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Simulated-based Program for Peripheral Nerve Blocks in Anesthesia Residents

Sponsor
Pontificia Universidad Catolica de Chile (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06081790
Collaborator
(none)
12
Enrollment
11
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

The goal of this Simulated Based Program for Peripheral Nerve Blocks is build learning curves in anesthesia residents.

The research questions are:

How behave the learning curves in a simulate based training program in peripheral nerve blocks in anesthesia residents? Does the learning achieved during the program transferred to the real patient's scenario?

Participants will be subjected to 10 simulated training sessions of a sciatic popliteal nerve block, subsequently their performance will be recorded and a global scale will be applied and movements will be measured. In a second stage, the same subjects will perform a block on a real patient to determine the transfer of this simulated learning.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    12 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Simulated-based Training Program for Peripheral Nerve Blocks Under Ultrasound, in Anesthesia Residents: Learning Curve and Transference
    Anticipated Study Start Date :
    Nov 1, 2023
    Anticipated Primary Completion Date :
    Apr 4, 2024
    Anticipated Study Completion Date :
    Sep 30, 2024

    Outcome Measures

    Primary Outcome Measures

    1. observational global rating scale scores (GRS) [Pre-intervention: first measurement before simulated-based training. During intervention: We will assess participants after each training session during 10 weeks. Post intervention: measurement once finished the protocol. Up to 12 weeks]

      At the end of the training, residents performance will be asses using a previous validated GRS (points 0-50)

    Secondary Outcome Measures

    1. Total path length (TPL) [Pre-intervention: first measurement before simulated-based training. During intervention: We will assess participants after each training session during 10 weeks. Post intervention: measurement once finished the protocol. Up to 12 weeks]

      At the end of the training, residents performance will be asses using a hands tracking motion device that measured TPL of both hand in meters

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Anesthesia first year residents
    Exclusion Criteria:

    • Previous regional anesthesia rotation

    • Previous training in ultrasound guided punction

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Pontificia Universidad Catolica de Chile

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Pablo Miranda, MD, assistant professor, Pontificia Universidad Catolica de Chile
    ClinicalTrials.gov Identifier:
    NCT06081790
    Other Study ID Numbers:
    • 230316005
    First Posted:
    Oct 13, 2023
    Last Update Posted:
    Oct 18, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Oct 18, 2023