Metric-based Feedback Training for the Acquisition of Sonographic Skills
NCT ID: NCT02976623
Last Updated: 2017-05-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
13 participants
INTERVENTIONAL
2016-06-30
2017-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The objective of this study was to determine the effect of a structured, objective and terminal feedback on novices' performance skills of ultrasonography part of ultrasound-guided axillary brachial plexus block.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Evaluation of the Ultrasound-guided Clinical Procedure Simulation Curriculum
NCT04792203
Application of Intermittent Training in Radial Artery Puncture and Catheterization Skills Under Ultrasound-Guided Line Guidance
NCT07248683
Learning From Errors During Simulation-based Ultrasound Training
NCT02369640
Analysis of the Effect of Pre-course Videos on Improving Clinical Skills in Emergency Ultrasound Training
NCT06947733
Effect of the Use of a Visual Feedback Device in RCP Trainings
NCT04338490
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The objective of this study was to determine the effect of a structured, objective and terminal feedback on novices' performance skills of ultrasonography part of ultrasound-guided axillary brachial plexus block.
Methods:
With institutional ethical approval and having obtained written informed consent from each, 12 anesthesia trainees will be invited to participate in this prospective, randomized and blinded study.
Inclusion criteria:
i. trainees in the Irish national anesthesia training program allocated to Cork teaching hospital (CUH) ii. have performed no more than 5 ultrasound-guided peripheral nerve blocks at the time of participation.
Each participant will answer tests to ascertain visuospatial and perceptual abilities (card rotation, cube comparisons and map planning tests).
Each participant will provide baseline information prior to participation i) age ii) gender iii) handedness iv) Years since graduating from medical school v) number or estimated number of previously performed ultrasound-guided interventional procedures including securing vascular access vi) courses/workshops in ultrasound-guided procedural interventions.
All participants will receive a standard learning in the form of i) a one hour didactic lecture delivered by a single investigator which outlines basic sonographic anatomy, ultrasound physics and anatomy relevant to performing ultrasound-guided axillary brachial plexus block.
Within 24 hours of completing the learning phase, participants will be asked to perform ultrasonography of left axilla of a volunteer. This will be followed by either feedback A or feedback B (based on random allocation). Feedback will terminal, summative and commence five minutes after each participant completed the tasks.
Task description:
1. Participant perform ultrasonography of left axilla and adjacent upper limb as if preparing to perform ultrasound-guided axillary brachial plexus block
2. Participant identify the four terminal branches of the brachial plexus; identify each on the screen by using the pointer provided (or freeze image and use arrow on the screen) and name each verbally.
3. Participant identify the adjacent structures/vessels relevant to the block by indicating them individually using the pointer provided (or freeze image and use arrow on the screen) and name each verbally.
4. Once participant have obtained an optimal ultrasound image, participant is requested to indicate the intended needle insertion point on the skin using the pointer provided.
Participants will be provided with an opportunity to practice performing the tasks for up to 30 minutes. Within one hour of completing the feedback session, participants will be asked to attempt the same tasks again. Performance before and after feedback delivered will be video-recorded according to a predefined protocol by a trained investigator. Imaging will be obtained by an investigator using a handheld camera. Concurrent ultrasound video images will be recorded using the Digital Video Recorder (DVR) feature of the Ultrasonics Tablet (Sonix Design Centre, B.K Ultrasound, Richmond, Canada). All video recordings will be edited using a video editing software (Apple Movie, version 10.0.5, Apple Computer Inc. USA) to present the procedure together with the ultrasound output on one screen
Types of Feedback:
i. Feedback A: Standard feedback; a consultant anesthetists will be asked to give feedback as would normally give during performance of such a task in a clinical situation.
ii. Feedback B: Structured feedback; a trained investigator will give feedback according to a set of metrics and errors previously developed and validated. Trainees will undergo deliberate practice on the volunteer until they demonstrate adequate and objective performance as assessed by the set of metrics and errors provided.
Video assessment and scoring:
Two trained, independent and blinded assessors will score the video recordings for a set of metrics and errors previously developed and validated. The number of steps completed and errors committed will be compared for i) Group defined by preceding type of feedback, ii) Pre versus post for each feedback session
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
feedback group
this group will receive the intervention "metric-based feedback training" on their performance. this will be based on validated metrics and errors, a trained investigator will deliver this feedback. It will be accompanied by deliberate practice
metric-based feedback training
Structured feedback; a trained investigator will give feedback according to a set of metrics and errors previously developed and validated. Trainees will undergo deliberate practice on the volunteer until they demonstrate adequate and objective performance as assessed by the set of metrics and errors provided.
control group
this control group will receive a standard type feedback on their performance "no intervention". It will be delivered by a consultant anaesthetist who will be instructed to deliver feedback as they ordinarily do during their clinical practice
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
metric-based feedback training
Structured feedback; a trained investigator will give feedback according to a set of metrics and errors previously developed and validated. Trainees will undergo deliberate practice on the volunteer until they demonstrate adequate and objective performance as assessed by the set of metrics and errors provided.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* having performed no more than 5 ultrasound-guided peripheral nerve blocks
Exclusion Criteria
* have performed more than 5 ultrasound-guided peripheral nerve blocks
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University College Cork
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Brian Declan O'Donnell
Consultant Anaesthetist, Senior Lecturer
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Cork University Hospital
Cork, , Ireland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ECM 4 (f) 19/01/16
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.