Evaluation of a New Training Model for Ultrasound Guided Regional Anesthesia - A Feasibility Study

NCT ID: NCT02370472

Last Updated: 2018-03-02

Study Results

Results pending

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.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2015-02-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The use of Ultrasound Guided Regional Anaesthesia (USRA) has increased over the last decade. Theoretically, ultrasound imaging may increase efficacy and safety by allowing visualization of the needle pathway and local anaesthetic spread around the nerve. In addition to knowledge of anatomy and general principles of ultrasonography, USRA requires learning new skills such as image interpretation, needle-beam alignment, and needle trajectory tracking. The hand-eye coordination required during needle advancement requires practice to master because the needle must be properly aligned with the ultrasound probe in order to maintain the needle path in the beam at all times. Adding to the difficulty, hand and needle movements can occur in three axes, but an ultrasound image is seen in only two dimensions. Since the ability to acquire the necessary skills to perform USRA is subjective and not yet validated, it is difficult to recommend a single, effective training pathway.

Currently, the only method of supervised training before performing an USRA procedure on an actual patient involves practicing needle insertion in a phantom or cadaver. Studies assessing the impact of learning using these methods are lacking. It is possible that some practitioners may choose alternative one-off learning methods. Such methods are not standardized and are thus difficult to evaluate.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This was a single site, prospective, pre-test-post-test, randomized study conducted after Institutional Review Board (IRB) approval. Thirty subjects, including medical students, practicing anaesthesiologists and anaesthesia residents in training at the Penn State Hershey Medical Center, were recruited by formal email invitation to participate. Written consent was obtained from each participant before their inclusion in the study and each participant completed a pre-study form. Once enrolled in the study, participants were given 10 minutes to familiarize themselves with both the ultrasound equipment (SonoSite, MTurbo, Bothell, WA, USA) and the phantom model (MiniSimâ„¢ Upper Extremity Series, Life tech Inc., Stafford, Texas, USA). They also viewed a pre-recorded video demonstrating the task they were to perform. As a pre-test, participants performed the required Needle Insertion Accuracy (NIA) task 3 consecutive times and were assessed using a scoring form adapted from the Mayo Clinic. After completing the pre-test, participants were randomly divided into two groups, experimental and control, by a computer-generated randomization list (SAS Institute, Cary, NC). Participants were blinded to their group assignment.

Previously, we have reported details of the new learning tool. Briefly, all spatial movements occur in three dimensions which can be labeled the x-axis, the y-axis and the z-axis. A video camera records movement in two axes. By placing a second video camera at 90 degrees to the first camera, the third axis can be recorded as well as one axis in common with the first camera. Video recordings are stored electronically on a hard-drive and can be reviewed individually or in combination, at normal speed, or slowed if necessary. Still images can also be obtained.

The experimental group was allowed to practice the same pre-test task using the same ultrasound machine and phantom model. On a single computer screen, they were able to visualize their hand and needle movements along with the position of the ultrasound probe. The control group was allowed to practice the same pre-test task using the same ultrasound machine and phantom model but without the added visual aid. Both groups were allowed to practice their pre-test tasks for a maximum of 30 minutes, and recorded their self-assessment as proficient or not proficient at that time. Both groups then performed the post-test, which was the same task used for the pre-test, and each trainee was evaluated using the same scoring tool. To avoid subjective variations and inter-rater variability, all evaluations were recorded by a single blinded investigator.

