<?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>IRCT20240610062078N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-12-21</date_registration>
      <primary_sponsor>Ghoum University of Medical Sciences</primary_sponsor>
      <public_title>impact of flipped classroom on nursing students' learning and understanding</public_title>
      <acronym></acronym>
      <scientific_title>Comparing the Effects of Flipped Classroom and Traditional Lecture Method on Academic Performance and Classroom Environment Perception among Nursing Students: A Randomized Controlled Trial</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2020-02-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/87921</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: The students were divided into two intervention and control groups using simple randomization. A Microsoft Excel random number generator with a 1:1 ratio was used to generate sequence numbers. The sequence numbers were then coded and placed in sealed opaque envelopes. The research assistant divided the students into intervention (29 people) or control (29 people) groups based on the sequence numbers in the envelope of their choice. The entire randomization process was carried out by a research assistant who was not involved in the intervention and data analysis, Blinding description: This was a single-blind study. Because this study adopted educational interventions that made it difficult to blind the participants (students) and the researcher (instructor) conducting the intervention, only the researchers responsible for data collection and analysis and for assessing the outcomes were blinded to group assignment. Thus, the researchers responsible for collecting and assessing outcomes had no access to the list of participants assigned to the intervention and control groups. The collected data were recorded and stored using random identifiers (such as unique numbers unrelated to grouping). These codes were created by the principal investigator, who had access to the decoding key. Blinded researchers collected data based on these codes and conducted outcome assessments (such as scoring tests or analyzing responses) without knowledge of the participant groupings.</study_design>
      <phase>N/A</phase>
      <hc_freetext>-.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: According to the lesson plan, the fluid and electrolytes topic was structured into four two-hour sessions delivered over four consecutive weeks. To deliver instruction using the flipped classroom approach, the instructor provided the students with all the content intended for a single session one week in advance. Students were required to review the educational materials at home or in a non-classroom setting and to arrive prepared at the subsequent session. The materials distributed included short topical videos and PowerPoint presentations (each 10–15 minutes long), along with a PDF of the lecture notes, all uploaded to the virtual educational group (Telegram). Each video and presentation concluded with a question or scenario to guide self-directed learning and evaluate students' grasp of key outcomes. Additionally, the instructor prepared questions and clinical scenarios tied to each session's core concepts prior to the class. In-Class Activities1. At the start of the class, the instructor spent 10-15 minutes addressing students' questions and clarifying misunderstandings about the educational content in order to resolve any misconceptions. 2. The instructor engaged individually with the students regarding the questions raised in the pre-class materials, which took approximately 15 minutes. 3. The students were divided into groups of five to six members to discuss the scenarios and questions prepared by the instructor. This involved the instructor presenting predesigned clinical scenarios using PowerPoint. Each group was given a few minutes to deliberate and collaborate internally in order to formulate their responses. A representative of the group presented the answer in this scenario. Members of other groups could offer comments and ask questions. Finally, the instructor addressed any remaining issues and student queries. In this way, students practically applied their theoretical knowledge by analyzing and responding to clinical scenario questions. Intervention 2: Control group: The instructor delivered educational content via a lecture using PowerPoint slides. Students’ questions were addressed at the end of the class.</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:
It can be shared after de-identifying individuals.

When:
Access begins one year after results are published.

To whom:
People working in academic and scientific institutions

Conditions:
Subject to agreement with Qom University of Medical Sciences

Where to obtain:
Faculty of Nursing, Qom University of Medical Sciences, Ms. Mahboubeh Sadat Yousefi

How to obtain:
Written and official request to the Vice President of Research, Faculty of Nursing

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mahboubeh Sadat Yousefi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Western 2nd Alley, Mo'allem St., Qom, Iran</address>
        <city>Qom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3715835155</zip>
        <telephone>+98 25 3783 1370</telephone>
        <email>mahboubeh.yousefi@yahoo.com</email>
        <affiliation>Ghoum University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mahboubeh Sadat Yousefi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Western 2nd Alley, Mo'allem St., Qom, Iran</address>
        <city>Qom</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3715835155</zip>
        <telephone>+98 25 3783 1370</telephone>
        <email>mahboubeh.yousefi@yahoo.com</email>
        <affiliation>Ghoum University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>taking the Adult and Older Adults Nursing 1 course for the first time
having access to devices such as mobile phones, computers, and the Internet for retrieving educational materials
expressing willingness to participate in the study</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Both</gender>
      <exclusion_criteria>completion of training courses related to fluid and electrolytes.
known learning disabilities
participation in a similar study at the same time</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>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: According to the lesson plan, the fluid and electrolytes topic was structured into four two-hour sessions delivered over four consecutive weeks. To deliver instruction using the flipped classroom approach, the instructor provided the students with all the content intended for a single session one week in advance. Students were required to review the educational materials at home or in a non-classroom setting and to arrive prepared at the subsequent session. The materials distributed included short topical videos and PowerPoint presentations (each 10–15 minutes long), along with a PDF of the lecture notes, all uploaded to the virtual educational group (Telegram). Each video and presentation concluded with a question or scenario to guide self-directed learning and evaluate students' grasp of key outcomes. Additionally, the instructor prepared questions and clinical scenarios tied to each session's core concepts prior to the class. In-Class Activities1. At the start of the class, the instructor spent 10-15 minutes addressing students' questions and clarifying misunderstandings about the educational content in order to resolve any misconceptions. 2. The instructor engaged individually with the students regarding the questions raised in the pre-class materials, which took approximately 15 minutes. 3. The students were divided into groups of five to six members to discuss the scenarios and questions prepared by the instructor. This involved the instructor presenting predesigned clinical scenarios using PowerPoint. Each group was given a few minutes to deliberate and collaborate internally in order to formulate their responses. A representative of the group presented the answer in this scenario. Members of other groups could offer comments and ask questions. Finally, the instructor addressed any remaining issues and student queries. In this way, students practically applied their theoretical knowledge by analyzing and responding to clinical scenario questions.</i_keyword>
      <i_keyword>Control group: The instructor delivered educational content via a lecture using PowerPoint slides. Students’ questions were addressed at the end of the class.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Academic performance. Timepoint: One week before the start of the intervention and after the end of the intervention. Method of measurement: To assess academic performance (primary outcome), pre- and post-intervention test scores were used to measure the students' knowledge gains. The tests consisted of 20 multiple-choice questions (with four options each) on knowledge related to fluid and electrolyte topics. Each correct answer was worth 1 point, with scores ranging from 0 to 20; higher scores indicated better knowledge of fluids and electrolytes.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Students' perceptions of the classroom environment (secondary outcome). Timepoint: After the end of the intervention. Method of measurement: The College and University Classroom Environment Inventory (CUCEI) was used to assess students' perceptions of the classroom environment.</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>Ghoum University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2018-07-03</approval_date>
        <contact_name>Ethics Committee of Qom University of Medical Sciences</contact_name>
        <contact_address>Shahid Lavasani (Saheli) St., Qom, I.R. Iran Qom Ghoum Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
