EffectS of prEferred Music on Laparoscopic performancE (EnSEMbLE)

November 5, 2019 updated by: Prof. dr. Gert-Jan Kleinrensink, Erasmus Medical Center

The Effect of Preferred Music on Laparoscopic Performance

The main objective is to investigate whether listening to recorded music has a positive effect on the execution of laparoscopic skills.

Secondary objectives are to investigate the effects of music during surgical performance on blood pressure, mental workload and heart rate.

Study design: This will be a 4-period 4-sequence 2-treatment crossover study, participants will be exposed to both control (noise cancelling headphones without music) and the intervention (preferred music via headphones) whilst performing a laparoscopic task in a box trainer. Every period consists of 5 repetitions of a laparoscopic peg transfer task. In total participants will perform in each condition 10 peg transfer tasks.

Prior to the experiment, all participants practice the laparoscopic peg transfer task 20 times

Study population: Healthy volunteering medicine students without laparoscopic experience.

Intervention (if applicable): Participants will perform 2 periods of 5 laparoscopic peg transfer task whilst listening to preferred recorded music via headphones and 2 periods of 5 laparoscopic peg transfer tasks while wearing noise cancelling headphones without music (2 periods of 5 tasks).

Main study parameters/endpoints: The primary endpoint is laparoscopic performance as defined by time of task completion Secondary endpoints are: laparoscopic task performance (path length, jerk, error score, economy of motion) vital parameters (heart rate, and post test blood pressure) and mental workload (SURG-TLX)

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

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

    • Zuid-Holland
      • Rotterdam, Zuid-Holland, Netherlands, 3015 GD
        • Erasmus MC

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

In order to be eligible to participate in this study a subject must meet all of the following criteria.

  • Age ≥ 18 years
  • Medicine students
  • Provision of written informed consent by the subject.

A potential subject who meets any of the following criteria will be excluded from participation in this study:

  • Severe hearing impairment, defined as no verbal communication possible.
  • Severe visual impairment, defined as not able to see the monitor on which the laparoscopic task is projected.
  • Any physical handicap that impairs laparoscopic performance (unable to stand for 10 minutes, unable to hold and use both instruments.

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

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Music
During laparoscopic task performance; participants will wear a noise cancelling headphone that plays music that is chosen by the participant.
Participant selected music, applied using noise cancelling headphones
No Intervention: No music
During laparoscopic task performance; participants will wear a noise cancelling headphone that does not play music.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time to task completion (s)
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total

It will be measured in seconds and calculated using data generated from motion analysis software. Each tasks starts, when the participants puts the tip of the grasper in a yellow square that is projected on the screen, after task completion the participant puts tip in the square again to finish the task. The time between start and finish is defined as the time to task completion.

An average is calculated for both the 10 tasks in the intervention group and the 10 tasks in the control group.

This will be measured during the experimental session which will take up about 1 hour in total

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Path length
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total
The total distance the tip of the instrument has travelled per task (mm) per task, it will be calculated using data generated from motion analysis software. Each tasks starts, when the participants puts the tip of the grasper in a yellow square that is projected on the screen, after task completion the participant puts tip in the square again to finish the task. An average is calculated for both the 10 tasks in the intervention group and the 10 tasks in the control group.
This will be measured during the experimental session which will take up about 1 hour in total
Normalized jerk
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total
the rate of change of acceleration of the instrument tips (m/s3) per task. It will be calculated using data generated from motion analysis software. Each tasks starts, when the participants puts the tip of the grasper in a yellow square that is projected on the screen, after task completion the participant puts tip in the square again to finish the task. An average is calculated for both the 10 tasks in the intervention group and the 10 tasks in the control group.
This will be measured during the experimental session which will take up about 1 hour in total
Mental workload
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total

Mental workload will be assessed using the Surgery task load index (SURG-TLX) this is a validated multidimensional, surgery-specific workload measure. The SURG-TLX is an adapted version of the National Aeronautics and Space Administration Task Load Index (NASA-TLX).

In the SURG-TLX subjects rate six dimensions of workload i.e. situational stress, distractions, task complexity, physical demands, temporal demands and mental demands on visual analogue scales VAS ranging from 0-100 (0 = very low;100 = very high) the scores of these subscales are combined into a weighed average that results in a general score ranging from 0-100 (0 = very low; 100 = very high) After every period of 5 tasks a SURG-TLX questionnaire is completed. An average is calculated for both the two periods in the intervention group and the two periods in the control group. The averages of both the general score and the individual subscales will be reported.

This will be measured during the experimental session which will take up about 1 hour in total
Heart rate
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total
Heart rate will be assessed prior to; and immediately after every period of laparoscopic tasks in beats per minute. Change in heart rate before and after each period of tasks is calculated. An average change will be calculated for both the two periods in the intervention group and the two periods in the control group
This will be measured during the experimental session which will take up about 1 hour in total
Blood pressure
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total
Systolic and diastolic pressure will be assessed prior to and immediately after every period of laparoscopic tasks in mmHg. Change in blood pressure before and after each period of tasks is calculated. An average change will be calculated for both the two periods in the intervention group and the two periods in the control group
This will be measured during the experimental session which will take up about 1 hour in total
Participant's characteristics
Time Frame: This will be measured during the experimental session which will take up about 1 hour in total
  • Age (years)
  • Sex (male or female)
  • Dexterity (left- or right handed, ambidextrous)
  • Year of medical education:
  • The importance of music in daily life on a (10-point numeric rating scale)
  • Musical genres the subject listens to (classical, world music, rock, pop, techno, house, jazz, blues, disco, other)
  • Musical genres the subject listens to when studying: (classical, world music, rock, pop, techno, house, jazz, blues, disco, other)
  • choice of music during the experiment
  • Whether or not the subject plays or has played a musical instrument (never, in the past, currently)
  • Whether or not the subject plays or has played video games and to what extends (never, in the past, currently)

This questionnaire will be completed before starting the practice session of 20 laparoscopic tasks.

This will be measured during the experimental session which will take up about 1 hour in total

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Gert-Jan Kleinrensink, Prof. Dr., Erasmus MC

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)

June 1, 2018

Primary Completion (Actual)

November 30, 2018

Study Completion (Actual)

November 30, 2018

Study Registration Dates

First Submitted

September 4, 2019

First Submitted That Met QC Criteria

September 30, 2019

First Posted (Actual)

October 1, 2019

Study Record Updates

Last Update Posted (Actual)

November 7, 2019

Last Update Submitted That Met QC Criteria

November 5, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • MEC-2018-1134

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

product manufactured in and exported from the U.S.

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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