<?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>IRCT20251101067838N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-11-26</date_registration>
      <primary_sponsor>Jahrom University of Medical Sciences</primary_sponsor>
      <public_title>Studying the effect of using a mobile phone-based medication reminder program and sending educational SMS on medication adherence and quality of life of patients with Acute coronary syndrome After discharge</public_title>
      <acronym></acronym>
      <scientific_title>Studying the effect of using a mobile phone-based medication reminder program and sending educational SMS on medication adherence and quality of life of patients with Acute coronary syndrome discharge</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-11-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>66</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/87232</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In the present study, patients with acute coronary syndrome hospitalized in the cardiology wards of Peymanieh and Seyed Al-Shohada (AS) Hospitals affiliated with Jahrom University of Medical Sciences will be recruited using a convenience sampling method. Patients will be randomly assigned to the intervention group (33 participants) and the control group (33 participants) using the Random Allocation Software. The allocation of each patient will be done individually based on the randomization flowchart generated by the software, Blinding description: The study was single-blinded, meaning that the data collector (research assistant) was unaware of the participants’ group allocation (intervention or control) at each stage.</study_design>
      <phase>3</phase>
      <hc_freetext>Acute coronary syndrome.</hc_freetext>
      <i_freetext>Intervention 1: Intervention Group:  For patients in the intervention group, in addition to the routine training provided to all patients before discharge, the DaruYad medication-reminder application will be installed on their mobile phones. The DaruYad application was designed by the Biomedical Engineering Department, Faculty of Medical Sciences and Technologies, Science and Research Branch, Islamic Azad University.The various components of the DaruYad software include: the login section, the current medications section, access for the pharmaceutical representative to the patient’s dedicated page, searching the prescribed medication, selecting the medication from the available pharmaceutical company database, and determining the administration instructions for the selected drug.Within the application, the medication dose, dosing interval (every few hours), registration of the first administration time (hour and minute), start date (year, month, and day), dosage form (for example, if the medication is a tablet and half a tablet must be taken), the patient’s medication quota, an audio alarm, and a clear image of the medication’s appearance and specifications are displayed.In addition, patients will receive short reminder text messages for one month after discharge. Intervention 2: Control group: The control group will receive only the routine pre-discharge education provided in the ward, which includes recognizing warning signs, contacting emergency services immediately in case of symptom onset, rest and limitation of physical activity, indications for using nitroglycerin tablets and instructions for their administration, stress management, and appropriate dietary recommendations.</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>Justification or reason for indecision in sharing IPD is No further information is available</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Fakharzadeh jahromi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Unit 401, Pars Complex 26, Alley 29/3, Motahari St., Fars Province, Jahrom City</address>
        <city>Jahrom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7167758256</zip>
        <telephone>+98 71 5433 2908</telephone>
        <email>f.fakharzadeh@jums.ac.ir</email>
        <affiliation>Jahrom University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Rasoul Eslami Akbar</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Jahrom University of Medical Sciences, Motahari Boulevard, Jahrom</address>
        <city>jahrom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7414846199</zip>
        <telephone>+98 71 5434 0409</telephone>
        <email>eslamiakbarrasool@ gmail.com</email>
        <affiliation>Jahrom University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Definite diagnosis of acute coronary syndrome for the first time, confirmed by a cardiologist.
No major psychological disorders such as major depression, psychosis, etc.
Willingness of the patient to participate in the research.
Ability to read and write
Ability to use a mobile phone and possession of a personal smartphone capable of installing the medication reminder application used in the present study.
Ability to perform self-care activities, especially adherence to prescribed medications.
Age between 35 and 65 years
No hearing, vision, or other physical and sensory disabilities.
No addiction to drugs, alcohol, or psychoactive substances.
No memory-related disorders or dementia.
No participation in other educational programs or self-care intervention studies.
Patient’s acknowledgment of having adequate financial means or family/social support to obtain prescribed medications during the study period.</inclusion_criteria>
      <agemin>35 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Recurrence of acute and severe symptoms of the disease or acute complications of coronary syndrome (such as dysrhythmias and various types of heart blocks) requiring rehospitalization in intensive care units.
Development of cognitive or psychological disorders during the study.
Patient’s unwillingness to continue participation in the study.
Death of the patient.
Occurrence of acute events or crises affecting medication adherence and the patient’s quality of life, such as severe trauma, death of first-degree relatives, and similar situations.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>125.9</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Acute coronary</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention Group:  For patients in the intervention group, in addition to the routine training provided to all patients before discharge, the DaruYad medication-reminder application will be installed on their mobile phones. The DaruYad application was designed by the Biomedical Engineering Department, Faculty of Medical Sciences and Technologies, Science and Research Branch, Islamic Azad University.The various components of the DaruYad software include: the login section, the current medications section, access for the pharmaceutical representative to the patient’s dedicated page, searching the prescribed medication, selecting the medication from the available pharmaceutical company database, and determining the administration instructions for the selected drug.Within the application, the medication dose, dosing interval (every few hours), registration of the first administration time (hour and minute), start date (year, month, and day), dosage form (for example, if the medication is a tablet and half a tablet must be taken), the patient’s medication quota, an audio alarm, and a clear image of the medication’s appearance and specifications are displayed.In addition, patients will receive short reminder text messages for one month after discharge.</i_keyword>
      <i_keyword>Control group: The control group will receive only the routine pre-discharge education provided in the ward, which includes recognizing warning signs, contacting emergency services immediately in case of symptom onset, rest and limitation of physical activity, indications for using nitroglycerin tablets and instructions for their administration, stress management, and appropriate dietary recommendations.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Medication adherence. Timepoint: Before, immediately after the intervention, and two months after the intervention. Method of measurement: Morisky Medication Adherence Questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Quality of life. Timepoint: Before, immediately after the intervention, and two months after the intervention. Method of measurement: MacNew Heart Disease Health-related Quality of Life Questionnaire.</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>Jahrom University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-10-20</approval_date>
        <contact_name>Ethics Committee of Jahrom University of Medical Sciences</contact_name>
        <contact_address>Deputy for Research and TechnologyوAdministrative (Campus) Building,Jahrom University of Medical Sciences,End of Shahid Motahari Street,Jahrom, Fars Province, Iran jahrom Fars Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
