<?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>IRCT20200928048865N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-01-01</date_registration>
      <primary_sponsor>The University of Mashhad Medical Science</primary_sponsor>
      <public_title>The effect of environmental health education on self-efficacy and anxiety caused of Covid-19</public_title>
      <acronym></acronym>
      <scientific_title>The effect of environmental health education program on efficacy and anxiety of covid-19 among nurses</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2020-11-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/51258</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The sampling method (inclusion of nurses in the study) in this study will be non-randomly targeted; Thus, considering that out of 10 different wards of Shahid Kamyab hospital, Surgical Wards 1 and ICU2 are the only wards from where patients are referred to other wards; So these two sections will be selected. Surgery 1 has 45 nurses and ICU2 has 36 nurses.
Assignment of nurses to intervention and control groups will be done randomly. In this way, each of the nurses in Surgery 1 will be assigned a two-digit code (1-45) and then using a table of random numbers and selection of two-digit numbers, the nurses will be allocated as every other one to intervention and control groups. Obviously, in a table of random numbers, if we come across numbers greater than 45 or 00, we will skip it. This will continue until 15 people are selected for each of the two intervention and control groups. The same will be done for ICU2. Finally, 15 people will be selected from each section for each group (and a total of 30 people in each group).</study_design>
      <phase>N/A</phase>
      <hc_freetext>The effect of environmental health education program on efficacy and anxiety of covid-19 among nurses.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: For the intervention group, 3 60-minute combined sessions will be held in person and virtually (webinar). A face-to-face meeting with health tips and social distance is held in the form of lectures - group discussions, questions and answers, slide shows. Content of environmental health trainings, including: Hand hygiene, standard precautions (infection control, environmental pollution control, surface disinfectants (types, application and important points in preventing coronavirus)). Data collection tools including demographic information form, Scherer standard self-efficacy questionnaire and standard coronary anxiety questionnaire (CDAS) will be completed by the intervention and control group at the beginning of the session.Then the other two sessions are held as a webinar (virtual) for the intervention group. Immediately after the end of the training program and one month later, in both intervention and control groups, standard questionnaires, self-efficacy (Scherer) and Covid-19 anxiety (CDAS) in both psychological and physical dimensions will be completed and evaluated. Intervention 2: Control group: They receive the usual training of the medical center. Training contents for the intervention group will be provided to the control group after intervention.</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:
Data on coronary anxiety and self-efficacy in nurses can be shared.

When:
After publishing the article and defending the dissertation

To whom:
Project partners

Conditions:
People who do similar research

Where to obtain:
It will be done by email with the person in charge of the project.

How to obtain:
Data is made available to individuals via email.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Zahra Emami Moghadam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Chaharrah Doktora- Nursing University</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9137913199</zip>
        <telephone>+98 51 3802 6310</telephone>
        <email>Emamiz@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Zahra Emami Moghadam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Chaharrah Doktora- Nursing University</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9137913199</zip>
        <telephone>+98 51 3802 6310</telephone>
        <email>emamiz@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Have a bachelor's or master's degree in nursing
Working in the medical department of the hospital
Not participating in a study similar to the present study</inclusion_criteria>
      <agemin>24 years</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Reluctance to participate in research
Having a chronic illness
Participate in similar research over the past two months
Diagnosed with mental disorder</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: For the intervention group, 3 60-minute combined sessions will be held in person and virtually (webinar). A face-to-face meeting with health tips and social distance is held in the form of lectures - group discussions, questions and answers, slide shows. Content of environmental health trainings, including: Hand hygiene, standard precautions (infection control, environmental pollution control, surface disinfectants (types, application and important points in preventing coronavirus)). Data collection tools including demographic information form, Scherer standard self-efficacy questionnaire and standard coronary anxiety questionnaire (CDAS) will be completed by the intervention and control group at the beginning of the session.Then the other two sessions are held as a webinar (virtual) for the intervention group. Immediately after the end of the training program and one month later, in both intervention and control groups, standard questionnaires, self-efficacy (Scherer) and Covid-19 anxiety (CDAS) in both psychological and physical dimensions will be completed and evaluated.</i_keyword>
      <i_keyword>Control group: They receive the usual training of the medical center. Training contents for the intervention group will be provided to the control group after intervention.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Self-efficacy. Timepoint: "At the beginning of the study (before the intervention) and immediately after the intervention, one month after the end of the study". Method of measurement: Data collection tools including demographic information form, Scherer standard self-efficacy questionnaire are used to measure nurses' self-efficacy.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Coronary Anxiety Disorder (CDAS). Timepoint: "At the beginning of the study (before the intervention) and immediately after the intervention, one month after the end of the study". Method of measurement: standard questionnaire of anxiety caused by Quid-19 in both psychological and physical dimensions are used in nurses.</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>The University of Mashhad Medical Science</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2020-09-29</approval_date>
        <contact_name>IR.MUMS.NURSE.REC</contact_name>
        <contact_address>School of Nursing and Midwifery, Ph.D. Intersection, Ibn Sina St.University St. Mashhad Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
