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Creating a Proficiency-Based Virtual Reality Simulation Training Programme for Laparoscopic Assisted Colectomy (LAC)

6. Oktober 2008 aktualisiert von: Royal College of Surgeons, Ireland

Creating and Implementing a Proficiency-Based Progression Virtual Reality Training Programme for Higher Surgical Trainees for Laparoscopic Assisted Sigmoid Colectomy.

Laparoscopic Colectomy is an advanced minimally invasive procedure that requires advanced laparoscopic skills.

Minimally invasive surgery offers many advantages to the patients but exposes the surgeon to new challenges, many of which are human factor in nature. This in turn prolongs the learning curve and has delayed the widespread adoption of minimally invasive surgical techniques in the management of patients with colorectal disease.

Virtual reality simulation offers an effective way of training whereby surgical trainees can train repeatedly and achieve proficiency in a shorter time and a safe environment.

Studienübersicht

Detaillierte Beschreibung

Introduction:

Minimally Invasive Surgery (MIS) has conferred considerable advantages on patient's post operative outcome and recovery when compared with open surgery.

Major clinical trials including; Clinical Outcomes of Surgical Therapy Study Group (COSTSG), Colon Cancer Laparoscopic or Open Resection (COLOR), and Conventional vs. Laparoscopic-Assisted Surgery in Colorectal Cancer (CLASICC) have uniformly and consistently shown a significant reduction in the post operative pain, the use of narcotics and oral analgesics, and length of hospital stay, as well as a faster resumption of diet, return of bowel function when using a MIS approach.

Despite all these advantages to the patients, MIS imposed a significant difficulty on the surgeons. These difficulties were primarily human factor in nature.

The use of Virtual Reality (VR) simulation has been proven to help in the acquisition of MIS skills. The use of proficiency-based, virtual reality simulation should help training of MIS providers in a safe environment where complex tasks can be repeated as many times as needed to achieve a pre-set proficiency level. A well designed proficiency-based simulation curriculum should help the widespread use of the MIS approach.

Aims

Primary:

We aim to prove that subjects randomised to train under a proficiency-based progression simulation curriculum (SC) will learn to perform laparoscopic assisted colectomy faster, complete more surgical steps and commit fewer operative errors compared to subjects randomised to the current surgical training curriculum (CC)

Secondary:

We aim to set the institutional and national proficiency level for Laparoscopic Assisted Colectomy (LAC) using the ProMIS-LAC simulator from Haptica, Ireland.

Methods Randomised, controlled, single blinded, multicentre study. Primary Variable 8 centres, 8 co-investigators (expert consultant laparoscopic colorectal surgeons > 300 MIS procedures) and 16 surgical trainees will be recruited for the study. Subjects (surgical trainees) will be randomised into;

  • Simulator Curriculum (SC) group.
  • Conventional Curriculum (CC) group.

Subjects randomised to the CC group will continue to have the conventional training programme offered at their respective hospitals. Subjects randomised to the SC group will complete a standardised laparoscopic skills training course followed by a training curriculum including the performance of simulated LAC procedures in nine predetermined steps on the simulator. Subjects must reach a predetermined proficiency level to complete the simulation training course before re-joining their training programme offered at their respective hospitals. .

Upon completion of the training courses, both groups' subject populations will perform a total of five LAC procedures on consecutive patients in the presence of a surgeon proctor.

Patients indicated for LAC procedure will be screened, consented, and enrolled as patients into this study. Each procedure will be recorded and forwarded to the chief investigator for analysis. The number of completed surgical steps and the incidence of intraoperative errors between the two SC and CC groups will be evaluated via blinded video review.

Secondary Variable

All participating co-investigators will participate in defining the proficiency level for LAC on the ProMIS-LAC simulator.

The average values of the recorded metrics which are obtained from the expert performance will be used to set the proficiency level.

Studientyp

Interventionell

Einschreibung (Voraussichtlich)