Statistical analysis Pre- and post-test mean scores (ranging from 5 to15) were analyzed using statistical methods to determine whether this new learning tool improved NIA skills required with USRA. Pre-test and post-test scores (ranging from 5 to 15) were obtained in triplicate and averaged to produce a representative assessment for each participant. The primary endpoint was change in NIA score from baseline, i.e., the score difference obtained by subtracting the mean pre-test score from the mean post-test score. A sample size of 15 subjects per group (experimental and control) provides 80% power to detect an effect size of 1, based on a two-sided t-test with a 5% error probability (calculated using G\*Power version 3.1). Analysis of the primary endpoint utilized a two-sided, two-sample t-test at the 5% level of significance. Secondary analyses evaluated the intervention effect on novice trainees, and trainees with prior USRA experience. Score differences for individual NIA skills (movement, alignment, approach, target, location) were also analyzed.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Regional Anesthesia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

control group

complete pre-study form 10 minute familiarization time with equipment view video demonstration of task perform task 3 times assessed using scoring form - pretest assigned to group practice task again for 30 minutes proficiency noted final evaluation

Group Type NO_INTERVENTION

No interventions assigned to this group

Experimental

complete pre-study form 10 minute familiarization time with equipment view video demonstration of task perform task 3 times assessed using scoring form - pretest assigned to group practice task again for 30 minutes - subjects will use tool developed using cameras and a computer to visualize hand and needle movements as well as the position of the transducers along with the image from the ultrasound on a computer screen proficiency belief noted final evaluation

Group Type EXPERIMENTAL

tool developed using cameras and a computer

Intervention Type OTHER

cameras allowing subject to be able to visualize hand and needle movements as well s the position of the transducers along with the image from the ultrasound on a computer screen

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

tool developed using cameras and a computer

cameras allowing subject to be able to visualize hand and needle movements as well s the position of the transducers along with the image from the ultrasound on a computer screen

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Health Care professional

Exclusion Criteria

* None
Minimum Eligible Age

25 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Milton S. Hershey Medical Center

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Sanjib Adhikary

Associate Professor , Director Acute Pain, Regional Anesthesia/Orthopedics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Sanjib Adhikary, MB BS MD

Role: PRINCIPAL_INVESTIGATOR

Milton S. Hershey Medical Center

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Penn State Hershey Medical Center

Hershey, Pennsylvania, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

Sites BD, Chan VW, Neal JM, Weller R, Grau T, Koscielniak-Nielsen ZJ, Ivani G. The American Society of Regional Anesthesia and Pain Medicine and the European Society of Regional Anaesthesia and Pain Therapy joint committee recommendations for education and training in ultrasound-guided regional anesthesia. Reg Anesth Pain Med. 2010 Mar-Apr;35(2 Suppl):S74-80. doi: 10.1097/AAP.0b013e3181d34ff5.

Reference Type RESULT
PMID: 20216029 (View on PubMed)

Ramlogan R, Manickam B, Chan VW, Liang L, Adhikary SD, Liguori GA, Hargett MJ, Brull R. Challenges and training tools associated with the practice of ultrasound-guided regional anesthesia: a survey of the American society of regional anesthesia and pain medicine. Reg Anesth Pain Med. 2010 Mar-Apr;35(2):224-6. doi: 10.1097/AAP.0b013e3181c69c94. No abstract available.

Reference Type RESULT
PMID: 20216042 (View on PubMed)

Adhikary SD, Hadzic A, McQuillan PM. Simulator for teaching hand-eye coordination during ultrasound-guided regional anaesthesia. Br J Anaesth. 2013 Nov;111(5):844-5. doi: 10.1093/bja/aet364. No abstract available.

Reference Type RESULT
PMID: 24108733 (View on PubMed)

Smith HM, Kopp SL, Jacob AK, Torsher LC, Hebl JR. Designing and implementing a comprehensive learner-centered regional anesthesia curriculum. Reg Anesth Pain Med. 2009 Mar-Apr;34(2):88-94. doi: 10.1097/AAP.0b013e31819e734f. No abstract available.

Reference Type RESULT
PMID: 19282705 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

38067

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Noninvasive Modulation of Chronic Neuropathic Pain
NCT06249724 WITHDRAWN PHASE1/PHASE2
Low-intensity Focused Ultrasound and Autonomic Response
NCT05834829 ENROLLING_BY_INVITATION NA