Mastery Learning Inguinal Hernia Repair

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01085500
Collaborator
National Center for Research Resources (NCRR) (NIH)
50
1
2
14.9
3.4

Study Details

Study Description

Brief Summary

Abstract: Minimally invasive techniques are now ubiquitous in the management of surgical disease. Competence in laparoscopy requires specialized training and practice. With the decrease of resident work hours, training programs need to explore and adopt efficient strategies to teach and evaluate laparoscopic skills. For economic, ethical, and legal considerations, the operating room may no longer be the ideal environment for teaching these basic technical skills. There appears to be a role for simulation in response to this need. The transfer of laparoscopic skills learned in a simulated environment to the operating room has showed mixed results. Overall, it seems that surgical skills training outside the operating room is beneficial, but the best method(s) of designing, implementing and evaluating such skills curriculums have yet to be identified.

The laparoscopic totally extraperitoneal (TEP) inguinal hernia repair is an example of a procedure that is associated with a steep learning curve and requires mastery of basic laparoscopic skills. In addition, an increased recurrence and complication rates in the early learning curve of this procedure, underscores the importance of adequate training. The current practice of teaching the TEP repair in the operating room under an apprenticeship-based model is associated with increased operative time and costs. We propose that the training of surgical trainees outside the operating room with a structured, mastery oriented simulation-based curriculum will help reduce the learning curve of the TEP repair, improve operative performance, and decrease operative time and costs.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mastery Learning TEP Curriculum
  • Procedure: Current Practice
N/A

Detailed Description

Specific Aims:

Inguinal hernias are a common ailment of the general population. Their surgical management through a laparoscopic totally extraperitoneal (TEP) approach has been shown to lead to less discomfort and faster recovery than do classic open repairs with equal effectiveness. Nonetheless, the TEP repair has not been adopted widely because of concerns regarding a substantial learning curve. In addition, the current practice of teaching the TEP procedure in the operating room under an apprenticeship-based model is associated with increased operative time and cost. The training of surgeons in laparoscopic skills outside the operating room with simulation-based strategies has emerged as an attractive alternative. Many studies have demonstrated that trainees who practice laparoscopic skills in a simulated environment show improvement of those skills when tested in that same environment. Few studies however, have been able to demonstrate a direct correlation between such simulation training and improved performance in the operating room. It appears from these studies that surgical skills training outside the operating room is beneficial, but the best methods have yet to be identified.

Our long-term research goal is to explore and adopt efficient simulation-based strategies to teach and evaluate surgical skills to surgical trainees. Our objective for this study is to design and evaluate a simulation-based curriculum based upon the concepts of mastery learning theory (achievement of pre-specified expert-derived benchmarks without time constraints) and to develop an objective mean of assessing operative performance that will both aid in shortening the learning curve of the TEP inguinal hernia repair for surgical trainees. Our central hypothesis is that the training of surgery residents outside the operative room with simulation-based strategies, such as the TEP mastery learning curriculum will improve operative performance and reduce operative time during the TEP repair. The rationale for this study is that the identification of effective strategies to shorten the learning curve of the TEP repair that translate into decreased operative time will not only increase the adoption of the TEP repair with its inherent benefits to more candidate patients, but will also lead to substantial cost-savings and perhaps improved patient outcomes. We are especially well prepared to complete this study as we are a part of an academic referral center that treats a myriad of inguinal hernias patients and educates hundreds of surgical residents on a continuous basis.

Specific Aim 1: To compare the TEP mastery learning curriculum with the apprenticeship-based model of learning the TEP repair in the operative room on operative time and operative performance of TEP inguinal hernia repairs performed by surgical trainees.

Hypothesis 1a: Surgical trainees who undergo the TEP mastery learning curriculum will achieve lesser mean operative times while performing a TEP inguinal hernia repair when compared to those who followed the apprenticeship-based model.

Hypothesis 1b: Surgical trainees who undergo the TEP mastery learning curriculum will achieve greater mean operative performance scores while performing a TEP inguinal hernia repair when compared to those who followed the apprenticeship-based model.

Secondary Aim:

Compare the rate of TEP inguinal hernia repair post-operative complications, specifically urinary retention for patients operated on by surgical residents who underwent the mastery learning curriculum versus those who underwent the apprenticeship-based model.

