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AuscultationNCT06359158

Enhancing Respiratory Auscultation Skills Among Medical Students: Digital Stethoscopes in Medical Education

A study testing Digital stethoscope use in people with Auscultation and Breathing Sound, run by Chung Shan Medical University at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Objectives: This study aims to assess the effectiveness of a novel digital stethoscope curriculum integrated into respiratory auscultation training for medical students. It seeks to compare the auscultation proficiency gained through this innovative approach with that from traditional teaching methods, to understand… Read more about this study

Who is it for?
Ages 21 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Auscultation, Breathing Sound, Asthma
What is being tested?
Digital stethoscope use
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
84 participants
Where
1 siteTaiwan
Study dates
1 Aug 2023to 31 Jan 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Medical students who were completing their clinical clerkship rotations in the Department of Thoracic Surgery during the study period.

Who cannot join

  • All medical students who did not complete the clinical clerkship rotations, the pre- and post-tests, and the course feedback questionnaire.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Chung Shan Medical University Hospital

    Taichung, South, 402

Other trials in Taiwan

About this study

Official title: Enhancing Respiratory Auscultation Skills Among Medical Students: A Randomized Controlled Trial on the Integration of Digital Stethoscopes in Medical Education

Objectives: This study aims to assess the effectiveness of a novel digital stethoscope curriculum integrated into respiratory auscultation training for medical students. It seeks to compare the auscultation proficiency gained through this innovative approach with that from traditional teaching methods, to understand the potential of digital stethoscopes in reinvigorating clinical skills training.

Methods: In a single-center, controlled, longitudinal, randomized experimental design, 84 medical students undergoing clinical clerkship rotations at Chung Shan Medical University Hospital were enrolled. Participants were randomly assigned to either the intervention group, receiving training with digital stethoscopes and the Eko auscultation software, or the control group, following a traditional curriculum. Pre- and post-intervention assessments measured auscultation skills, and student feedback on teaching quality was collected. The primary outcome was the improvement in auscultation proficiency, while secondary outcomes included student engagement and feedback on the educational approach.

Expected Results: The investigators hypothesize that the integration of digital stethoscopes into the curriculum will significantly improve the auscultation skills of medical students compared to traditional methods. Enhanced engagement and positive feedback from students are anticipated, underscoring the pedagogical value of incorporating digital health technologies in medical education.

Read the detailed description

Subjects and Procedures Research Methodology The present investigation carried out at a university hospital, was a longitudinal, controlled, single-center, randomized trial with an interventional design. A total of 84 medical students who were completing their clinical clerkship rotations in the Department of Thoracic Surgery were included in the study. The participants were randomized to either the intervention group or the control group.

Intervention The participants in the intervention group were provided with the curriculum titled "Respiratory Auscultation with Digital Stethoscopes," which involved the use of electronic digital stethoscopes and the Eko auscultation software platform developed by Eko Devices in Berkeley, California, USA. The utilization of this methodology enabled the viewing and examination of documented respiratory sounds, which were then shown as phonopneumograms. The participants assigned to the control group were provided with conventional respiratory auscultation training in accordance with the established clerkship curriculum. The curriculum encompassed practical sessions conducted at the Objective Structured Clinical Examination (OSCE) center, utilizing the SAM II respiratory sound simulator (Cardionics, Webster, Texas, USA). Additionally, instructional videos were provided to facilitate the acquisition of knowledge pertaining to breath sounds. Furthermore, a breathing assignment was assigned to each student, necessitating the recording and description of five distinct breath sounds. The process of gathering data The Zuvio Interactive Response System (Zuvio, Taipei, Taiwan) was used to measure participants' auscultation skills before and after the intervention. This was done by employing a question bank consisting of 50 breath sound audio files. The collection of student feedback regarding the quality of teaching and the helpfulness of the course was conducted by means of surveys employing 5-point Likert scales. Furthermore, the researchers collected data pertaining to OSCE attendance, video viewing, answer-checking behavior, and the time interval between pre-and post-tests. The variables that were assessed included alterations in auscultation test scores and self-reported levels of teaching satisfaction within the two cohorts.

Statistical analysis The data analysis was performed utilizing the Statistical Package for Social Sciences (IBM SPSS Statistics, version 25). A range of statistical tests were employed to comprehensively analyze the distribution of student scores and teaching satisfaction, compare the intervention and control groups, and explore the influence of the course on students' engagement and learning outcomes. The normality of distributions for student scores and teaching satisfaction was initially examined using the Kolmogorov-Smirnov test. To compare scores and satisfaction levels between the intervention and control groups, either the Student t-test or the Mann-Whitney U test was selected, depending on the distributions. The paired Student's t-test or the Wilcoxon signed-rank test was used, as appropriate, to assess the changes in scores before and after the course. The study employed the chi-square test to examine the disparity in the proportions of students from both groups who opted to rent electronic stethoscopes subsequent to the completed course. This was conducted as an indirect method to assess the student's level of interest in auscultation and their comprehension of digital stethoscope technology, hence indicating the effectiveness of the course instruction. In addition, the researchers used regression analysis to investigate the relationships between different variables and outcomes, thereby offering valuable insights into the determinants that impact students' learning experiences and preferences. The statistical significance level was set at p<0.05.

Being tested
Digital stethoscope use
Keywords
Medical Education, Auscultation Pedagogy, Digital Stethoscope, Clinical Skills Training
Medical subject headings
Respiratory Sounds, Asthma, Pneumonia, Pleural Effusion

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Digital stethoscope useDevice

    Also called video, Pre- and Post- test, Questionnaire on student feedback

    In this interventional study, 84 medical students were randomly allocated to an intervention group utilizing a novel digital stethoscope curriculum or a control group receiving traditional instruction. The intervention leveraged digital stethoscopes, enabling visualization and analysis of recorded breath sounds. Pre- and post-assessments evaluated respiratory

Study groups in NCT06359158
Study groupRoleWhat they receive
Digital stethoscope useExperimentalThe intervention comprises a comprehensive curriculum titled "Respiratory Auscultation with Digital Stethoscopes," designed to enhance the proficiency of medical students in diagnosing respiratory disorders through auscultation. The curriculum utilizes advanced digital stethoscope technology, specifically electronic digital stethoscopes, and the Eko auscultation software platform, to facilitate the visualization and analysis of recorded breath sounds, thereby augmenting traditional auscultation training methods.
Receives: Device: Digital stethoscope use
Traditional stethoscope useNo interventionThe curriculum utilizes a traditional stethoscope.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pre-test and Post-test using the Zuvio Interactive Response System (Zuvio, Taipei, Taiwan)

    The Zuvio Interactive Response System evaluates participants' auscultation skills through a question bank of 50 breath sound audio files.

    Measured: At the beginning and end of the two-week Thoracic Surgery clinical rotation.

  2. Student Feedback

    Helpfulness of the course: Student feedback on teaching quality and course helpfulness was collected through surveys using 5-point Likert scales.

    Measured: End of the two-week Thoracic Surgery clinical rotation.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Apr 2024
  2. Study start1 Aug 2023
  3. Primary completion31 Jan 2024
  4. Study completion31 Jan 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
84 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06359158
Sponsor's protocol ID
eStethoscope for Med Student
Status last verified
Apr 2024
First submitted
23 Mar 2024
Last updated
11 Apr 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Digital stethoscope use in people with Auscultation and Breathing Sound, run by Chung Shan Medical University at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pre-test and Post-test using the Zuvio Interactive Response System (Zuvio, Taipei, Taiwan) (time frame: At the beginning and end of the two-week Thoracic Surgery clinical rotation.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2024.

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