<?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>IRCT20240407061438N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-06-09</date_registration>
      <primary_sponsor>Mashhad University of Medical Sciences</primary_sponsor>
      <public_title>Investigating The Effect of The Educational-Supportive Program on The Quality of Recovery and Satisfaction with The Quality of Patient Care</public_title>
      <acronym></acronym>
      <scientific_title>Investigating The Effect of The Educational-Supportive Program on The Quality of Recovery and Satisfaction with The Quality of Care of Patients Undergoing Thoracotomy due to Hydatid Cyst.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-06-09</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>70</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/76397</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Sampling will be Available with a Time Block with Random Allocation Generated by SPSS Software to Two Control and Test Groups. Code A Corresponds to The Test Group and Code B Corresponds to The Control Group and to Hide The Allocation, it will be Kept in a Sealed Envelope. After Ensuring The Eligibility of Each Person, The Door of the Envelope will be Opened and According to That Sequence will be Allocated to The Relevant Group. In Order to Prevent the Dissemination of Information, After Assigning The First Research Unit to The Test Group, as Long as The Patients Selected for The Test Group are Present in The Ward, no Sampling will be done for The Control Group, and After The Discharge of The Patients of The Test Group, Sampling will be done. It will be done for The Control Group. The Control Group will be Treated in The Same way and as Long as The Patients of The Control Group Were Present in The Ward, No Sample will be Assigned to The Test Group. This Process will Continue Until The Completion of Sampling for Two Groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Hydatid cyst disease.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: For the people in the intervention group, an educational-support program will be implemented from the beginning of their hospitalization and the day before the surgery in the hospital, in which, in addition to introducing and expressing sympathy and drawing the patient's attention, the patient will be given information about the course of the disease and surgical treatment, and a comprehensive pamphlet. which is prepared based on the educational needs of the patients and is provided to the patient. Exercises and techniques such as motivational spirometry will also be taught in the form of face-to-face demonstration and training with the patient. The contact number of the researcher is also provided to the patient. It is possible for the patient to share the ambiguities with the researcher at specific times in the morning and evening during the days of hospitalization. The control group receives the usual hospital care and training. Intervention 2: Control group: The control Group Receives The Usual Care and Education of The Hospital, Which Usually What is done for these Patients in The Hospital Environment is that almost no Educational Program is Planned or Carried out for The Patients and The Nurses and The Treatment Team Spend their Time They Perform Therapeutic Measures such as giving Medicine and other Routine Measures. At the End of the Fifth Day after The Intervention and after Ccollecting The Questionnaires, an Educational Pamphlet Related to Post-Surgery Care and Training and Care needed after Discharge is given to The Patient in order to Appreciate his Participation in The Research.</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:
All the data obtained from this research will be shared after completion.

When:
Access to the data will be possible 3 months after the results are published.

To whom:
These data will be used for researchers working in academic and scientific institutions as well as for patients with hydatid cysts.

Conditions:
The data obtained from this research can be used in other scientific studies.

Where to obtain:
Copying (in any way) either from the full text or from the extracts is possible only with the coordination of the supervisor and the registered author and according to the instructions provided by the Central Library of Mashhad University of Medical Sciences. Details can be accessed through the relevant faculty library. The use of the thesis in articles or any scientific writing is subject to citing the source in compliance with the Mashhad University of Medical Sciences publishing regulations. Fatemeh Hajiabadi: HajiabadiF@mums.ac.ir,Kowsar Moslemi: Moslemik4002@mums.ac.ir

How to obtain:
The applicant should send an email to the responsible author and register his request. After verifying the correctness of the information of the mentioned person, the required content will be provided to him by mentioning the source.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Haji Abadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Educational Complex of Shahid Dr. Kharazmi, University Campus, East Gate of Ferdowsi University of Mashhad, Azadi Square, Mashhad, Razavi Khorasan</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9137913199</zip>
        <telephone>+98 51 3859 1511</telephone>
        <email>Hajiabadif@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Kowsar Moslemi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Educational complex of Shahid Dr. Kharazmi, University Campus, East Gate of Ferdowsi University of Mashhad, Azadi Square, Mashhad, Razavi Khorasan</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9137913199</zip>
        <telephone>+98 51 3859 1511</telephone>
        <email>moslemik4002@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Definitive Diagnosis of Hydatid cyst
Candidate for Thoracotomy Surgery Due to Hydatid Cyst
Informed Consent of The Patient to Participate in The Study
Full Consciousness and Being Aware of Place and Time
Age between 18-65 years
Not Having Hearing Problems (sitting fully Despite The Use of Assistive Devices) and Vision (Ability to Read a Newspaper at a Distance of 30cm with Glasses)
Ability to Read and Write
No History of Mental Disorders
Need Surgery
Not Having Employment as a Member of the Treatment Staff
No Underlying Disease (Asthma, Empyema, Lung Cancer, Tuberculosis, etc.)</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Death of The Patient
The Patient's GCS Drops so that he/she is Unable to Communicate
Unwillingness to Continue Cooperation in Conducting Research at any Stage
Participation in Similar Training Courses
Previous History of Heart and Lung Surgery</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>B67.1</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Echinococcus granulosus infection of lung</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: For the people in the intervention group, an educational-support program will be implemented from the beginning of their hospitalization and the day before the surgery in the hospital, in which, in addition to introducing and expressing sympathy and drawing the patient's attention, the patient will be given information about the course of the disease and surgical treatment, and a comprehensive pamphlet. which is prepared based on the educational needs of the patients and is provided to the patient. Exercises and techniques such as motivational spirometry will also be taught in the form of face-to-face demonstration and training with the patient. The contact number of the researcher is also provided to the patient. It is possible for the patient to share the ambiguities with the researcher at specific times in the morning and evening during the days of hospitalization. The control group receives the usual hospital care and training</i_keyword>
      <i_keyword>Control group: The control Group Receives The Usual Care and Education of The Hospital, Which Usually What is done for these Patients in The Hospital Environment is that almost no Educational Program is Planned or Carried out for The Patients and The Nurses and The Treatment Team Spend their Time They Perform Therapeutic Measures such as giving Medicine and other Routine Measures. At the End of the Fifth Day after The Intervention and after Ccollecting The Questionnaires, an Educational Pamphlet Related to Post-Surgery Care and Training and Care needed after Discharge is given to The Patient in order to Appreciate his Participation in The Research</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The Quality of Patients' Recovery. Timepoint: Measuring The Quality of Recovery of Patients on The First Day After Surgery, 3 Days After Surgery and The Fifth Day After Surgery. Method of measurement: Recovery Quality Questionnaire (QOR-40).</prim_outcome>
      <prim_outcome>Satisfaction with The Quality of Patient Care. Timepoint: Measuring Satisfaction with The Quality of Patient Care at The End of The Fifth Day of Hospitalization. Method of measurement: Patient Satisfaction Wolf Instrument (PSI).</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>2024-05-11</approval_date>
        <contact_name>Nursing and Midwifery Faculty Committee - Mashhad University of Medical Sciences</contact_name>
        <contact_address>Educational complex of Shahid Dr. Kharazmi, University Campus, East Gate of Ferdowsi University of Mashhad, Azadi Square, Mashhad, Razavi Khorasan Mashhad Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
