<?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>IRCT20260612069760N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-07-28</date_registration>
      <primary_sponsor>Ahvaz University of Medical Sciences</primary_sponsor>
      <public_title>The Effect of Targeted Nursing Care on Recovery of Cardiac Patients</public_title>
      <acronym></acronym>
      <scientific_title>The effect of nursing care based on Gordon's functional health model on length of hospitalization and quality of life in patients with Acute Coronary Syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-07-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/90932</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: Random allocation of participants to intervention and control groups will be performed using block randomization. For this purpose, blocks of a specified size (e.g., 4 or 6) will be formed to ensure a balanced number of participants in both groups throughout the study. For each block, a random sequence of letters (A for the intervention group and B for the control group) will be generated using specialized software. These sequences will then be applied consecutively to allocate participants.
To ensure allocation concealment and to prevent selection bias, the generated sequences will be written on cards and placed in opaque, sealed, and sequentially numbered envelopes. These envelopes will be kept by an individual who is independent of the enrollment and intervention processes. They will be opened in sequential order only after final confirmation of participant eligibility and completion of baseline assessments, at which point the participant's group assignment will be revealed.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Patients diagnosed with Acute Coronary Syndrome (ACS).</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Patients with acute coronary syndrome will receive routine hospital care plus a Gordon's Functional Health Patterns-based nursing care program. The intervention consists of a comprehensive 14-day structured nursing program based on the 11 functional health patterns, including patient education, counseling, nutritional management, physical activity guidance, medication adherence, stress management, and follow-up. Participants will also receive a follow-up telephone call three months after the intervention. Intervention 2: Control group: Control group: Patients with acute coronary syndrome will receive routine hospital care only. They will not receive the Gordon's Functional Health Patterns-based nursing care program. Outcomes will be assessed at the same time points as the intervention group: before the intervention, immediately after the intervention, and three months after the 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:
Only limited portions of the information pertaining to the original message or equivalent content may be disclosed.

When:
The access period will commence following the publication of the study results.

To whom:
For all people

Conditions:
Utilization of Gordon's Functional Health Pattern Model for the Enhancement of Patients' Quality of Life

Where to obtain:
Reputable Scientific Websites

How to obtain:
A systematic search was performed using the following keywords: Gordon, Quality of Life, and Acute Coronary Syndrome.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Neda Sayady</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>"Block 3, Golestan Female Student Dormitory, Golestan Boulevard"</address>
        <city>Ahvaz</city>
        <country1>American Samoa</country1>
        <zip>6135815751</zip>
        <telephone>986133112653</telephone>
        <email>aydakaraminia@gmail.com</email>
        <affiliation>Ahvaz University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Neda Sayady</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>"Golestan Expressway, Ahvaz Jundishapur University of Medical Sciences</address>
        <city>Ahvaz</city>
        <country1>American Samoa</country1>
        <zip>6135715794</zip>
        <telephone>986133110000</telephone>
        <email>aydakaraminia@gmail.com</email>
        <affiliation>Ahvaz University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>American Samoa</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Confirmed diagnosis of Acute Coronary Syndrome by a cardiologist based on the triple triad criteria.
Patients aged 18 years and older
Ability to read and write in Persian
Fully conscious and oriented to time and place
No history of cognitive or psychiatric disorders</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Patient's unwillingness to continue participation in the study for any reason
Deterioration of the participant's condition or death
Occurrence of any disease or injury that may affect the participant's functional independence during the study, such as CVA or spinal cord injuries.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>I24.9</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Acute ischemic heart disease, unspecified</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Patients with acute coronary syndrome will receive routine hospital care plus a Gordon's Functional Health Patterns-based nursing care program. The intervention consists of a comprehensive 14-day structured nursing program based on the 11 functional health patterns, including patient education, counseling, nutritional management, physical activity guidance, medication adherence, stress management, and follow-up. Participants will also receive a follow-up telephone call three months after the intervention.</i_keyword>
      <i_keyword>Control group: Control group: Patients with acute coronary syndrome will receive routine hospital care only. They will not receive the Gordon's Functional Health Patterns-based nursing care program. Outcomes will be assessed at the same time points as the intervention group: before the intervention, immediately after the intervention, and three months after the intervention.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Quality of life assessed using the Seattle Questionnaire before intervention, immediately after intervention, and three months post-intervention. Timepoint: Three months post-intervention. Method of measurement: Demographic Questionnaire, Seattle Angina Questionnaire (SAQ), Gordon's Functional Health Pattern Assessment Questionnaire.</prim_outcome>
      <prim_outcome>Length of hospital stay measured from admission to discharge. Timepoint: At discharge. Method of measurement: Length of stay is a quantitative and objective variable that, unlike quality of life, does not require a questionnaire or psychometric instrument. This variable is extracted directly from the patient's chart or medical records.</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>Ahvaz University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-06-07</approval_date>
        <contact_name>Ethics Committee of Ahvaz Jundishapur University of Medical Sciences</contact_name>
        <contact_address>Block 3, Golestan Female Student Dormitory, Golestan Boulevard Ahvaz Khuzestan American Samoa</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
