindfulness on self-esteem, resilience, and mental vitality</public_title>
      <acronym></acronym>
      <scientific_title>The effectiveness of mindfulness on self-esteem, resilience, and mental well-being in students with dyslexia.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-09-20</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/92914</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In this study, a complete randomization method with an allocation ratio of 1:1 is used, and the randomization unit is the individual. After preparing the final list of 30 participants, each individual is assigned a unique numerical identification code. Then, an individual independent of the intervention implementers and evaluators generates a random number for each code using Random Number Generator software, and the participants are sorted in ascending order based on these numbers. The first 15 people are assigned to the experimental group and the next 15 people are assigned to the control group sequentially; thus, the probability of each individual being assigned to each group is equal, and the allocation ratio in the two groups is equal, Blinding description: To control for bias, this study employs a design that blinds the outcome assessor and the data analyst. Following full ethical briefing and the signing of informed consent forms, participants and their parents remain unaware of the specific hypotheses and group assignments; however, complete perceptual blinding is not feasible given the behavioral and educational nature of the mindfulness sessions. Randomization is performed by an independent individual, and sessions are led by a separate instructor; consequently, the principal investigator and school staff remain unaware of student group assignments until the study concludes. Given the non-medical nature of the intervention, medical personnel play no role in the study. Outcome assessments—conducted at pre-test, post-test, and follow-up stages—are carried out by assessors who are entirely independent of the intervention team and unaware of group allocations. Similarly, the statistician receives raw data identified only by anonymous codes and remains blinded until the analysis process is complete. As the intervention poses no risk, the establishment of a data monitoring committee is not required, and the authors will finalize the manuscript only after the final unblinding.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Children with learning disabilities.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: The mindfulness training program will be based on the standard mindfulness protocol for children designed by Sample and Lee (2008; translated by Mashhadi et al., 2017). The sessions of this intervention will be conducted in 8 60-minute sessions (one session per week) in a group setting for the experimental group. Mindfulness training is an approach that aims to increase attention to the present moment, reduce anxiety and rumination, and develop emotional regulation skills by promoting sensory and physical awareness. It helps students with dyslexia manage their academic and emotional challenges by replacing automatic and stressful reactions with responses based on calm and acceptance, and achieve the promotion of self-esteem, resilience, and mental vitality. This approach has main educational axes that lead to improved self-control and enhanced concentration; These axes include: establishing a therapeutic relationship and introducing the concept of mindfulness and paying attention to the present moment through sensory exercises (such as the raisin exercise), strengthening conscious attention to the environment through stimulating the five senses, teaching conscious breathing as an anchor for achieving calm, increasing body awareness and relaxation through body scan exercises, identifying and accepting difficult emotions (stress, anxiety, sadness, and anger) without judgment, teaching strategies for overcoming academic procrastination and managing behavior, integrating mindfulness with physical activities and stretching movements, and finally consolidating skills, building a personal mindfulness toolbox, and summarizing what has been learned. The main emphasis of this program is to direct children's non-judgmental attention to internal and external experiences and replace anxious and procrastinating patterns with conscious, flexible, and focused behaviors. Intervention 2: Control group: They do not receive any intervention or treatment.</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 Participant data is completely confidential and I do not intend to publish it.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Salahshouri</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Daneshjo Square, Zagros Blvd.</address>
        <city>Izeh</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6391693627</zip>
        <telephone>+98 936 997 2805</telephone>
        <email>fatemesalahshouri19@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fatemeh Salahshouri</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Daneshjo Square, Zagros Blvd.</address>
        <city>Izeh</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6391693627</zip>
        <telephone>+98 936 997 2805</telephone>
        <email>fatemesalahshouri19@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Participants must be between 6 and 10 years of age.
Participants must have scored above the mean on the dyslexia questionnaire.
Both the participants and their parents/guardians must provide informed consent to participate in the study.</inclusion_criteria>
      <agemin>6 years</agemin>
      <agemax>10 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having physical illnesses that interfere with the intervention process.
Current use of psychiatric medications.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>F81.9</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Developmental disorder of scholastic skills, unspecified</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: The mindfulness training program will be based on the standard mindfulness protocol for children designed by Sample and Lee (2008; translated by Mashhadi et al., 2017). The sessions of this intervention will be conducted in 8 60-minute sessions (one session per week) in a group setting for the experimental group. Mindfulness training is an approach that aims to increase attention to the present moment, reduce anxiety and rumination, and develop emotional regulation skills by promoting sensory and physical awareness. It helps students with dyslexia manage their academic and emotional challenges by replacing automatic and stressful reactions with responses based on calm and acceptance, and achieve the promotion of self-esteem, resilience, and mental vitality. This approach has main educational axes that lead to improved self-control and enhanced concentration; These axes include: establishing a therapeutic relationship and introducing the concept of mindfulness and paying attention to the present moment through sensory exercises (such as the raisin exercise), strengthening conscious attention to the environment through stimulating the five senses, teaching conscious breathing as an anchor for achieving calm, increasing body awareness and relaxation through body scan exercises, identifying and accepting difficult emotions (stress, anxiety, sadness, and anger) without judgment, teaching strategies for overcoming academic procrastination and managing behavior, integrating mindfulness with physical activities and stretching movements, and finally consolidating skills, building a personal mindfulness toolbox, and summarizing what has been learned. The main emphasis of this program is to direct children's non-judgmental attention to internal and external experiences and replace anxious and procrastinating patterns with conscious, flexible, and focused behaviors.</i_keyword>
      <i_keyword>Control group: They do not receive any intervention or treatment.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Self-esteem. Timepoint: Before performing the intervention and two weeks after completion of the intervention. Method of measurement: Mavroli et al.'s Children's Self-Esteem Questionnaire (2008).</prim_outcome>
      <prim_outcome>Resilience. Timepoint: Before performing the intervention and two weeks after completion of the intervention. Method of measurement: Angar and Liebenberg Resilience Questionnaire (2009).</prim_outcome>
      <prim_outcome>Mental vitality. Timepoint: Before performing the intervention and two weeks after completion of the intervention. Method of measurement: Ryan and Frederick Mental Vitality Questionnaire (1997).</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>2026-07-28</approval_date>
        <contact_name>Behbahan Islamic Azad University Ethics Committee</contact_name>
        <contact_address>Shahid Bayani St., Amir Kabir Blvd. Behbahan Khouzestan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
