<?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>IRCT20191224045878N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-02-19</date_registration>
      <primary_sponsor>Mashhad University of Medical Sciences</primary_sponsor>
      <public_title>The effect of Phase I Rehabilitation on the Delirium in Cardiac Surgery Patients</public_title>
      <acronym></acronym>
      <scientific_title>The effect of Phase I Cardiac Rehabilitation on the Rate of Delirium in Patients After Coronary Arteyry Bypass Graft Surgery</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-09-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/44838</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: In this Research, Inclusion of research units in the Study, The Method is Available and Random Allocation. Random Sequence Tool is SPSS. Random Sequence Was Prepared as a Table.It was Kept in an envelope.After making sure everyone is eligible, Envelope door Opened And The Sequence was assigned to that Group.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Coronary Artery Bypass Graft.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Individuals find the phase of a cardiac rehabilitation based on a Ministry of Health instruction that consists of three parts, including: 1. Exercise training and control by the researcher; 2. Discussion with the patient; 3. The patient was encouraged to perform activities for the intervention group. Exercise should be performed two to three times a day for at least 20 minutes and a maximum of 30 minutes. Then, according to the protocol of the Ministry of Health for 15 to 20 minutes, chest physiotherapy was performed. After chest physiotherapy, depending on whether the patient was in a supine position, sitting or standing, appropriate exercises were performed for the patient. At each exercise session, about 5 to 10 minutes to warm up, 5 to 10 minutes to cool and 20 to 30 minutes to exercise. Chest physiotherapy was given 15 to 20 minutes per session. In addition, diaphragmatic breathing training was performed face-to-face with the aid of image and shape, and the subjects performed exercise at least once a day in the presence of the researcher, and the next time, the patient performed the exercise alone. And to control gestures, the researcher was assisted in various shifts to monitor her performance as well as the accuracy of the exercise. In step two, the benefits of the cause and the disadvantages and overall self-care were described to the patient. Possible questions and uncertainties about surgery, diet, medications, post-operative rest, risk factors control, time to start daily activities, and marital relationships were answered and the patient was asked about any concerns and concerns. The researcher points out. In step three, the patient was used to encourage verbal communication and positive feedback to him and his family, such as good, effective, excellent in the presence of the patient. This rehabilitation started from the end of the endotracheal tube and continued for 5 to 7 days until the end of the open heart session. The control group received routine nursing interventions in the ward and in both the control and intervention groups, the scale (Nicham) was completed, measured and compared daily to assess the incidence of delirium at the same time. Intervention 2: Control group: In addition to receiving routine care, at the end of two weeks, a control booklet was administered to patients in the control group.</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:
Presentation of research findings in seminars, conferences, and publication of articles extracted from research in domestic and overseas journals, all hospitals, and even other departments, especially after surgical operations requiring the use of specific medications following psychologic complications. Have surgery, be used As well as researchers who intend to conduct research on the subject.

When:
Start of course available 6 months after printing results

To whom:
Share the results of the research with other researchers for further research

Conditions:
Used in all hospitals and even in other wards, especially after surgeries that require the use of specific medications in the aftermath of psychologically induced complications.

Where to obtain:
Visit to Mashhad School of Nursing and Midwifery

How to obtain:
After the email is sent to the scientific respondent, the accountability process begins

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Kolsoom Parnan Emamverdi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faramarz     Abbassi Street, 9 Faramarz Abbassi Street, No. 76</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9164889119</zip>
        <telephone>+98 51 3415848</telephone>
        <email>parnanek951@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Kolsoom Parnan Emaverdi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faramarz Abbassi Street, 9 Faramarz Abbassi Street, No. 76</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9164889119</zip>
        <telephone>+98 51 3414858</telephone>
        <email>parnanek951@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Be in a Group over the 18 Years
Do not use the Psychiatric or Antirelaxant Medications
Do not have a Histiry of Heart Surgery
Do not have a Movement Problem
Do not have a History of Delirium
Having a Score 0 From RASS means the patients is calm and relax and able to cooperative with researcher
Do not have a Known psychiatric Disease</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>F05.8</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Postoperative Delirium</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Individuals find the phase of a cardiac rehabilitation based on a Ministry of Health instruction that consists of three parts, including: 1. Exercise training and control by the researcher; 2. Discussion with the patient; 3. The patient was encouraged to perform activities for the intervention group. Exercise should be performed two to three times a day for at least 20 minutes and a maximum of 30 minutes. Then, according to the protocol of the Ministry of Health for 15 to 20 minutes, chest physiotherapy was performed. After chest physiotherapy, depending on whether the patient was in a supine position, sitting or standing, appropriate exercises were performed for the patient. At each exercise session, about 5 to 10 minutes to warm up, 5 to 10 minutes to cool and 20 to 30 minutes to exercise. Chest physiotherapy was given 15 to 20 minutes per session. In addition, diaphragmatic breathing training was performed face-to-face with the aid of image and shape, and the subjects performed exercise at least once a day in the presence of the researcher, and the next time, the patient performed the exercise alone. And to control gestures, the researcher was assisted in various shifts to monitor her performance as well as the accuracy of the exercise. In step two, the benefits of the cause and the disadvantages and overall self-care were described to the patient. Possible questions and uncertainties about surgery, diet, medications, post-operative rest, risk factors control, time to start daily activities, and marital relationships were answered and the patient was asked about any concerns and concerns. The researcher points out. In step three, the patient was used to encourage verbal communication and positive feedback to him and his family, such as good, effective, excellent in the presence of the patient. This rehabilitation started from the end of the endotracheal tube and continued for 5 to 7 days until the end of the open heart session. The control group received routine nursing interventions in the ward and in both the control and intervention groups, the scale (Nicham) was completed, measured and compared daily to assess the incidence of delirium at the same time.</i_keyword>
      <i_keyword>Control group: In addition to receiving routine care, at the end of two weeks, a control booklet was administered to patients in the control group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Delirium. Timepoint: Since the End of the Endotracheal Tube Up to 5 to 7 days after ُSurgery. Method of measurement: Neecham Tool.</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>Mashhad University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-10-25</approval_date>
        <contact_name>Ethics committee of Mashhad University of Medical Sciences</contact_name>
        <contact_address>Intersection Doctorate, Ibn Sina St, Mashhad Mashhad Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
