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Simulated-based Program for Peripheral Nerve Blocks in Anesthesia Residents

Simulated-based Training Program for Peripheral Nerve Blocks Under Ultrasound, in Anesthesia Residents: Learning Curve and Transference

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06081790
Enrollment
12
Registered
2023-10-13
Start date
2023-11-01
Completion date
2024-09-30
Last updated
2023-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Simulated - Based Training

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.

Interventions

None listed

Sponsors

Pontificia Universidad Catolica de Chile
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

\- Anesthesia first year residents

Exclusion criteria

* Previous regional anesthesia rotation * Previous training in ultrasound guided punction

Design outcomes

Primary

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

Secondary

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

Contacts

Primary ContactPablo F Miranda Hiriart, MD
pablofmh@gmail.com997062125

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026