CClinicalTrials.gg
CompletedNCT03890874Updated Jun 5, 2019

An Analysis of the Efficacy of Different Teaching Modalities

An observational study in Simulation Training, sponsored by Jubilee Mission Medical College and Research Institute. Completed at 1 site in India. Open to participants aged 18 Years to 20 Years. Per ClinicalTrials.gov, last updated 2019-06-05.

Sponsored by Jubilee Mission Medical College and Research Institute · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 20 Years
Sex
All
01

Study summary

Didactic lectures are the currently used mode of imparting training to medical students. Use of other modes of teaching like simulation is still in its infancy. Simulation, as a teaching tool may aid in longer retention of the learning contents and also provides a safe environment for the students to practice their skills after knowledge acquisition. The aim of the study is to analyze the efficacy of different teaching modalities in imparting a particular skill, namely adult cardiopulmonary resuscitation (CPR) which is a life saving skill in first year medical students. The study population includes all the first year MBBS students and the duration of the study is 1 month. A clarity as to which mode of teaching will be ideal for memory retention is the expected outcome of this study.

Read the detailed description

Introduction

Our current medical curriculum devotes a large percentage of its time to knowledge acquisition by means of didactic lectures. Psychomotor skill acquisition takes a back seat. Certain lifesaving skills like basic life support skill training have not even made an appearance in the current curriculum. Equal time distribution to cognitive and psychomotor skills should be allotted for a subject as practical as MBBS .Simulation can prove to be a valuable tool in imparting skill training. The present study aims to evaluate the efficacy of different teaching modalities in imparting lifesaving skills in first year MBBS students.

Methods

This Cross sectional study is conducted among 33 first year students who consented to participate. Institutional ethics clearance was also obtained. The students were divided into three groups, each undergoing didactic lecture, animation based videos and simulation studies. Pretest, posttest and skills test was administered to them. One way anova, Paired t test were some of the statistical test employed using SPSS version 21.

02

Conditions studied

  • Simulation Training

Keywords

  • Cardiopulmonary Resuscitation
  • Teaching techniques
  • Basic Life Support training
  • Simulation
03

In context

Lead sponsor

Jubilee Mission Medical College and Research Institute is the lead sponsor of 25 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 20 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

First year Medical students of Jubilee Mission Medical college and Research Institute.

Inclusion criteria

  • All First year MBBS Students who are willing to participate

Exclusion criteria

Exclusion Criteria:

  • Prior training in adult CPR skills
  • Physical disabilities that does not permit performing high quality CPR
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • First year medical students

    First year medical students of jubilee mission medical college and research institute

06

What researchers measure

Primary outcomes

  1. comparing the mean post test score of groups of students that underwent training using different teaching modalities assessed using a ten part multiple choice questionnaire.

    Amongst visual, didactic and simulation models of teaching, to identify the more effective strategy to impart Basic Life Support (BLS) knowledge to first year medical students through a four hour training programme, by comparing the mean post test scores of each group

    Time frame: 4 hours

Secondary outcomes

  1. comparing the change in the baseline test score amongst first year medical students taught by visual, didactic and simulation models.

    students through a four hour training programme, by comparing the mean pre test and post test scores of each group

    Time frame: 4 hours

  2. comparing the mean score of groups of students that underwent training using different teaching modalities, assessed by an examiner testing their skills using a pre set basic life support checklist proforma.

    comparing the effectiveness of each teaching modality amongst first year medical students to impart Adult Cardiopulmonary Resuscitation (CPR) skills assessed by an examiner observing and testing their skills using a pre set checklist proforma.

    Time frame: 4 hours

07

Study locations

1 site
  • Jubilee mission medical college and research institute
    Thrissur, Kerala 680005, India
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 5, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03890874
Lead sponsor
Jubilee Mission Medical College and Research Institute
Responsible party
Appu Suseel (Assistant Professor, Jubilee Mission Medical College and Research Institute) — Principal investigator
First posted
Mar 26, 2019
Start date
Mar 17, 2019
Primary completion
Apr 25, 2019
Completion
Apr 30, 2019
Last update
Jun 5, 2019

Study contacts

Pallavi Panchu, MD
study chair · Jubilee Mission Medical College and Research Institute

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion