SOSII: SOS - Save Our Surgeons

Sponsor
University Hospital Tuebingen (Other)
Overall Status
Recruiting
CT.gov ID
NCT04352452
Collaborator
Institute of Occupational and Social Medicine and Health Services Research, Tuebingen (Other)
4
1
39
0.1

Study Details

Study Description

Brief Summary

Monocentric trial to evaluate differences in musculoskeletal and cognitive stress of robot-assisted laparoscopic surgery (RALS) vs. conventional laparoscopic surgery (CLS). Demographic and personal data are collected and pseudonymized as well as video recordings are performed during surgery. Simultaneously, surface electromyography (EMG) and electrocardiography (ECG), motion tracking data are collected. Additionally, saliva cortisol, perceived discomfort and mental load will be assessed within certain time intervals. The surgeon is not disturbed in his activity and movement by the equipment.

Afterwards, the surgeon will be interviewed in a 15-minute standardized interview about the surgery process and the subjective stress sensitivity. Only routine interventions will be recorded, in case of unforeseen complications, the recording will be stopped immediately

Condition or Disease Intervention/Treatment Phase
  • Procedure: laparoscopic surgery

Study Design

Study Type:
Observational
Anticipated Enrollment :
4 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
SOS - Save Our Surgeons - Differences in Musculoskeletal and Cognitive Stress of Robot-assisted Laparoscopic Surgery vs. Conventional Laparoscopic Surgery
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Apr 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
RALS

Surgeons perform robot-assisted laparoscopic surgery

Procedure: laparoscopic surgery
differences in musculoskeletal and cognitive stress

CLS

Surgeons perform conventional laparoscopic surgery

Procedure: laparoscopic surgery
differences in musculoskeletal and cognitive stress

Outcome Measures

Primary Outcome Measures

  1. Median muscular load of the bilateral trapezius pars descendens muscle surface electromyography. [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the 50th percentile the normalized RMS will be calculated [percent MVE]

  2. Static muscular load of the bilateral trapezius pars descendens muscle [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the 10th percentile of the normalized RMS [percent MVE] will be calculated.

  3. sustained muscular activity of the bilateral trapezius pars descendens muscle [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the number of episodes (≥ 8min) of the normalized RMS above 0.5percent MVE [n] will be calculated.

  4. Muscular rest time of the bilateral trapezius pars descendens muscle [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the frequency [n] and relative duration [percent] of the normalized RMS lower than 0.5percent MVE will be calculated.

Secondary Outcome Measures

  1. Median muscular load of the bilateral extensor digitorum and flexor carpi radials muscles [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the 50th percentile the normalized RMS will be calculated [percent MVE]

  2. Static muscular load of the bilateral extensor digitorum and flexor carpi radials muscles [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the 10th percentile of the normalized RMS [percentMVE] will be calculated.

  3. sustained muscular activity of the bilateral extensor digitorum and flexor carpi radials muscles [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the number of episodes (≥ 8min) of the normalized RMS above 0.5percent MVE [n] will be calculated.

  4. Muscular rest time of the bilateral extensor digitorum and flexor carpi radials muscles [75 Minutes]

    Muscle activity will be recorded using bipolar surface electromyography and is defined as the root-mean-square (RMS) of electrical muscle activity. Muscle activity will be normalized to an isometric voluntary maximum electrical activation (MVE) and the frequency [n] and relative duration [percent] of the normalized RMS lower than 0.5percent MVE will be calculated.

  5. Shoulder abduction angle [degree] [75 Minutes]

    Shoulder abduction angle will be assessed by the difference of two gravimetric position sensors placed on the upper back and the lateral side of the upper arm.

  6. trunk flexion angle [degree] [75 Minutes]

    Trunk flexion angle will be assessed by the difference of two gravimetric position sensors placed on the upper and lower back.

  7. head flexion angle [degreee] [75 Minutes]

    Head flexion angle will be assessed by the difference of two gravimetric position sensors placed on the upper back and the forehead.

  8. Frequency of perceived physical discomfort [n] [75 Minutes]

    Subjects will be asked in 20-min intervals throughout the surgery whether they feel any discomfort [yes or no]

  9. Intensity of perceived physical discomfort [0-10; 0 = nothing at all, 10 = extremely high [75 Minutes]

    Subjects will be asked in 20 -min intervals throughout the surgery about their level of perceived physical discomfort using a numeric rating scale [0 to 10].

  10. Subjective mental demand [0 - 21; 0 = very low, 21 = very high] [75 Minutes]

    Subjective mental demands will be assessed by the mental demand subscale of the NASA TLX questionnaire

  11. heart rate [beats per minute] [75 Minutes]

    Heart rate will be recorded by a one channel electrocardiogram

  12. Heart rate variability as the Standard Deviation of NN intervals [ms] [75 Minutes]

    Heart rate will be recorded by a one channel electrocardiogram and the standard Deviation of the NN interval will be calculated

  13. Heart rate variability as the Root Mean Squers of Successive Differences [ms] [75 Minutes]

    Heart rate will be recorded by a one channel electrocardiogram and the root mean square of the successive differences will be calculated

Other Outcome Measures

  1. Body height [cm] [5 Minutes]

    The Nordic Questionnaire will be used to determine subjects body height Physical activity [hours of sports per week work experience [years] musculoskeletal complaints in the last 12 month, last week, and point prevalence [n]

  2. Body weight [kg] [5 Minutes]

    The Nordic Questionnaire will be used to determine subjects body weight

  3. Physical activity [hours of sports per week] [5 Minutes]

    The Nordic Questionnaire will be used to determine subjects weekly physical activity

  4. work experience [years] [5 Minutes]

    The Nordic Questionnaire will be used to determine subjects work experience

  5. Musculoskeletal complaints in the last 12 month, last week, and point prevalence [n] [5 Minutes]

    The Nordic Questionnaire will be used to determine subjects musculoskeletal complaints in the last 12 month, last week, and point prevalence

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 68 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Age between 18 and 68 years

  • Able to work in full shift

  • trained surgeons in RALS and CLS

  • written informed consent

Exclusion Criteria:
  • persons influenced by analgesics or muscle relaxants

  • not being able to work for any reason

  • persons with acute diseases or pain Depending on the degree of severity, persons with diseases of the spine, hand-arm system, muscle disorders, symptomatic neurological-psychiatric disorders, when indicated regular medications, acute pain symptoms, diseases or other current illnesses must be excluded

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Tuebingen, Department of Women's Health Tuebingen Germany 72076

Sponsors and Collaborators

  • University Hospital Tuebingen
  • Institute of Occupational and Social Medicine and Health Services Research, Tuebingen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Tuebingen
ClinicalTrials.gov Identifier:
NCT04352452
Other Study ID Numbers:
  • MT_SOS II
First Posted:
Apr 20, 2020
Last Update Posted:
Jan 12, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 12, 2022