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CompletedNCT01596465Updated Jun 2, 2021

Study of Two Teaching Techniques to Teach Cardiac Auscultation to Physicians

An interventional study of Self-Study using MP3 Player and Multimedia Lecture in Heart Murmur, sponsored by The Reading Hospital and Medical Center. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2021-06-02.

Sponsored by The Reading Hospital and Medical Center · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
83
Allocation
Randomized
Sex
All
01

Study summary

Our objective was to test two educational interventions for teaching cardiac auscultation: self-directed learning using portable audio files versus a single, massed multimedia lecture intervention similar to current best practice, to determine which would most effectively increase recognition of common cardiac sounds by physicians. The investigators hypothesized that doctors learning on their own time could better improve their skills.

Read the detailed description

Participants All non-cardiologist physicians were eligible for the study and responded to recruitment advertising. Participants were 83 non-cardiologist physician volunteers (57 practicing physicians, 26 residents in training) from one Academic Independent Medical Center in the Northeastern United States enrolled between January 11, 2011 and February 25, 2011. Participants were randomized by study investigators using a table of random numbers. All participants were given an MP3 player at the time of enrollment for compensation of their time, but received no grade for participation. Participants provided their informed consent before enrolling in the study.

Educational Interventions Following the pretest, participants in the interventional arm of the study were given an MP3 player which contained eight, 15-second heart sound files (7 pathologic heart sound files and 1 normal heart sound file) alternated with nine leisure songs. MP3 players could play files in order or "shuffle" files in random order. Each heart sound file was introduced by the narrated phrase "Identify this sound,", followed by 10 beats of a heart sound recording, then the narrated identification of the heart sound. Participants were asked to use the MP3 player in order to improve their auscultation skills as often as they could and asked to record their activities while listening, but were given no further training.

Following the pretest, participants in the control arm received a 1-hour multimedia lecture (Power Point) taught by the same faculty member (AGK), which reviewed the pathophysiology, exacerbating and relieving factors, as well as visual diagrams of the heart sounds. The normal and seven pathologic heart sounds were played for participants during the lecture for a total of 2 minutes through high-quality home stereo speakers, exposing learners to 1280 beats in the 1-hour session. Abnormal sounds were taught in groups of systolic, diastolic and extra sounds, and were first introduced by name, and then as unknowns using mixed practice in each of the three sections. At the end of the session, control group participants were given an MP3 player with no heart sound files as honoraria. Both the intervention and control group were told they would be retested at 12 weeks. Both were given a paper copy of the Power Point slides for self-study, but had no electronic access to the original slides. Both groups were asked not to discuss the study with the other participants.

Content of the audio files The audio files of the heart sounds were obtained from actual patients and have validity evidence generated in prior studies. The pathologic sounds included aortic stenosis, aortic insufficiency, mitral stenosis, mitral insufficiency, mitral valve prolapse, S3, S4, and the normal heart sound. These heart sounds collectively represent the most important auscultatory findings according to a previously published national survey of residency program directors.

Measurement All participants took a 15-question pretest in addition to a posttest at 12 weeks using identical heart sound files to those used in training. Tests consisted of 8-second clips of each heart sound file, with 10 beats of each sound. Participants were given 15 seconds after each question to choose the correct response from an extended match list that included 9 choices, one of which was not represented among the training materials ("benign flow murmur"). Each of the 7 pathologic heart sounds were represented twice, with normal heart sounds represented once. The order of questions for the test was randomly selected. The same speakers used in the lecture format were also employed utilized for testing. Study examiners tested the speaker sound quality before each test. All tests were independently hand-graded by two graders, and all discrepancies in handwriting and scoring were resolved by consensus of both investigators. Grades were not shared with participants.

Both groups were asked to rate their prior experience with pathologic heart sounds, including observation and feedback they have received, satisfaction with the teaching modality and confidence in their auscultatory skill at the pretest and posttesting. Both groups audited their preference for learning style by the VARK© learning style assessment instrument Version 7.0, at the time of enrollment. Both groups were asked to record any other methods used to study auscultation during the study period. Intervention group exposure to heart sounds was determined by electronic interrogation of their MP3 player at 12 weeks. Play counts recorded by the device were reviewed by both study investigators and entered on an electronic spreadsheet.

