Comparison of Learning in Traditional Versus "Flipped" Classrooms

January 27, 2020 updated by: Children's Hospital of Philadelphia

Comparison of a "Flipped" Classroom Methodology to Traditional Instructional Techniques for Neonatal-perinatal Medicine Fellows: A National Prospective Study

This is an educational research study to compare knowledge retention of neonatal-perinatal medicine (NPM) fellowship trainees instructed on a subsection of the American Board of Pediatrics (ABP) NPM Content Outline using traditional didactic lectures (control group) versus a flipped classroom methodology (intervention group). The primary objectives are to assess whether the flipped classroom provides equivalent or superior outcomes for knowledge acquisition and retention compared to traditional lecture-based formats, based upon baseline and serial knowledge assessments (after the educational session, and at 3- and 6- month intervals). The secondary outcomes are learner and educator preference.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Sixty-three ACGME-accredited NPM fellowship training programs in the United States have enrolled to participate in this study. Programs have been randomized to teach a subsection of neonatal physiology using the traditional didactic approach or using the "flipped" classroom methodology.

The ACGME requires that NPM fellowship programs provide formal instruction to teach trainees about key concepts in the care of neonates and infants, and most programs have traditionally utilized didactic presentations to relay this information. These sessions are typically instructor-centered, with little requirement for involvement or engagement on the part of the learner, and are not felt to optimize long-term knowledge acquisition and retention. A newer educational model, the "flipped" classroom, increases the opportunities for learner engagement and requires investment and preparation. Using this educational structure, fellows receive learning materials that need to be reviewed prior to the in-person educational session. The participants will then spend the in-person session actively engaged in applying the knowledge to answer questions, participate in discussions, and solve problems. Adult learning theory supports this active involvement as a way to increase learner engagement, improve recognition of meaning of the material, and improve knowledge acquisition and long-term retention.

Fellowship Program Directors involved in the Organization of Neonatal Training Program Directors (ONTPD) have been contacted about the opportunity to participate in this prospective multi-center study. After enrollment, program directors will complete a brief survey of their program's baseline educational methods and demographics. Fellows will be contacted directly by local site PIs for individual consent to data collection. Fellows will be asked to provide demographic information, assessment of learning style/ practices, time devoted to educational pursuits, and perceptions of current physiology education. The fellows will be asked to complete 4 knowledge assessments (baseline, at the end of the educational block, 3 months, 6 months) in REDCap over the course of 6 months. All data will be de-identified, and individual and programmatic data will be anonymous. The assigned ABP content will be taught within the same 3-month period any time between September 2018 and March 2019 via the assigned method (traditional didactic or flipped classroom). All educational materials will be provided to both arms of the study. Learning objectives will be based on the ABP NPM Content Outline and materials with be authored by experts in neonatal physiology. Materials will undergo rigorous peer-review by an editorial board. Traditional/control fellows will be instructed using the provided educational materials in an instructor-led didactic slide presentation. Intervention group fellows will be required to view the same educational materials in online videos prior to their assigned classroom session. During the "flipped" classroom session, the fellows will work through a series of questions based on the assigned educational materials with a local facilitator using a facilitation guide who has been trained in flipped classroom facilitation. This facilitator guide will present discussion points based upon the pre-learning materials and requires learners to apply acquired knowledge. The facilitator guides are also peer-reviewed for content and quality.

In the present study, only the ABP Content Objectives for NPM on gastroenterology and bilirubin will be included. Educational materials will be reviewed and revised by a 4-member editorial board to ensure accuracy, completeness, and quality. For online viewing, these materials are uploaded on MedEdOnTheGo.com, an online learning management platform. Fellows will be provided with additional reading materials, such as seminal articles or textbook chapters, that will allow them to develop a deep understanding of the topic.

Fellows will be surveyed regarding their learning experiences at 3 different time points; before the educational intervention begins, at the completion of the educational intervention, and 3 months after completion of the intervention. Fellows will complete anonymous surveys in REDCap regarding their learning experiences, class preparation, the quality of teaching, perceived effectiveness of teaching efforts, and preferences for learning. Fellows will also participate in short 15-item multiple choice quizzes to measure knowledge retention. There will be 4 quizzes in total; prior to the intervention (baseline), at the completion of the intervention, 3 months post, and 6 months post-intervention. These quizzes will be proctored and closed book. Fellows in either randomization arm will answer the same questions. The quiz questions will cover the specific content addressed in the educational sessions, be created by the study team, and piloted by attending neonatologists for clarity, accuracy, and relevance.

Data will be tabulated on baseline information for both program level and fellow level with testing to determine if pre-intervention testing data is different between groups (equivalence variance 2-tailed T-tests for continuous data and likert scores, and chi square for categorical data). Knowledge retention curves will be developed by performing T-tests of mean scores for each time point. Post-education surveys for program directors and fellows will be evaluated to assess effect of interventions using equal variance 2-tailed T-tests for continuous data and likert scores.

Study Type

Interventional

Enrollment (Actual)

538

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19104
        • The Children's Hospital of Philadelphia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Fellow or educator in an ACGME-accredited Neonatal-Perinatal Medicine Fellowship program in the US.

Exclusion Criteria:

  • Not a fellow or educator in an ACGME-accredited Neonatal-Perinatal Medicine Fellowship program in the US.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Traditional Didactic Education
Education will be provided to fellows using the traditional didactic approach (lecture-based).
Experimental: Flipped Classroom Education
Education will be provided to fellows using the flipped classroom approach.
Fellows will receive GI/Bilirubin education in a flipped classroom format.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge retention
Time Frame: 9 months
Knowledge retention will be tested using multiple choice examinations.
9 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Learner Preferences
Time Frame: 6 months
Learner preferences for how to receive education will be assessed through qualitative survey
6 months
Educator Preferences
Time Frame: 6 months
Educator preferences for how to provide education will be assessed through qualitative survey
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2018

Primary Completion (Actual)

September 30, 2019

Study Completion (Actual)

September 30, 2019

Study Registration Dates

First Submitted

November 19, 2018

First Submitted That Met QC Criteria

November 28, 2018

First Posted (Actual)

November 29, 2018

Study Record Updates

Last Update Posted (Actual)

January 28, 2020

Last Update Submitted That Met QC Criteria

January 27, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 18-015235

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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