<?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>IRCT20251223068424N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-07-11</date_registration>
      <primary_sponsor>Shiraz University of Medical Sciences</primary_sponsor>
      <public_title>Comparison of the Effectiveness of an AI-Driven Automated Guidance-Based Educational Intervention versus a Social Network-Based Educational Intervention</public_title>
      <acronym></acronym>
      <scientific_title>Comparing the Effectiveness of an AI-Driven Automated Guidance Educational Intervention versus a Social Network-Based Educational Intervention on cellphone addiction and Social relational Quality among Dormitory-Residing Nursing Students</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-07-26</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/91434</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: Sampling method: Nursing students living in the dormitory across various academic semesters will be selected using a table of random numbers and subsequently assigned to one of three groups based on a block randomization scheme (block size of 6) generated by software. To this end, nursing students in semesters 3 through 6 will first be selected, and each will be assigned a number. A table of random numbers will be used to select these individuals. Once an individual is selected, they will be assigned to one of the three groups based on pre-prepared block randomization sequences (block size of 6) contained in sealed envelopes. Allocation Concealment Method
After the statistician generates the sequence of random blocks, the sequence is placed in sealed, numbered envelopes. Upon selecting a participant, the research assistant opens the envelopes sequentially to assign the individual to one of the three groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Students' dormitory.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: This study aims to reduce cellphone addiction by using intervetional content generated by an artificial intelligence system (ChatGPT). To ensure intervention consistency and enhance the internal validity of the study, participants do not interact directly with the AI system. Instead, all prompts and AI-generated responses are developed, reviewed, and finalized before the study begins and are provided identically to all participants.The researcher is responsible for designing the intervention, developing standardized prompts, generating and standardizing AI responses, and monitoring the implementation of the intervention. Participants use the pre-prepared materials to select the recommended behavioral strategies and apply them in their daily lives.The intervention is conducted over a four-week period and includes an initial orientation session, provision of a participant manual, implementation of a cellphone addiction reduction program, daily or weekly activity recording, standardized weekly feedback, and monitoring of adherence by the researcher assistant. During the first week, participants select and implement at least three behavioral strategies from a set of pre-designed options, including limiting mobile phone use, disabling unnecessary notifications, scheduling phone-free periods, engaging in alternative non-digital activities, and practicing brief mindfulness exercises.At the end of the fourth week, a post-intervention assessment is conducted to evaluate changes in cellphone addiction. The use of standardized prompts and fixed AI-generated responses for all participants ensures complete standardization of the intervention, eliminates variability associated with dynamic AI responses, and maintains consistency in the content, intensity, and quality of the intervention. Intervention 2: Intervention group: Social network-Based Training Group: The intervention is delivered via a social network accessible in Iran, utilizing a series of MP4 video files designed for micro-teaching. The research team conducts this four-week training program according to a per-established schedule. Each video file lasts between 3 and 10 minutes, ensuring ease of uploading and downloading on the social network. Additionally, the files are designed to be small in size so they can be easily opened on mobile phones with limited storage capacity. Intervention 3: Control group: This group receives no intervention.</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:
Primary outcomes would be shared.

When:
Starting 6 months after publication article

To whom:
People and researchers working in academic institutions

Conditions:
Data are provided for information only.

Where to obtain:
Data is available via email rambodma@gmail.com.

How to obtain:
Data is available via email rambodma@gmail.com.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Masoume Rambod</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Zand Street, Namazi Square. School of Nursing Midwifery, Shiraz</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>71936–13119</zip>
        <telephone>+98 71 3677 4254</telephone>
        <email>rambodma@gmail.com</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Masoume Rambod</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Nursing and Midwifery University, Namazee Sq, Zand Ave, Shiraz</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7193613119</zip>
        <telephone>+98 71 3647 4258</telephone>
        <email>rambodma@gmail.com</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>1)	Being a nursing student at Shiraz University of Medical Sciences in the city of Shiraz, 2)	Being a student in the 3rd to 6th semester of study, 3)	Residing in the dormitory for at least four consecutive days per week, 4)	Willingness to participate in research, 5)	Having been a student at Shiraz University of Medical Sciences since the beginning of their studies</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>30 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Transfer or visiting students
Missing no more than 5 sessions of the one-month course
Facing a crisis (death of a family member, divorce, etc.) during the study period</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Y92.16</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>School dormitory as the place of occurrence of the external cause</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: This study aims to reduce cellphone addiction by using intervetional content generated by an artificial intelligence system (ChatGPT). To ensure intervention consistency and enhance the internal validity of the study, participants do not interact directly with the AI system. Instead, all prompts and AI-generated responses are developed, reviewed, and finalized before the study begins and are provided identically to all participants.The researcher is responsible for designing the intervention, developing standardized prompts, generating and standardizing AI responses, and monitoring the implementation of the intervention. Participants use the pre-prepared materials to select the recommended behavioral strategies and apply them in their daily lives.The intervention is conducted over a four-week period and includes an initial orientation session, provision of a participant manual, implementation of a cellphone addiction reduction program, daily or weekly activity recording, standardized weekly feedback, and monitoring of adherence by the researcher assistant. During the first week, participants select and implement at least three behavioral strategies from a set of pre-designed options, including limiting mobile phone use, disabling unnecessary notifications, scheduling phone-free periods, engaging in alternative non-digital activities, and practicing brief mindfulness exercises.At the end of the fourth week, a post-intervention assessment is conducted to evaluate changes in cellphone addiction. The use of standardized prompts and fixed AI-generated responses for all participants ensures complete standardization of the intervention, eliminates variability associated with dynamic AI responses, and maintains consistency in the content, intensity, and quality of the intervention.</i_keyword>
      <i_keyword>Intervention group: Social network-Based Training Group: The intervention is delivered via a social network accessible in Iran, utilizing a series of MP4 video files designed for micro-teaching. The research team conducts this four-week training program according to a per-established schedule. Each video file lasts between 3 and 10 minutes, ensuring ease of uploading and downloading on the social network. Additionally, the files are designed to be small in size so they can be easily opened on mobile phones with limited storage capacity.</i_keyword>
      <i_keyword>Control group: This group receives no intervention.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Cellphone addiction. Timepoint: Before and after the intervention. Method of measurement: Cell phone addiction scale.</prim_outcome>
      <prim_outcome>Social relational quality. Timepoint: Before and after the intervention. Method of measurement: Social relations quality scale.</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>Shiraz University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-07-07</approval_date>
        <contact_name>Research Ethics commitees of Shiraz University of Medical Sciences</contact_name>
        <contact_address>Seventh floor, Central Building of Shiraz University of Medical Sciences, Zand St. Shiraz Fars Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
