<?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>IRCT20180519039711N8</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-08-26</date_registration>
      <primary_sponsor>Arak University of Medical Sciences</primary_sponsor>
      <public_title>The effect of an electronic software based on nursing diagnoses on the amount of quality and nursing care missed by students and nurses working in teaching hospitals.</public_title>
      <acronym></acronym>
      <scientific_title>The effect of an electronic software based on Nanda's standard nursing diagnoses on the amount of quality and nursing care missed by students and nurses working in teaching hospitals</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-08-31</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/78278</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Health service research, Other design features: The present study is a production study in terms of its purpose, application and execution method. This study will be carried out in two separate phases as follows: first stage: Compilation and validation of electronic software content based on Nanda's standard nursing diagnoses, which includes the following 4 phases: First phase: needs assessment Today, one of the main challenges of the health care system is the increase in the number of patients visiting hospitals, which requires complex processes and care. Sometimes these processes are forgotten due to the excessive work load of nurses and affect the quality of appropriate, complete and comprehensive services provided by nurses. Currently, the nursing process as a standard that prevents forgetting the care provided and reducing the quality of nursing care is not given much attention by nursing students and professors in higher education centers. This is while providing care with the traditional routine method and not using the professional nursing process as a guide and standard care strategy can lead to the degradation of nursing from a scientific and practical point of view, reducing the quality of care services and providing one-dimensional care. . According to the experience of master's degree and doctorate in nursing, educational and clinical records, as well as the executive positions of the main owners of the process, as well as the colleagues of the research team, the initial idea of ​​this project was formed as an effective strategy in clinical education and a support assistant for the selection of nursing diagnoses. The standard and promotion of quality nursing care and reduction of lost care. The second phase: formation of the expert panel team The specialized team for deciding the content of the application program includes the research team and experienced and experienced professors in the field of nursing and the application of software in the field of nursing and nurses working in the special care department of teaching hospitals affiliated to Arak University of Medical Sciences who have work experience. are older than 6 months, they will be selected. The third phase: preparing the educational content of the software In this phase, the educational content of the software will be designed and compiled under the supervision of the expert panel team members during various meetings. It will be used for content creation of nursing diagnoses based on the latest list of Nanda nursing diagnoses 2021-2023, focusing on common signs and symptoms in various diseases. In the next step, the NOC &amp; NIC list will be used to design the care plan for planning and nursing measures. The fourth phase: design and development of electronic software This phase will be designed and implemented by the specialized software and informatics nursing team. At this stage, the different menus of the software; It will include signs and symptoms of the disease, nursing diagnosis and care plan, and tools to measure the quality of care provided and nursing care lost. second stage: At this stage, after designing and developing the electronic software in the first stage, a study was carried out to determine the effectiveness of the electronic program on a number of nursing students and nurses working in the special care department of teaching hospitals affiliated to Arak University of Medical Sciences. will be. This study will be a clinical trial with the design of two groups before and after. In this study, the effect of electronic software based on Nanda standard nursing diagnoses on the quality of nursing care and missed nursing care in nursing students and nurses working in the special care department of teaching hospitals affiliated to Arak University of Medical Sciences will be investigated. . The research units will be selected as available and will be randomly assigned in two intervention and control groups, Randomization description: The method of random selection of the group of nursing students:
First, a list of the names of the nursing intern students and their groupings will be received from the director of the nursing department of Arak University of Medical Sciences. In the next step, each group of students will be assigned a number and will be thrown into a container. The first group that comes out of the container will be placed in the intervention and control group by tossing a coin using a simple tap or line randomization model. In this way, if a coin comes up, that group will be in the intervention group, and if a line comes up, that group will be in the control group. The other groups will be placed in the control and intervention groups, respectively, based on the sequence of leaving the container.
The method of random selection of the group of nurses:
The group of nurses will be selected as available and will be randomly assigned to two intervention and control groups using the alternative block randomization technique. 6 blocks with 10 modes will be used. The letter A will represent the participant of the intervention group and the letter B will represent the participant of the control group. The samples will be selected in the intervention and control groups based on the sequence of entry and according to the block pattern and will be assigned to the intervention and control groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>The subject of the research does not include the disease.</hc_freetext>
      <i_freetext>Intervention group: During the study, the developed software will be available to the intervention groups (nurses and nursing students) (to prevent the content of the designed program from being disseminated to other students and nurses of the control group and to prevent the creation of information leakage of the software in such a way It will be designed to be installed in each mobile phone with only one password so that other people cannot use it) and they will provide their care to patients based on the developed program, and the control group will provide care to patients based on the conditions of the internship routine. will give Information will be collected using quality nursing care questionnaires and the two-part questionnaire of Kalish and Williams on a daily basis in the designed software..</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 potential data can be shared after identifying individuals requesting research information.

