<?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>IRCT20190805044439N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-06-08</date_registration>
      <primary_sponsor>Bagheiat-allah University of Medical Sciences</primary_sponsor>
      <public_title>The effect of liaison nurse on patient recovery</public_title>
      <acronym></acronym>
      <scientific_title>Assessment of the liaison nurses role impact on outcomes in patients transited from the emergency department to the other wards</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-10-25</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/41337</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Not randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Other design features: Since few studies have been done in this area in Iran so far and no studies have been conducted in Iran regarding the presence of a liaison nurse in the emergency department and its role in patient outcomes. By using liaison nurse services in the emergency department, its role is to improve the performance indicators of the emergency department such as: length of stay in the emergency department, improvement and stabilization of vital signs, and patient satisfaction, reducing anxiety in patients. To examine. To take effective steps to reduce patient length of stay, increase patient satisfaction, reduce patient anxiety, improve and stabilize patients' vital symptoms, and ultimately improve the quality of care for these patients.</study_design>
      <phase>N/A</phase>
      <hc_freetext>The Impact of Liaison Nurses on Outcomes of Patients Transferred from Emergency Department to Other Ward in Selected Hospital.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group:  Interventional nurse  begins in the intervention group of 30 and includes training and accompanying them on the conditions of the ward (portable), ward nurses and how to access them, ward facilities, differences in ward conditions and facilities. The Emergency Department and the reasons for moving to the ward will provide patients and their companions with information as well as face-to-face and face-to-face education on the type of diet, the importance, amount and how to work in and out of bed. The bed receives adaptation to the new conditions and the new ward, and the patient is nurse-assisted and nurse assisted with care. The necessary items and safety items will be shipped to the destination during transportation. Intervention 2: Control group: Control group: Initially 30 patients will be included in the study who will receive only routine care in the ward, and data will be collected and collected by the control group, by monitoring and recording vital signs and assessing the rate. Patients' satisfaction and anxiety will be measured with the intended tools. Finally, both intervention and control groups will be evaluated and compared based on patient outcomes including: vital signs, length of stay, satisfaction rate, hospital anxiety score.</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 more information.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Abbas Ebadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Baqiyatallah Hospital, Molla Sadra Street, Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1435915371</zip>
        <telephone>+98 21 8248 3131</telephone>
        <email>Abadi1347@yahoo.com‏</email>
        <affiliation>Bagheiat-allah University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Abbas Ebadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Baqiyatallah Hospital, Molla Sadra Street, Tehran</address>
        <city>TEHRAN</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1435915371</zip>
        <telephone>+98 21 8248 3131</telephone>
        <email>ebadi1347@yahoo.com‏</email>
        <affiliation>Bagheiat-allah University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>All patients who have the necessary cooperation to intervene and evaluate.
Have the admission to the ward under consideration and the candidate to move to the other ward.
The patient is alert and aware of time, place and person.
Ability to understand and understand Persian language content
All patients aged 18-85 years.
The patient is breathing spontaneously and is not intubated or supported by a ventilator.</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>85 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>The occurrence of unpredictable events during the transfer process (such as cardiopulmonary arrest and resuscitation in the ward)
Not willing to continue cooperation
Transfer to other medical centers or early consent for discharge</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>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group:  Interventional nurse  begins in the intervention group of 30 and includes training and accompanying them on the conditions of the ward (portable), ward nurses and how to access them, ward facilities, differences in ward conditions and facilities. The Emergency Department and the reasons for moving to the ward will provide patients and their companions with information as well as face-to-face and face-to-face education on the type of diet, the importance, amount and how to work in and out of bed. The bed receives adaptation to the new conditions and the new ward, and the patient is nurse-assisted and nurse assisted with care. The necessary items and safety items will be shipped to the destination during transportation</i_keyword>
      <i_keyword>Control group: Control group: Initially 30 patients will be included in the study who will receive only routine care in the ward, and data will be collected and collected by the control group, by monitoring and recording vital signs and assessing the rate. Patients' satisfaction and anxiety will be measured with the intended tools. Finally, both intervention and control groups will be evaluated and compared based on patient outcomes including: vital signs, length of stay, satisfaction rate, hospital anxiety score.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Assessing the level of patient anxiety in the patient transfer process. Timepoint: It is performed in two stages. One is measured at the beginning of the study and before the intervention in the emergency department, and the next after the intervention and after the patient is transferred to the destination ward. Method of measurement: The Hospital Anxiety and Depression Questionnaire, designed by Zigmon and Snow White in 1983.</prim_outcome>
      <prim_outcome>Assessing patient satisfaction in the patient transfer process. Timepoint: It is performed in two stages. One is measured at the beginning of the study and before the intervention in the emergency department, and the next after the intervention and after the patient is transferred to the destination ward. Method of measurement: The Patient Satisfaction Questionnaire was developed in 1994 by Wolf et al. To assess patient satisfaction.</prim_outcome>
      <prim_outcome>The duration of the patient's stay in the emergency department. Timepoint: Transfer time to section. Method of measurement: From the time of admission of the patient in the emergency department to the time of transferring the patient to the ward that is registered in the patient's file, it is calculated as the length of hospitalization in the emergency department.</prim_outcome>
      <prim_outcome>Stabilization of vital signs of patients. Timepoint: Patients' vital signs are checked twice a day at the beginning of the study and twice a day in the morning and in the afternoon for 24 hours after transfer to the ward. Method of measurement: Monitoring device (to control blood pressure and the number of breaths and the number of pulses and the patient's temperature).</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>Bagheiat-allah University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-10-16</approval_date>
        <contact_name>Baqiyatallah University of Medical Sciences</contact_name>
        <contact_address>Sheikh Baha'i - Mulla Sadra tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