16

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Cork, Irland
        • Rekrutierung
        • Mercy University Hospital
        • Kontakt:
          • Michael O'Riordain, MD, FRCS
          • Telefonnummer: +353 21 4935336
        • Unterermittler:
          • Michael O'Riordain, MD, FRCSI
      • Dublin, Irland, 24
        • Rekrutierung
        • AMNCH
        • Kontakt:
          • Dairmuid O'Riordain, MD, FRCSI
          • Telefonnummer: +353 1 414 2213
        • Unterermittler:
          • Dairmuid O'Riordain, MD, FRCSI
      • Dublin, Irland, 4
        • Rekrutierung
        • St. Vincent's University Hospital
        • Kontakt:
          • Desmond Winter, MD, FRCSI
          • Telefonnummer: +353 1 2214000
        • Unterermittler:
          • Desmond Winter, MD, FRCSI
      • Dublin, Irland, 9
        • Rekrutierung
        • Beaumont Hospital
        • Kontakt:
          • Deborah McNamara, MD, FRCSI
          • Telefonnummer: +353 1 8093000
        • Unterermittler:
          • Deborah McNamara, MD, FRCSI
      • Dublin, Irland, Co. Dublin
        • Rekrutierung
        • AMNCH
        • Kontakt:
          • Paul Neary, MD, FRCSI
          • Telefonnummer: +35314142000
        • Hauptermittler:
          • Paul Neary, MD, FRCSI
      • Tullamore, Irland, Co Offaly
        • Rekrutierung
        • Tullamore general hospital
        • Kontakt:
          • Dermot Hehir, FRCSI
          • Telefonnummer: +35357 93 22206
        • Unterermittler:
          • Dermot Hehir, FRCSI
      • Antrim, Vereinigtes Königreich
        • Rekrutierung
        • Antrim Area Hospital
        • Kontakt:
          • Colman Byrnes, MD, FRCS
          • Telefonnummer: +44 028 9442 4000
        • Unterermittler:
          • Colman Byrnes, Md, FRCS
      • Glasgow, Vereinigtes Königreich
        • Rekrutierung
        • Gartnavel General Hospital
        • Kontakt:
          • Richard Molloy, MD, FRCS
          • Telefonnummer: +44 1412113483
        • Unterermittler:
          • Richard Molloy, MD, FRCS
      • Leicester, Vereinigtes Königreich
        • Rekrutierung
        • Leicester Royal Infirmary Hospital
        • Kontakt:
          • Andrew Miller, MD, FRCS
          • Telefonnummer: +44 116 2586853
        • Unterermittler:
          • Andrew Miller, MD, FRCS
      • Newcastle, Vereinigtes Königreich
        • Rekrutierung
        • Freeman Hospital
        • Kontakt:
          • Alan Horgan, MD, FRCS
          • Telefonnummer: +44 191 2137420
        • Unterermittler:
          • Alan Horgan, MD, FRCS

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion criteria for subjects

  • Classified as year 3-5 post graduation registrars, specialist registrars or residents in surgery.
  • Completed their Basic Surgical Training programme.
  • Completed at least 12 months period on a Higher Surgical Training programme.
  • In an accredited surgical post at time of participation
  • In a colorectal surgery rotation at time of participation
  • Signed their own consent form

Exclusion criteria for subjects

  • Performed, as primary surgeon, > 10 advanced laparoscopic procedures (laparoscopic cholecystectomy, inguinal hernia, appendectomy, Nissen fundoplication, or ventral incisional hernia repair are not considered advanced laparoscopic procedures )
  • Performed, as primary surgeon, laparoscopic assisted colectomy procedures
  • Performed, as primary surgeon, any hand-assisted laparoscopic colectomy procedures
  • Did not sign their own consent form

Inclusion criteria for patients

  • Indicated for a laparoscopic assisted sigmoid colectomy or high anterior resection
  • At least 18 years old upon date of signing the informed consent document (ICD)
  • Sign their own ICD

Exclusion criteria for patients

  • History or current diagnosis of synchronous colon cancer
  • Indicated for urgent surgery
  • Indicated for diverting stoma
  • American Society of Anaesthesiologists (ASA) Classification of Physical Status IV-V
  • Tumour classified as T4
  • An obstructed colon
  • Planned early conversion based on findings at operative visualisation.
  • Pregnancy
  • < 18 years of age
  • Mental disability
  • Did not sign their own ICD

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Single

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: SC
Subjects (surgical trainees) randomised to train under a proficiency-based progression virtual reality simulation curriculum
Subjects (surgical trainees) will be trained under a proficiency-based virtual reality simulation training programme before performing their first live case
Andere Namen:
  • Simulation Curriculum
  • SC
Aktiver Komparator: CC
Subjects (surgical trainees) randomised to the current surgical training curriculum
Subjects (surgical trainees) will continue to train under the current training methodology offered at their institution before they perform their first live case.
Andere Namen:
  • CC
  • Current Curriculum

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Subjects randomised to train under a proficiency-based simulation curriculum (SC) will perform laparoscopic assisted colectomy faster, complete more surgical steps and commit fewer operative errors compared to subjects randomised to the control group
Zeitfenster: 6-12 months
6-12 months

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
We aim to set the institutional and national proficiency level for Laparoscopic Assisted Colectomy (LAC) using the ProMIS-LAC simulator from Haptica, Ireland.
Zeitfenster: 30 days
30 days

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Paul Neary, MD, FRCSI, Royal College of Surgeons in Ireland

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. September 2008

Primärer Abschluss (Voraussichtlich)

1. Juni 2009

Studienabschluss (Voraussichtlich)

1. September 2009

Studienanmeldedaten

Zuerst eingereicht

11. September 2008

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

12. September 2008

Zuerst gepostet (Schätzen)

15. September 2008

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

7. Oktober 2008

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

6. Oktober 2008

Zuletzt verifiziert

1. Oktober 2008

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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