MinIAttention - Attention Management in Minimal Invasive Surgery

October 5, 2023 updated by: Klugsberger Bettina, Kepler University Hospital
Laparoscopic surgical suboptimal outcomes in patient safety measures are correlated with (i) cognitive load / level of attention of the operating surgeon, (ii) the frequency and degree of disruptions to the surgical workflow, and (iii) the misalignment of visual and motor axes in laparoscopic equipment / setting (eye-hand coordination).

Study Overview

Status

Completed

Detailed Description

Laparoscopic surgical suboptimal outcomes in patient safety measures are correlated with (i) cognitive load / level of attention of the operating surgeon, (ii) the frequency and degree of disruptions to the surgical workflow, and (iii) the misalignment of visual and motor axes in laparoscopic equipment / setting (eye-hand coordination).

This project will create the foundational, design and operational principles of future, surgeon-friendly minimal invasive surgery operating room information technologies (MIS-IT), which -given the ever growing complexity in surgical workflows, as well as instrument and equipment settings- will have to build on human attention as a scarce resource.

On the formal model's and methods' side, MinIAttention will identify types of human attention, as well as cognitive and physiological mechanisms revealing its relation to perception, memory, decision making, and learning. Starting with established theories of individual attention (Capacity Theory, Multiple Resource Theory, Feature Integration Theory) and the respective attention models (Broadbent, Kahneman, Wickens), the investigators will characterize aspects of attention of surgeons during MIS operations. MinIAttention will empirically evidence its models on the dynamics of a surgeon's attention along the workflow of a MIS operation. A multi-sensor attention recognition reference framework will be implementation, involving externalized signals of a surgeons attention (eye gaze, head and hand gesture, head and full body pose, physiological signals, as well as communication and social interaction). Evidenced MinIAttention attention models will represent the core body of aware surgeon assistance systems, covering (i) sensory assistance, enhancing the surgeons perceptual capacities, (ii) motor assistance, enhancing the surgeons motor and manipulative capacities (iii) decision making assistance, guiding the surgeon towards informed, evidence based, rational, transparent and timely decisions during operation, and (iv) cognitive assistance, enhancing the surgeons memory management capacities with background digital memory systems. On the purpose of supporting this research proposal with an early impression of the feasibility of the proposed research method and approach, the proposing partners have voluntarily set up prototypical attention capturing system. With this preliminary proposal support study the investigators have evidenced that ensembles of sensors together with our attention models can serve as a nonobtrusive, yet potentially effective means to determine indicators of a surgeon's attention during live surgeries. Above that, the pattern recognition methods an machine learning techniques appear viable for the task of automated attention and cognitive load diagnosis, and the proposed assistance and mulitmodal feedback system reveals feasible. The investigators can thus say, that the research method and approach which MinIAttention will build upon is solid, promising, and preliminarily evidenced beforehand.

Aside the MIS-IT focus of this project, MinIAttention will serve as a reference to a very general, observably upcoming information society dilemma: information overload and attention scarcity. In today's information-rich world, where people are overflooded with signals and messages at all levels of perception and modalities (visual, auditory, tactile, olfactory), the need to allocate attention efficiently among the overabundance of information sources appears to be among the most demanding challenges for ICT mediated communication today. For the design and implementation of novel, future ICT systems of all kinds, it is of high interest to understand how spontaneous, local, individual attention to novel information items occurs. Some two decades of HCI and pervasive/ubiquitous computing research have clearly revealed that out of the many indicative design factors for modern ICT, human attention is the first source of perception, consequently also awareness towards information and other individuals. MinIAttention will create the foundational basis for attention-aware ICT, i.e. develop (i) formal models of human attention along with (ii) multisensory recognition architectures and reasoning algorithms to estimate and assess levels of human attention, together with their (iii) embedding into ICT systems of everyday use.

Five international groups will collaborate to develop MinIAttention. JKU IPC has introduced attention aware ICT in the Pervasive Computing scientific community, developed pionieering methods and systems, and also promoted cognitive ICT to become a European research priority (H2020). AKH KUK runs Austrias most advanced laparoscopic operation theater with cutting edge technological equipment, Karl STORZ ENDOSKOPE is a worldwide leading surgical instrument supplier. SUSSEX is among the worlds most renowned institutions in machine learning related to wearable computing, as is FRI for vital state recognition.

Study Type

Observational

Enrollment (Actual)

42

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Upper Austria
      • Linz, Upper Austria, Austria, 4020
        • Kepler University Clinic

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

surgeons for General and Visceral surgery

Description

Inclusion Criteria:

  • laparoscopic cholecystectomy

Exclusion Criteria:

  • open surgical procedures

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
surgeon´s attention
Time Frame: july 2017 until December 2019
surgeon´s attention during laparoscopic surgery
july 2017 until December 2019

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 6, 2016

Primary Completion (Actual)

January 30, 2019

Study Completion (Actual)

December 30, 2020

Study Registration Dates

First Submitted

November 30, 2017

First Submitted That Met QC Criteria

November 30, 2017

First Posted (Actual)

December 6, 2017

Study Record Updates

Last Update Posted (Estimated)

October 9, 2023

Last Update Submitted That Met QC Criteria

October 5, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Minatt-017

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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