This research is innovative because it will challenge the current paradigm of teaching basic laparoscopic skills in the operative room and will strive to link surgical education methods to objective patient level outcomes such as operative time and cost. At the completion of this project, it is our expectation that we will be better prepared to continue our efforts of translating new educational modalities/technologies to improve the delivery of healthcare. Our anticipated findings will have a relevant impact in how we educate the surgeons of tomorrow.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Official Title:
Mastery Learning Totally Extraperitoneal Inguinal Hernia Repair: Linking Surgical Simulation to Patient Level Outcomes
Study Start Date :
Feb 1, 2010
Actual Primary Completion Date :
Jan 1, 2011
Actual Study Completion Date :
May 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Simulation Curriculum

General surgery residents will undergo a simulation-based educational curriculum (Mastery Learning TEP Curriculum) on TEP hernia repair

Behavioral: Mastery Learning TEP Curriculum
A simulation-based educational curriculum
Other Names:
  • TEP Curriculum
  • Other: Current Practice

    General surgery residents will undergo current practice of learning how to perform the TEP repair in the operating room under direct supervision of the staff surgeon without any simulation pre-training.

    Procedure: Current Practice
    The current practice of learning how to perform the TEP repair in the operating room is under direct supervision of the staff surgeon without any simulation pre-training.

    Outcome Measures

    Primary Outcome Measures

    1. Participation-Corrected Operative Time [at first TEP procedure post-randomization; Due to surgical scheduling variability this can be anytime from 1 to 2 days following randomization to a week or two]

      Operative time was recorded with a standard stopwatch, began at the start of the operative case and ended when procedure was terminated. We realized that the operative time for poorly performing trainees could be faster than the time for more skilled trainees because the supervising surgeon would perform a greater proportion of the procedure. We calculated participation-corrected time as raw total time + the time of staff involvement: time_corrected = time_raw + (1-participation) x time_raw.

    Secondary Outcome Measures

    1. Operative Performance [at first TEP procedure post-randomization; due to surgical scheduling variability this can be anytime from 1 to 2 days following randomization to a week or two]

      The trained observer and the staff supervising surgeon graded operative performance independently using a global rating scale, Global Operative Assessment of Laparoscopic Skills (GOALS) immediately after each case, (1 rating per case if bilateral repair). The GOALS tool has been shown to be a valid and reliable tool to measure generic laparoscopic skills in the simulated environment and in the operating room, with good agreement between live and video-review ratings. The scores range from 6 to 30, a higher score indicates greater operative performance.

    2. Number of Hernia Repair Subjects With Post-Operative Urinary Retention [at first TEP procedure post-randomization, subjects were followed for the duration of hospital stay, an average of 1 night]

      Urinary retention is the inability to empty the bladder. This is an educational study for surgeons. The participants in the study are surgeons, and the participant flow, baseline characteristics and first two outcome measures are for the surgeons. During the part of the study reported for the third outcome measure, the first surgical procedure (TEP) after randomization, each surgeon had one subject. Therefore, this outcome measure is for the hernia patients or subjects.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • General surgery residents (male or female), regardless of age or previous laparoscopic experience, who are able to perform at least 2 TEP inguinal hernia repairs during the study period (January - December 2010)

    • Postgraduate Year (PGY) 1 to PGY 5 general surgery residents.

    • Have the procedure supervised by one of the following expert laparoscopic surgeons: Dr. David Farley, Dr. Bingener-Casey, Dr. Swain, Dr. Kendrick

    Exclusion Criteria:
    • PGY 1 designated preliminary residents (Urology, Orthopedics, Neurosurgery and Anesthesia) or PGY 1 non-designated preliminary residents who are applying to fields other than general surgery.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic Rochester Minnesota United States 55902

    Sponsors and Collaborators

    • Mayo Clinic
    • National Center for Research Resources (NCRR)

    Investigators

    • Principal Investigator: David R Farley, MD, Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    David R. Farley, PI, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT01085500
    Other Study ID Numbers:
    • 09-008118
    • 1UL1RR024150
    First Posted:
    Mar 12, 2010
    Last Update Posted:
    Oct 28, 2016
    Last Verified:
    Sep 1, 2016
    Keywords provided by David R. Farley, PI, Mayo Clinic
    Additional relevant MeSH terms:

    Study Results

    Participant Flow

    Recruitment Details General surgery residents were recruited from the Mayo Clinic, Rochester, Minnesota from January to September 2010.
    Pre-assignment Detail
    Arm/Group Title Simulation Curriculum Current Practice
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice.
    Period Title: Overall Study
    STARTED 26 24
    COMPLETED 26 24
    NOT COMPLETED 0 0

    Baseline Characteristics

    Arm/Group Title Simulation Curriculum Current Practice Total
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice. Total of all reporting groups
    Overall Participants 26 24 50
    Age (Count of Participants)
    <=18 years
    0
    0%
    0
    0%
    0
    0%
    Between 18 and 65 years
    26
    100%
    24
    100%
    50
    100%
    >=65 years
    0
    0%
    0
    0%
    0
    0%
    Age (years) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [years]
    30
    (2)
    30
    (3)
    30
    (2)
    Sex: Female, Male (Count of Participants)
    Female
    9
    34.6%
    6
    25%
    15
    30%
    Male
    17
    65.4%
    18
    75%
    35
    70%
    Region of Enrollment (participants) [Number]
    United States
    26
    100%
    24
    100%
    50
    100%