When:
It can be accessed after 2025/08/23.

To whom:
Researchers working in academic and scientific institutions and anyone who wants to access the data and details of researchers' research.

Conditions:
Researchers working in academic and scientific institutions and anyone who wants to access the data and details of researchers' research. Please mention in your request for what purpose you want to use the sources and data from our research.

Where to obtain:
Please contact Miss. Fatemeh Moghadasi at Arak University of Medical Sciences.
Email:fatemehmoghadasi03@gmail.com 
contact number: 09184879389.

How to obtain:
Please contact Miss. Fatemeh Moghadasi at Arak University of Medical Sciences.
Email:fatemehmoghadasi03@gmail.com 
contact number: 09184879389.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Moghadasi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>3rd floor, corner of Nizamzadeh Alley, Shahid Abdullahi Alley, Abuzar Street</address>
        <city>Arak</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3814187476</zip>
        <telephone>+98 86 3221 9231</telephone>
        <email>fatemehmoghadasi03@gmail.com</email>
        <affiliation>Arak University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fatemeh Moghadasi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>3rd floor, corner of Nizamzadeh Alley, Shahid Abdullahi Alley, Abuzar Street</address>
        <city>Arak</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3814187476</zip>
        <telephone>+98 86 3221 9231</telephone>
        <email>fatemehmoghadasi03@gmail.com</email>
        <affiliation>Arak University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Entry criteria for nursing students: 1) Willingness to participate in the study
2) Be a nursing internship student and have no experience as a student
Entry criteria for nurses: 1) Willingness to participate in the study
2) Have at least 6 months of work experience</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Exclusion criteria for nurses: 1) not wanting to participate in the study
2) His/Her work department should be changed
3) Complete the questionnaire incompletely
4) Leave more than two days by the ward nurses during the implementation of the intervention.
Exit criteria for nursing students: 1) Not willing to participate in further studies
2) Absence of more than two sessions in the internship.
3) Complete the questionnaire incompletely</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>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: During the study, the developed software will be available to the intervention groups (nurses and nursing students) (to prevent the content of the designed program from being disseminated to other students and nurses of the control group and to prevent the creation of information leakage of the software in such a way It will be designed to be installed in each mobile phone with only one password so that other people cannot use it) and they will provide their care to patients based on the developed program, and the control group will provide care to patients based on the conditions of the internship routine. will give Information will be collected using quality nursing care questionnaires and the two-part questionnaire of Kalish and Williams on a daily basis in the designed software.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Quality of nursing care. Timepoint: The beginning of the study and the end of the study. Method of measurement: Nursing care quality questionnaire.</prim_outcome>
      <prim_outcome>Missed nursing care. Timepoint: The beginning of the study and the end of the study. Method of measurement: Kalish and Williams two-part questionnaire.</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>Arak University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-06-23</approval_date>
        <contact_name>Ethics Committee of Arak University of Medical Sciences</contact_name>
        <contact_address>University complex of the great prophet,  Sardasht, Arak Arak Markazi Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
