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Behav'Robot: Understanding the Surgeon Behavior During Robot-assisted Surgery

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ClinicalTrials.gov Identifier: NCT04869995
Recruitment Status : Not yet recruiting
First Posted : May 3, 2021
Last Update Posted : May 3, 2021
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier de Troyes

Study Description
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Brief Summary:

Robot-assisted surgery is spreading since the last decade, but little is known about the impact of the use of the robot on surgeon practices and behavior in the operation theatre.

Interviewing senior surgeons trained for doing robot-assisted surgery, this qualitative study is expected to provide new insights to understand the surgeons' behavioral changes when using a robot.

This study will contribute to improving training programs in robot-assisted surgery.


Condition or disease Intervention/treatment
Robotic Surgical Procedures Other: Interview

Study Design
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Study Type : Observational
Estimated Enrollment : 20 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Behav'Robot: Understanding the Surgeon Behavior During Robot-assisted Surgery (a Qualitative Study)
Estimated Study Start Date : May 15, 2021
Estimated Primary Completion Date : July 31, 2021
Estimated Study Completion Date : July 31, 2021
Groups and Cohorts
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Group/Cohort Intervention/treatment
Intervention
Senior abdominal and pelvic cavity surgeons (i.e., visceral surgeons, gynecologist surgeons, and urologists) having completed their robot-assisted surgery training, and commonly doing laparoscopic surgery.
 Other: Interview
An individual semi-structured interview per surgeon, according to an interview guide.


Outcome Measures
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Primary Outcome Measures :
  1. Elicitation of the surgeons' perception [ Time Frame: = interview duration (about 30 minutes) ]
    Elicitation of the surgeons' perception of practices and behavior changes when doing robot-assisted surgery.


Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Study participants will comprise senior abdominal and pelvic cavity surgeons (i.e., visceral surgeons, gynecologist surgeons, and urologists) having completed their robot-assisted surgery training, and commonly doing laparoscopic surgery.
Criteria

Inclusion Criteria:

  • Senior abdominal and pelvic cavity surgeons (i.e., visceral surgeons, gynecologist surgeons, or urologists).
  • Having completed a robot-assisted training
  • Commonly doing laparoscopic surgery

Exclusion Criteria:

  • Those who refuse to participate in the study
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04869995


Contacts
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Contact: Stéphane Sanchez, MD +33 6 25 03 68 92 stephane.sanchez@hcs-sante.fr

Sponsors and Collaborators
Centre Hospitalier de Troyes
More Information
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Responsible Party: Centre Hospitalier de Troyes
ClinicalTrials.gov Identifier: NCT04869995    
Other Study ID Numbers: BehavRobot
First Posted: May 3, 2021    Key Record Dates
Last Update Posted: May 3, 2021
Last Verified: April 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No