Data analysis Demographic comparisons, Likert scales of satisfaction and pathologic heart sound exposure between control and intervention groups were performed via Chi-square testing and Student's t-test as appropriate. Internal consistency of the pretest was performed using Cronbach's alpha. Total study time was recorded as 60 minutes for the control group, and was calculated by the total number of recorded plays multiplied by 15 seconds per play for the intervention group. Additional self-reported study methods and amount of exposure were recorded but not added to control and intervention study time calculations. The primary outcome was the difference in test score from pretest to posttest and was compared using paired t-tests. Effect sizes for both arms were computed using differences in means divided by pooled standard deviations. Correlations between exposure and improvement from pretest to posttest in the intervention group were calculated by linear regression. Subgroup analysis of intervention group participants who did not use their MP3 player between weeks 4 and 12 (defined as play count= 0 during time interval) was performed to approximate decay in that group, and was analyzed by paired t-test. The auditory learning preference of the VARK learning style inventory was characterized dichotomously as present or absent. A two-factor ANOVA was performed comparing intervention and control groups with presence of auditory learning style against the primary outcome as the dependent variable to determine the relative effects of learning style and instructional method. Power calculations were made for the observed differences between the control and intervention arms for both variables of the primary objectives.

02

Conditions studied

  • Heart Murmur

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03

In context

Heart Murmurs

46 studies on the registry are indexed under Heart Murmurs; 6 are open to participants now.

This study's enrollment of 83 is close to the median of 92 across 26 interventional studies indexed under Heart Murmurs.

Browse Heart Murmurs studies →

Lead sponsor

The Reading Hospital and Medical Center is the lead sponsor of 9 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All non-cardiologist physicians from one institution were eligible for the study. Participants were 83 non-cardiologist physician volunteers (57 practicing physicians, 26 residents in training) from one Academic Independent Medical Center in the Northeastern United States enrolled between January 11, 2011 and February 25, 2011.

Exclusion criteria

Exclusion Criteria:

  • Cardiologists,
  • Non-physicians.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
83 participants (actual)

Study arms

  • Active comparator
    Control

    Control arm

    Other: Multimedia Lecture

  • Active comparator
    Intervention

    Intervention arm

    Other: Self-Study using MP3 Player

Interventions

  • OtherSelf-Study using MP3 Player

    Participants in the interventional arm of the study were given an MP3 player which contained eight, 15-second heart sound files (7 pathologic heart sound files and 1 normal heart sound file) alternated with nine leisure songs. MP3 players could play files in order or "shuffle" files in random order. Each heart sound file was introduced by the narrated phrase "Identify this sound,", followed by 10 beats of a heart sound recording, then the narrated identification of the heart sound. Participants were asked to use the MP3 player in order to improve their auscultation skills as often as they could and asked to record their activities while listening, but were given no further training.

    Also known as: Self-Study

  • OtherMultimedia Lecture

    Following the pretest, participants in the control arm received a 1-hour multimedia lecture (Power Point) taught by the same faculty member (AGK), which reviewed the pathophysiology, exacerbating and relieving factors, as well as visual diagrams of the heart sounds. The normal and seven pathologic heart sounds were played for participants during the lecture for a total of 2 minutes through high-quality home stereo speakers, exposing learners to 1280 beats in the 1-hour session. Abnormal sounds were taught in groups of systolic, diastolic and extra sounds, and were first introduced by name, and then as unknowns using mixed practice in each of the three sections.

    Also known as: Lecture

06

What researchers measure

Primary outcomes

  1. Improvement in auscultation score at 4 and 12 weeks

    Primary outcome was an improvement in test score from pre-test to 4 and 12-week post-test. All participants took a 15-question pretest in addition to a posttest at 4 and 12 weeks using identical heart sound files to those used in training. Each test Tests consisted of 8-second clips of each heart sound file, with 10 beats of each sound.

    Time frame: 12 weeks

Secondary outcomes

  1. Learner Satisfaction

    Both groups were asked to rate satisfaction with the teaching modality at the pretest and posttesting via 6-point Likert scale.

    Time frame: 12 weeks

  2. Learner confidence

    Both groups were asked to rate confidence in their auscultatory skill at the pretest and posttesting at 12 weeks on a 6-point Likert scale.

    Time frame: 12 weeks

07

Study locations

1 site
  • The Reading Hospital and Medical Center
    West Reading, Pennsylvania 19612, United States
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2011, a primary completion of Jun 2011 and a completion of Oct 2012. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
May 8, 2012
First posted
May 11, 2012
Start
Jan 2011
Primary completionActual
Jun 2011
CompletionActual
Oct 9, 2012
Last update
Jun 2, 2021
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 2, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01596465
Lead sponsor
The Reading Hospital and Medical Center
Responsible party
Anthony A. Donato (Associate Program Director, Internal Medicine, Reading Hospital and Medical Center; Clinical Associate Professor, Internal Medicine, Jefferson Medical College, The Reading Hospital and Medical Center) — Principal investigator
First posted
May 11, 2012
Start date
Jan 2011
Primary completion
Jun 2011
Completion
Oct 9, 2012
Last update
Jun 2, 2021

Study contacts

Anthony A Donato, MD
study director · The Reading Hospital and Medical Center
Antony G Kaliyadan, MD
principal investigator · The Reading Hospital and Medical Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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