    Outcome Measures

    1. Primary Outcome
    Title Participation-Corrected Operative Time
    Description Operative time was recorded with a standard stopwatch, began at the start of the operative case and ended when procedure was terminated. We realized that the operative time for poorly performing trainees could be faster than the time for more skilled trainees because the supervising surgeon would perform a greater proportion of the procedure. We calculated participation-corrected time as raw total time + the time of staff involvement: time_corrected = time_raw + (1-participation) x time_raw.
    Time Frame at first TEP procedure post-randomization; Due to surgical scheduling variability this can be anytime from 1 to 2 days following randomization to a week or two

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title Simulation Curriculum Current Practice
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice.
    Measure Participants 26 24
    Mean (Standard Deviation) [minutes]
    34.4
    (8.4)
    47.5
    (13.9)
    2. Secondary Outcome
    Title Operative Performance
    Description The trained observer and the staff supervising surgeon graded operative performance independently using a global rating scale, Global Operative Assessment of Laparoscopic Skills (GOALS) immediately after each case, (1 rating per case if bilateral repair). The GOALS tool has been shown to be a valid and reliable tool to measure generic laparoscopic skills in the simulated environment and in the operating room, with good agreement between live and video-review ratings. The scores range from 6 to 30, a higher score indicates greater operative performance.
    Time Frame at first TEP procedure post-randomization; due to surgical scheduling variability this can be anytime from 1 to 2 days following randomization to a week or two

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title Simulation Curriculum Current Practice
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice.
    Measure Participants 26 24
    Mean (Standard Deviation) [units on a scale]
    21.9
    (2.7)
    18.3
    (3.8)
    3. Secondary Outcome
    Title Number of Hernia Repair Subjects With Post-Operative Urinary Retention
    Description Urinary retention is the inability to empty the bladder. This is an educational study for surgeons. The participants in the study are surgeons, and the participant flow, baseline characteristics and first two outcome measures are for the surgeons. During the part of the study reported for the third outcome measure, the first surgical procedure (TEP) after randomization, each surgeon had one subject. Therefore, this outcome measure is for the hernia patients or subjects.
    Time Frame at first TEP procedure post-randomization, subjects were followed for the duration of hospital stay, an average of 1 night

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title Simulation Curriculum Current Practice
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice.
    Measure Participants 26 24
    Number [Subjects]
    0
    9

    Adverse Events

    Time Frame Adverse events were collected on all patients during the hernia operation and postoperative until release from the hospital for first hernia repair postrandomization.
    Adverse Event Reporting Description
    Arm/Group Title Simulation Curriculum Current Practice
    Arm/Group Description General surgery residents will undergo a simulation-based educational curriculum on totally extraperitoneal (TEP) hernia repair. General surgery residents will undergo training according to current practice.
    All Cause Mortality
    Simulation Curriculum Current Practice
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total / (NaN) / (NaN)
    Serious Adverse Events
    Simulation Curriculum Current Practice
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total 0/26 (0%) 0/24 (0%)
    Other (Not Including Serious) Adverse Events
    Simulation Curriculum Current Practice
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total 3/26 (11.5%) 24/24 (100%)
    Gastrointestinal disorders
    Epigastric vessel injury 1/26 (3.8%) 1 4/24 (16.7%) 4
    Musculoskeletal and connective tissue disorders
    Peritoneal tear 1/26 (3.8%) 1 9/24 (37.5%) 9
    Renal and urinary disorders
    Urinary Retention 0/26 (0%) 0 9/24 (37.5%) 9
    Skin and subcutaneous tissue disorders
    Hematoma 1/26 (3.8%) 1 2/24 (8.3%) 2
    Superficial skin infection 0/26 (0%) 0 2/24 (8.3%) 2

    Limitations/Caveats

    [Not Specified]

    More Information

    Certain Agreements

    All Principal Investigators ARE employed by the organization sponsoring the study.

    There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

    Results Point of Contact

    Name/Title Benjamin Zendejas, MD
    Organization Mayo Clinic
    Phone 507-538-5413
    Email zendejas.benjamin@mayo.edu
    Responsible Party:
    David R. Farley, PI, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT01085500
    Other Study ID Numbers:
    • 09-008118
    • 1UL1RR024150
    First Posted:
    Mar 12, 2010
    Last Update Posted:
    Oct 28, 2016
    Last Verified:
    Sep 1, 2016