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Deliberate Practice With Validated Metrics Improves Skills Acquisition

1 maj 2018 uppdaterad av: Osman Ahmed, University College Cork

Deliberate Practice With Validated Metrics Improves Skill Acquisition in Performance of Ultrasound Guided Peripheral Nerve Block in a Simulated Setting

Purpose:

The aim of this study was to compare the effects of deliberate vs. self-guided practices on acquiring needling skills by novice learners.

Methods:

Eighteen medical students were randomized to deliberate or self-guided practices groups. Following a learning phase, subjects attempted to perform a predefined task, which entitled advancing a needle towards a target on a phantom gel under ultrasound guidance. Subsequently, all subjects practiced performing the task using previously validated metrics. Subjects in the deliberate practice group were coached by an expert anesthesiologist and practiced each metric until it was satisfactorily performed based on the supervising anesthesiologist assessment. Immediately after completing the practice, all subjects attempted to perform same task, and on the following day, made two further attempts in succession. Two trained consultant anesthesiologists will use the metrics to independently score the video-recorded performances.

Studieöversikt

Detaljerad beskrivning

Safe performance of ultrasound-guided peripheral nerve blocks (PNB) requires competence across a range of technical and nontechnical skills. Correct placement of a needle close to a nerve or plexus is critical to safe and successful procedure performance. Failure to maintain needle visibility while in forward motion may cause iatrogenic injury to nerves and surrounding structures, and is a "quality compromising" behavior in the early part of novice learning curve. Skills related to needle guidance are difficult to learn, as they require integration of multiple cognitive and psychomotor elements.

The objective of this study was to compare the effects of expert supervised deliberate practice with validated metrics vs. self-guided practice on novice needling skill acquisition as evaluated by the number of steps completed and errors made.

Methods

Having obtained informed written consent from each, eighteen 3rd and 4th year medical students with no previous experience of ultrasound-guided procedures were recruited. Each student provided demographic information on his or her age, gender and handedness. All subjects will attend a didactic lecture (learning phase) delivered in standard fashion by one investigator. This included outlines of ultrasound physics, scanning and practical techniques.

Subsequently, subjects will be randomly allocated using computer generated random numbers to one of two groups; self-guided practice (SP) and deliberate practice (DP). Approximately 24 hours after completion of the learning phase each subject will attempt to perform the following set of tasks (baseline assessment).

Task description (i) Perform ultrasonography of the phantom provided to identify embedded objects.

(ii) Identify verbally the structure at the 8 O'clock position (in reference to the ultrasound training block model) and surrounding structures.

(iii) Once the ultrasound image is deemed optimal, advance a 50 mm, 20 gauge block needle provided under ultrasound guidance towards the object at the 8 O'clock position.

(iv) Once the needle tip is deemed close enough to the object, inject 0.5 ml of saline.

Following the first set of tasks (baseline assessment), all subjects were allowed to practice the task using the list of metrics and according to their random group allocation.

Methods of practice allowed SP Group: An investigator will provide subjects in this group a list of metrics (steps and errors) extracted from a previously validated tool. They will be allowed to practice the task using the metrics list. When the subject declares readiness to progress to the assessment, training will be complete.

DP Group: A trained consultant anesthesiologist (expert in ultrasound-guided PNB and who regularly undertakes training of novices in these procedures) will supervise deliberate practice to each subject in this group using the metrics list. Subjects in this group will practice each item of the metric list until it is satisfactorily performed as assessed by the supervising anesthesiologist at which time training is deemed complete.

Immediately after completion of either self-guided practice or deliberate practice (training phase), all subjects in both groups will attempt the same task above (assessment 1). All subjects will also attempt the same task twice in succession on the following day (assessment 2 and 3).

All performances (baseline and 1- 3) will be videotaped using a head-mounted camera placed on subject's head. The first person video and ultrasound images record concurrently (time synchronized).

Two consultant anesthesiologists (each expert in performing PNB and who regularly train novices) will independently score the videos using the composite metrics list for number of steps completed and number of errors made (primary outcome).

Data and Statistical Analysis Differences in performances between the two groups for both primary and secondary outcomes will be examined for significance with one-factor analyses of variance (ANOVA).

The inter rater reliability (IRR) will be calculated according to proportionate agreement between the two video assessors "number of agreements/number of [agreements+disagreements]". IRR is considered to be acceptable if it was ≥ 0.8. Scores from both video assessors will be averaged to calculate the number of steps completed and number of errors made (primary outcome).

Studietyp

Interventionell

Inskrivning (Faktisk)

18

Fas

  • Inte tillämpbar

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • 3rd and 4th year medical students

Exclusion Criteria:

  • previous performance of ultrasound guided procedures

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Övrig
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Övrig: deliberate practice
expert supervised practice with validated metrics
Övrig: self-guided practice
self guided practice with validated metrics

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
number of steps completed and errors made
Tidsram: up to 24 hours
averaged score of the two video assessors is calculated for number of steps completed and error made
up to 24 hours

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

20 september 2016

Primärt slutförande (Faktisk)

1 oktober 2017

Avslutad studie (Faktisk)

1 februari 2018

Studieregistreringsdatum

Först inskickad

12 maj 2017

Först inskickad som uppfyllde QC-kriterierna

15 maj 2017

Första postat (Faktisk)

16 maj 2017

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

2 maj 2018

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

1 maj 2018

Senast verifierad

1 maj 2018

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 27th April, 2016.

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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