- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04111679
EffectS of prEferred Music on Laparoscopic performancE (EnSEMbLE)
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
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Zuid-Holland
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Rotterdam, Zuid-Holland, Netherlands, 3015 GD
- Erasmus MC
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
|
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
Sponsor
Investigators
- Principal Investigator: Gert-Jan Kleinrensink, Prof. Dr., Erasmus MC
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MEC-2018-1134
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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