Comparative Evaluation of Ultrasound-Guided Femoral Nerve Block Training With Low-Fidelity Low-Cost Simulation Model Among Junior Doctors in Department of Emergency Medicine USM.

May 16, 2026 updated by: AHMAD AFIQ BIN ABDULLAH ZAN, Universiti Sains Malaysia

Comparative Evaluation of Ultrasound-Guided Femoral Nerve Block Training With Low-Fidelity Low-Cost Simulation Model Among Junior Doctors in Department of Emergency Medicine USM

To study the effectiveness of low-fidelity ultrasound-guided femoral nerve block training interventions score in knowledge and skills performance among junior doctors in the Department of Emergency Medicine Universiti Sains Malaysia, with the aim of assessing its mean.

Study Overview

Detailed Description

1. To compare the mean score of knowledge of junior doctors in performing ultrasound-guided femoral nerve block in the emergency department pre and post training simulation.

2. To compare the mean score of skills of junior doctors in performing ultrasound-guided femoral nerve block in the emergency department pre and post training simulation.

3. To determine the impact of the low-fidelity, low-cost bovine meat-based simulation model for ultrasound-guided femoral nerve block training on confidence among junior doctors working in the emergency department

Study Type

Interventional

Enrollment (Estimated)

36

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

    • Kelantan
      • Kubang Kerian, Kelantan, Malaysia, 16150
        • Hospital Universiti Sains Malaysia

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

Yes

Description

Inclusion Criteria:

  • House Officers currently or previously trained in Department of Emergency Medicine Hospital USM
  • Medical Officers who received Housemanship Training in Department of Emergency Medicine Hospital USM within 1 year prior to study

Exclusion Criteria:

  • Participants who have previously underwent training in ultrasound-guided regional nerve block.

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Ultrasound-Guided Femoral Nerve Block Training Intervention
Junior doctors in the Emergency Department at Hospital Universiti Sains Malaysia will undergo a low-fidelity simulation-based training on ultrasound-guided femoral nerve block using a bovine meat model. The intervention includes a brief lecture, demonstration, and hands-on practice session, followed by assessment of knowledge (MCQ) and skills (OSCE) pre- and post-intervention.
This intervention involves a low-fidelity simulation-based training on ultrasound-guided femoral nerve block (UGFNB) using a bovine meat model. Participants receive a brief lecture followed by a hands-on skills session. The training focuses on anatomical identification, ultrasound imaging, and nerve block technique using the simulated model. Knowledge and skill performance are assessed through multiple-choice questions and an OSCE before and after the intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in knowledge score before and after training
Time Frame: Immediately before and after the intervention (within same day)
Knowledge will be assessed using a validated 10-item multiple choice questionnaire. Total score ranges from 0 to 10.
Immediately before and after the intervention (within same day)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in procedural skill score (OSCE) before and after training
Time Frame: Immediately before and after the intervention
Skill will be assessed using a structured 7-domain OSCE checklist. Total score ranges from 0 to 20.
Immediately before and after the intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported confidence level in performing ultrasound-guided femoral nerve block post training
Time Frame: Immediately after intervention
Participants will self-report their confidence using a survey immediately following the simulation training. Data will describe participants' post-training confidence and prior exposure to regional anesthesia.
Immediately after intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Dr Mohamad Zikri Bin Ahmad, Department of Emergency Medicine, Universiti Sains Malaysia
  • Principal Investigator: Dr Ahmad Afiq Bin Abdullah Zan, MBBCh, Department of Emergency Medicine, Universiti Sains Malaysia

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)

August 1, 2025

Primary Completion (Actual)

May 12, 2026

Study Completion (Estimated)

May 12, 2026

Study Registration Dates

First Submitted

May 16, 2026

First Submitted That Met QC Criteria

May 16, 2026

First Posted (Actual)

May 22, 2026

Study Record Updates

Last Update Posted (Actual)

May 22, 2026

Last Update Submitted That Met QC Criteria

May 16, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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