<?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>IRCT20130718014049N11</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-01-07</date_registration>
      <primary_sponsor>Jahrom University of Medical Sciences</primary_sponsor>
      <public_title>The effect of aromatherapy with lavender oil and Citrus Limon on undergraduate students anxiety before the post-internship Objective Structured Clinical Examination test (OSCE)</public_title>
      <acronym></acronym>
      <scientific_title>The effect of aromatherapy with lavender oil and citrus limon on undergraduate students of the faculty of nursing and para-medicine anxiety before the post-internship Objective Structured Clinical Examination test (OSCE)</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2023-12-31</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>80</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/67399</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Triple blinded, Placebo: Used, Assignment: Parallel, Purpose: Supportive, Randomization description: The division will be random allocation based on the class list in such a way that the students number 1, 2 and 3 of the list of each class will be divided into the intervention group with lavender and the intervention group with citrus lemon and control, by throwing a dice and randomly. The rest of the students will be systematically divided into the above groups. Numbers 1 and 4 of the dice will be assigned to the intervention group with lavender, numbers 2 and 5 of the dice will be assigned to the intervention group with citrus lemon, and numbers 3 and 6 of the dice will be assigned to the control group.
This process will be done for all groups, Blinding description: This is a triple-blind study, the nature of the essential oil is unknown to the study participant, Outcome assessor, and the data analyst.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Anxiety of undergraduate students before the Objective Structured Clinical Examination (OSCE) test at the end of the course.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of lavender essential oil will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students. Intervention 2: Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of Citrus Limon L will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students. Intervention 3: Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of distilled water will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students.</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:
IPD collected for the primary outcome measure only

When:
Six months after printing results

To whom:
Only available for people working in academic institutions

Conditions:
Only scientific and practical use is allowed

Where to obtain:
Jahrom University of Medical Sciences

How to obtain:
Apply to university and receive information

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ali Abbasi jahromi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Ostad Motahari Blvd, Jahrom University of Medical Sciences</address>
        <city>Jahrom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7414846199</zip>
        <telephone>+98 71 5434 0406</telephone>
        <email>aliabbasijahromi@yahoo.com</email>
        <affiliation>Jahrom University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Ali Abbasi jahromi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Ostad Motaharie Blvd, Jahrom University of Medical Sciences</address>
        <city>Jahrom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7414846199</zip>
        <telephone>+98 71 5434 0406</telephone>
        <email>aliabbasijahromi@yahoo.com</email>
        <affiliation>Jahrom University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>All final year undergraduate students of nursing and paramedical faculties
Consent to participate in the study</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>25 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having a respiratory sensitivity to the scent of lavender and citrus limon
Having olfactory disorders
Use of sedative drugs
Using stress-reducing methods such as music therapy and...
Having anxiety disorders</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>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Placebo</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of lavender essential oil will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students.</i_keyword>
      <i_keyword>Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of Citrus Limon L will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students.</i_keyword>
      <i_keyword>Intervention group:At the beginning of the research, the students' demographic information questionnaire will be filled and for the first time, Sarason's anxiety and vital signs questionnaire will be completed by each student. Then, the intervention group will be placed in a classroom that has been completely cleaned and properly ventilated. A tissue paper with 3 drops of distilled water will be placed on each chair. The distance between these tissue papers and the nose of the participants will be 15 cm. 15 minutes after the placement of the students in the class, the Sarason and vital signs questionnaire will be completed again by the students, and finally, for the third time and after the test, the Sarason and vital signs questionnaire will be completed by each student after the test. Vital signs will be measured by Saadat model vital signs monitor and will be announced to the students.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Test anxiety score. Timepoint: Before the intervention, 15 minutes after the intervention, after the test. Method of measurement: Sarason 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>Jahrom University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-12-16</approval_date>
        <contact_name>Ethics committee of Jahrom University of Medical Sciences</contact_name>
        <contact_address>Ostad motahhary Blvd, Jahrom University of Medical Sciences Jahrom Fars Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
