<?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>IRCT20231002059585N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-01-26</date_registration>
      <primary_sponsor>Artesh University of Medical Sciences</primary_sponsor>
      <public_title>Investigating the effect of liaison nurse on satisfaction ,anxiety and medication compliance in cardiac patients</public_title>
      <acronym></acronym>
      <scientific_title>The effect of the role pf liaison nurse on anxiety ,satisfaction and medication adherence in cardiac patients referring to the emergency ward of selected Aja hospital in Tehran</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-02-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>38</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/72898</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Supportive, Randomization description: Simple random assignment(coin toss)Simple random allocation (tossing a coin), and sampling will be of an easy type (accessible), so if the coin is tossed and it lands on the tap, the first patient who goes to the emergency room who meets the conditions of the research is considered the intervention group and the next patient of the test, and vice versa, if it lands on the line, the second patient is the intervention and the first patient. The test is considered, and until the last sample, we consider an intervention patient and a test patient, respectively, until the end of the samples.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Cardiac patients referred to the emergency room who have a history of drug use.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Cardiac patients referred to the emergency room who do meet the conditions for the study were selected from the beginning of entering the emergency room, and after explaining the method and objectives of the study to them and their companions, written informed consent was obtained, and before the intervention, demographic and personal information was taken, and the anxiety questionnaire number 1 was placed in the patient's possession and completed, then the liaison nurse began to The intervention, which includes two parts of psychological support to reduce anxiety and increase the level of satisfaction and... and the other part of educational support and giving awareness about the disease, treatments, and the use of drugs, etc., is carried out, and then when being discharged or transferred to the inpatient department, the anxiety questionnaire 2 Next) it will be filled by the patient, then the patient will be monitored and supported by phone for 2 weeks. After 2 weeks, the medication  compliance questionnaire is asked and filled by the researcher over the phone. Intervention 2: Control group: In this group, only at the beginning of the selection of the patient who is willing to study, sufficient explanations are given to the patient about the method and objectives of the study, and first, written informed consent and demographic and personal information are obtained, and the anxiety questionnaire is filled in by the patient, and no intervention is performed during the discharge of the patient. After leaving the emergency department for hospitalization, the anxiety questionnaire and the satisfaction questionnaire are filled out, and then 2 weeks later, the medication compliance questionnaire is filled out by phone.</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:
spss file of data

When:
22/08/2024

To whom:
all people such as samples and researchers

Conditions:
In order to check the accuracy of the data and the analyzes performed, the data will be provided to the journal in which the article will be published. Apart from this, the research team does not consider other special conditions

Where to obtain:
By emailing the responsible author of the article: fatemehvafaee135@gmail.com                                           MOBILE:09126349447

How to obtain:
In order to check the accuracy of the data and the analyzes performed, the data will be provided to the journal in which the article will be published. Apart from this, the research team does not consider other special conditions

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatama Wafai</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Tehran, Azgol neighborhood, Asharghi Burj Hor, No. 12, Unit 23</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1695839830</zip>
        <telephone>+98 21 2637 4828</telephone>
        <email>fatemehvafaee135@gmail.com</email>
        <affiliation>Artesh University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Nahid Rajaei</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Shariati St., in front of Baharshiraz St., Kaj St., next to Army Family Hospital, Army School of Nursing</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1615116139</zip>
        <telephone>+98 21 7750 0929</telephone>
        <email>N.Rajai22@yahoo.com</email>
        <affiliation>Artesh University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age over 18and over 65 years old
Awere of time and place
Not having mental illness and not having cognitive problems(Based on self-report)
Going to the emergency room due to heart problems and taking heart medications</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Free cancellation of cooperation
Occurrence of unpredictable events during the transfer process(such as cardiorespiratory arrest and patient resuscitation)</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Cardiac patients referred to the emergency room who do meet the conditions for the study were selected from the beginning of entering the emergency room, and after explaining the method and objectives of the study to them and their companions, written informed consent was obtained, and before the intervention, demographic and personal information was taken, and the anxiety questionnaire number 1 was placed in the patient's possession and completed, then the liaison nurse began to The intervention, which includes two parts of psychological support to reduce anxiety and increase the level of satisfaction and... and the other part of educational support and giving awareness about the disease, treatments, and the use of drugs, etc., is carried out, and then when being discharged or transferred to the inpatient department, the anxiety questionnaire 2 Next) it will be filled by the patient, then the patient will be monitored and supported by phone for 2 weeks. After 2 weeks, the medication  compliance questionnaire is asked and filled by the researcher over the phone.</i_keyword>
      <i_keyword>Control group: In this group, only at the beginning of the selection of the patient who is willing to study, sufficient explanations are given to the patient about the method and objectives of the study, and first, written informed consent and demographic and personal information are obtained, and the anxiety questionnaire is filled in by the patient, and no intervention is performed during the discharge of the patient. After leaving the emergency department for hospitalization, the anxiety questionnaire and the satisfaction questionnaire are filled out, and then 2 weeks later, the medication compliance questionnaire is filled out by phone.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Anxiety. Timepoint: At least an hour. Method of measurement: Spielberger anxiety questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Satisfaction. Timepoint: From an hour to a day. Method of measurement: The satisfaction questionnaire of Wolf et al.</sec_outcome>
      <sec_outcome>Moriski medication adherence. Timepoint: two weeks. Method of measurement: Moriski medication adherence 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>Artesh University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-08-28</approval_date>
        <contact_name>دانشگاه علوم پزشکی ارتش</contact_name>
        <contact_address>تهران خیابان فاطمی غربی_خیابان شهید اعتماد زاده تهران Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
