SimAG: HFS in the Assessement and Management of Severe Asthma Attack Among Fifth Year Medical School Students

Sponsor
University of Monastir (Other)
Overall Status
Completed
CT.gov ID
NCT02776358
Collaborator
(none)
33
1
2
8
4.2

Study Details

Study Description

Brief Summary

Bedside clinical case learning, such for respiratory distress, represent a challenge for medical teachers, especially in critical conditions. In fact, this kind of learning implicate the presence of an appropriate case (the patient itself), framework and may be time consuming which could compromise the patient's safety and wellbeing.

New pedagogic tools have emerged to strengthen the medical reasoning and the acquisition of knowledge. in recent years, the development of medical simulation has found a growing interest in the medical teaching field. Contextualization, reproducibility and reliability are the characteristics of high-fidelity simulation (HFS) which guarantee a lifetime experience of clinical conditions without putting at risk patient's safety and comfort.

The aim of this study is to assess the impact of HFS on fifth year medical students learning skills in the assessement and management of an acute asthma attack in the emergency room, and to compares it to other modern teaching tools such as "video-case"

Condition or Disease Intervention/Treatment Phase
  • Other: High Fidelity Simulation
  • Other: Video case
Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
High Fidelity Simulation (HFS) Versus Video-case(VC) Trainings in the Assessement and Management of Severe Asthma Attack Among Medical School Students: a Randomized Controlled Study
Study Start Date :
Sep 1, 2014
Actual Primary Completion Date :
May 1, 2015
Actual Study Completion Date :
May 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: High Fidelity Simulation

Students will receive a 1 hour High fidelity simulation session

Other: High Fidelity Simulation
A HFS session for an asthma attack require: a 5 minutes briefing session: case and equipments presentation and choice of participants 15 minutes of actual simulation 40 minutes of debriefing A pre and a post test will be taken by the students before and after the session and a satisfaction questionnaire at the end of the course. Also, another test will be done after 7 days of the course.

Experimental: Video Case

Students will receive a 1 hour assisted Video Case learning session

Other: Video case
a video case (or video box) session in which students will attend a video-projection of a real case of an asthma attack and discuss with the trainer the different steps of the assessement and management of an asthma attack. A pre and a post test will be taken by the students before and after the session and a satisfaction questionnaire at the end of the course. Also, another test will be done after 7 days of the course.

Outcome Measures

Primary Outcome Measures

  1. Difference between the pre and the post-test scores in each group (delta Score) [Just before the teaching course (baseline) and one hour later]

    The difference between the pre and the post-test scores is calculated as follow: delta score = post-test score - pre-test score

Secondary Outcome Measures

  1. Late performance score [7 days after the teaching course]

    This score is calculated based on a test taken 7 days after the teaching course to assess the students memory of the clinical case and acquired knowledge.

  2. Level of satisfaction [one hour after the teaching course]

    A five point likert scale is given to each student to assess their level of satisfaction regarding the teaching technique.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • all fifth year medical students allocated to the one month internship period in the emergency departement.
Exclusion Criteria:
  • students refusing to participate in the protocol.

Contacts and Locations

Locations

Site City State Country Postal Code
1 university of Monastir Monastir Tunisia 5000

Sponsors and Collaborators

  • University of Monastir

Investigators

  • Principal Investigator: Mohamed habib Grissa, MD, Emergency Department , university hospital of Monastir, TUNISIA
  • Principal Investigator: Nouira Semir, Professor, Emergency Department , university hospital of Monastir, TUNISIA

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pr. Semir Nouira, Clinical Professor, University of Monastir
ClinicalTrials.gov Identifier:
NCT02776358
Other Study ID Numbers:
  • SimAG
First Posted:
May 18, 2016
Last Update Posted:
May 18, 2016
Last Verified:
May 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 18, 2016