MD-VR-THA: VR Simulation and Basic Skills in THA

Sponsor
Aristotle University Of Thessaloniki (Other)
Overall Status
Recruiting
CT.gov ID
NCT05807828
Collaborator
(none)
60
1
2
5.2
11.6

Study Details

Study Description

Brief Summary

This prospective randomised clinical trial aims to test if virtual reality (VR) simulation helps acquire basic surgical skills in total hip arthroplasty (THA) by medical students.

The main question[s] it aims to answer are:
  1. Can VR simulation develop the medical students' basic surgical skills and medical knowledge in THA?

  2. Will VR simulation become a part of orthopaedic surgical education?

Participants will be randomised into two groups (VR and control).

  1. They will be asked to watch a very detailed video explaining basic rules and skills in implanting the acetabular cup and femoral stem in THA

  2. The VR group will perform at least three VR THA sessions concerning cup (inclination) and stem (version) implantation

  3. Then all participants will be asked to implant a cup and a stem in a predefined inclination and version, respectively, in sawbones

  4. The mean difference between the predefined and the actual implanted cup inclination and version of the stem will be compared between groups

Condition or Disease Intervention/Treatment Phase
  • Procedure: VR simulation on basic THA skills
N/A

Detailed Description

This study is a prospective randomized controlled trial and received approval from the A.U.Th. Institutional Review Board.

Eligible study participants include undergraduate medical students at our university.

Exclusion criteria include a. postgraduate medical students b. prior experience in THA or general surgery.

One week before the planned VR-THA surgery session, all eligible A.U.Th. Medical students will be invited to an information session regarding the study and will be voluntarily enrolled, providing inform consent.

Medical students were explicitly chosen for participation because they are surgically naïve and would most likely benefit from basic skills training in THA.

Immediately after enrollment, medical students will be asked to complete a multiple-choice pretest to quantify their baseline medical and procedural knowledge of hip arthritis and THA. All participants will be unaware and unable to prepare for the pretest assessment, which allows the test scores to be considered an accurate measure of baseline knowledge.

The medical students will be asked to watch a detailed video explaining basic rules and skills for implanting the acetabular cup and femoral stem in THA. The video will be focused on practices and methods to achieve specific cup inclination and stem version during implantation.

All participants will be randomized to the VR simulation or control group for cup inclination assessment by a computerized random number generator. Participants will be privately notified of their randomization by e-mail and asked not to disclose their designated cohort with any other study participant or research personnel. Only a research team member will be aware of the cohort assignments during this study. The participants enrolled on the VR group for cup inclination will be the control group for the stem version group and vice versa.

Before the VR-THA, participants will be asked to complete a survey evaluating their previous video games and VR technology experience.

All control group participants will then be asked to implant a cup or a stem in a predefined inclination and version in sawbones. The cup inclination and stem version will be evaluated using specific goniometers and assessment of photographs taken during implantation. The evaluation will be performed by study personnel unaware of the participants' group assignment.

All VR group participants will then be asked to complete three consecutive VR sessions using the VR system (ORama VR, Geneva, Switzerland), performing cup or stem implantation based on their group. All VR group participants will then be asked to implant a cup or a stem in a predefined inclination and version in sawbones. The cup inclination and stem version will be evaluated using the same specific goniometers and assessment of photographs that will be taken during implantation. The evaluation will be performed by the same study personnel unaware of the participants' group assignment. This personnel will also record the time needed for implantation.

During implantation in sawbones, a study assistant will be present who will be instructed to intervene only if the study participants request assistance or cannot progress through the task.

Upon completion of the VR-THAs, participants will complete a survey focused on their interest in using VR simulations for surgical skills training and assessing for potential negative consequences. Power analysis was performed, indicating that more than 30 participants will be necessarily enrolled in each group.

The primary outcome will be the mean difference between the asked predefined and the actual implanted cup inclination or cup version between the control and VR groups.

The secondary outcomes will be

  1. the percentage difference of the target approach between the asked and the actual implanted cup inclination or cup version for each participant performing implantation (one task will be performed as the VR and the other as the control group).

  2. Differences in completing the task between groups will also be recorded ( time needed to complete the task and asking for assistance).

Two weeks later, all participants will perform the implantation on sawbones once again.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
All participants will be randomized to the VR simulation or control group for cup inclination and stem version assessment by a computerized random number generator. The VR group will perform implantation on sawbones after VR education and the control group without VR education.All participants will be randomized to the VR simulation or control group for cup inclination and stem version assessment by a computerized random number generator. The VR group will perform implantation on sawbones after VR education and the control group without VR education.
Masking:
Single (Outcomes Assessor)
Masking Description:
The personnel that will assess the cup inclination and stem version will not know the group assignment of the participants
Primary Purpose:
Other
Official Title:
The Role of Virtual Reality Simulation in Acquiring Basic Surgical Skills in Total Hip Arthroplasty by Medical Students- a Prospective Randomized Clinical Trial
Actual Study Start Date :
Mar 26, 2023
Anticipated Primary Completion Date :
May 31, 2023
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Control Group

This group will include medical students who will only watch instructional videos on basic THA skills on the cup and stem implantation before actual implantation on sawbones

Procedure: VR simulation on basic THA skills
The medical students' VR group will perform three VR simulation sessions on basic THA skills on the cup and stem implantation before actual implantation.

Other: VR Group

This group will include medical students who will watch instructional videos and perform three consecutive VR sessions on basic THA skills on the cup and stem implantation before actual implantation on sawbones

Procedure: VR simulation on basic THA skills
The medical students' VR group will perform three VR simulation sessions on basic THA skills on the cup and stem implantation before actual implantation.

Outcome Measures

Primary Outcome Measures

  1. Medical students surgical skills differences between VR and control group. [2 Months]

    The primary outcome will be the mean difference between the asked predefined and the actual implanted cup inclination or cup version between the control and VR groups.

Secondary Outcome Measures

  1. Surgical skills differences between cup and stem implantation for each medical student (the one implantation will be performed following VR training and the other not) [2 months]

    The secondary outcome will be the percentage difference of the target approach between the asked and the actual implanted cup inclination or cup version for each participant performing implantation. Differences in completing the task between groups will also be recorded ( time needed to complete the task and asking for assistance).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 24 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  1. undergraduate medical students at Aristotle University of Thessaloniki
Exclusion criteria:
  1. postgraduate medical students

  2. prior experience in THA or general surgery.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aristotle University Medical School Thessaloniki Greece

Sponsors and Collaborators

  • Aristotle University Of Thessaloniki

Investigators

  • Principal Investigator: Eleftherios Tsiridis, Professor, Aristotle University Medical School

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Eustathios Kenanidis, Assistant Professor of Orthopaedic Surgery & Traumatology, Aristotle University Of Thessaloniki
ClinicalTrials.gov Identifier:
NCT05807828
Other Study ID Numbers:
  • 79/2023
First Posted:
Apr 11, 2023
Last Update Posted:
Apr 11, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eustathios Kenanidis, Assistant Professor of Orthopaedic Surgery & Traumatology, Aristotle University Of Thessaloniki
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 11, 2023