Feedback: The FEEDBACK Trial, a Randomized Controlled Trial

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Unknown status
CT.gov ID
NCT01497782
Collaborator
Copenhagen Trial Unit, Center for Clinical Intervention Research (Other)
99
1
2
9
11

Study Details

Study Description

Brief Summary

With a worldwide proliferation of simulation centers, it is essential to explore the optimal setting for laparoscopic training and investigate different learning approaches, e.g. a self-directed approach. Therefore, the researchers investigated the following in a randomized controlled trial: the impact of instructor feedback vs. an independent, self-directed approach when training a complex operational task on a laparoscopic virtual reality simulator.

The study hypothesis is that instructor feedback has a pivotal effect on surgical skills when training on a virtual reality simulator.

Condition or Disease Intervention/Treatment Phase
  • Other: Instructor feedback
N/A

Detailed Description

For virtual reality (VR) simulation the benefits are clear; the drawbacks are less clear. Throughout the last decade several studies have found a positive effect on the learning curve as well as improvement of basic psychomotor skills in the operating room after VR training. VR simulators offer standardized and reproducible laparoscopic tasks, ranging from simple basic skills training to full procedures such as a cholecystectomy or salpingectomy. Despite the now well-established advantages of VR simulators, the majority of surgical and gynecological departments encounter hurdles when implementing this form of training in the surgical education. This is mainly due to lack of knowledge concerning the time and human resources/cost needed to train novice surgeons to an adequate level.

This randomized trial investigates whether instructor feedback is pivotal for the trainee when training operational tasks (a laparoscopic salpingectomy) on a VR simulator. The VR simulator used in this trial is the LapSim from Surgical Science, Sweden. Instructor feedback consists of standardized feedback for ten minutes and with a maximum of three optional feedback sessions; the trainees (in the intervention group) decides them selves when they want a feedback session. The trainees in both the control group and the intervention group have to reach a predefined proficiency level on the VR simulator within 8 weeks with 3-hour training sessions each time. Furthermore, the trial focuses on different learning approaches, e.g. a self-directed approach and an independent approach.

The randomization process will take place at a central unit; Copenhagen Trial Unit, Denmark. Stratification variables are: 1)Gender 2)Computer game experience (less that 20 hours annually)

Study Design

Study Type:
Interventional
Actual Enrollment :
99 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
Impact of Instructor Feedback on Performance in a Virtual Reality Simulator: A Randomized, Controlled Trial
Study Start Date :
Apr 1, 2011
Actual Primary Completion Date :
Oct 1, 2011
Anticipated Study Completion Date :
Jan 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Instructor feedback

Intervention group who receives up to three sessions of instructor feedback during completion of a predefined proficiency level on a laparoscopic virtual reality simulator.

Other: Instructor feedback
Intervention group who receives up to three sessions of instructor feedback during completion of a predefined proficiency level on a laparoscopic virtual reality simulator.

No Intervention: No instructor feedback

Control group who did not receive instructor feedback during completion of a predefined proficiency level on a laparoscopic virtual reality simulator.

Outcome Measures

Primary Outcome Measures

  1. Repetitions [8 weeks]

    Number of repetitions to complete a predefined proficiency level on a laparoscopic virtual reality simulator

Secondary Outcome Measures

  1. Time [8 weeks]

    Time to complete a predefined proficiency level on a laparoscopic virtual reality simulator.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Medical student at Copenhagen University with passed bachelor degree

  • Signed informed consent

Exclusion Criteria:
  • Prior experience with surgical virtual reality simulators

  • 3 independent laparoscopic procedures

  • Not fluent in the Danish language

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rigshospitalet, University Hospital of Copenhagen Copenhagen Denmark 2100

Sponsors and Collaborators

  • Rigshospitalet, Denmark
  • Copenhagen Trial Unit, Center for Clinical Intervention Research

Investigators

  • Principal Investigator: Jeanett Oestergaard, MD, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jeanett Oestergaard, MD, PhD fellow, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT01497782
Other Study ID Numbers:
  • H-3-2010-082 FEEDBACK
First Posted:
Dec 22, 2011
Last Update Posted:
Dec 22, 2011
Last Verified:
Dec 1, 2011
Keywords provided by Jeanett Oestergaard, MD, PhD fellow, Rigshospitalet, Denmark

Study Results

No Results Posted as of Dec 22, 2011