EMG Response in Forearm and Neck Muscles When Comparing Surgical Techniques.
NCT ID: NCT06978309
Last Updated: 2026-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
9 participants
OBSERVATIONAL
2025-05-06
2025-09-08
Brief Summary
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No study has compared the demands of RALS vs. LS on musculoskeletal fatigue (and subsequent injury risk). The investigators need to determine whether a career using RALS is associated with better musculoskeletal health of surgeons than standard LS when performing complex minimally invasive procedures.
The study will recruit Surgeons who perform prostate and bowel surgical procedures who have experience using RALS and/or LS. Surgeons will complete a series of validated questionnaires before and after each surgery to subjectively determine musculoskeletal strain/pain and will have body composition quantified.
They will be fitted with EMG (to measure muscle fatigue) whilst performing real-life surgery. Analysis of data gathered will be used to show what the short- and long- term musculoskeletal demands are and in turn determine if these are associated with changes in motor control.
The researcher's postulated hypothesis is that RALS should have less musculoskeletal effects both short and long term on surgeons, therefore, highlighting the fact that the implementation of RALS should be less controversial, because in the long run, the most expensive objects in the operating room are the personnel.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Robot-Assisted Laparoscopic Surgery
Surgeons performing robot assisted laparoscopic surgery.
No Interventions
Observational study.
Laparoscopic Surgery
Surgeons performing manual laparoscopic surgery.
No Interventions
Observational study.
Interventions
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No Interventions
Observational study.
Eligibility Criteria
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Inclusion Criteria
* Good musculoskeletal health.
* Adult.
Exclusion Criteria
* Significant co- morbidities that could affect the results of the study. Significant symptoms of musculoskeletal disorder.
* Anything the investigator feels will affect the study's measurements of safety.
18 Years
ALL
Yes
Sponsors
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Lancaster University
OTHER
Responsible Party
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Matthew Davitt
Principal Investigator
Locations
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Blackburn Royal Teaching Hospital
Blackburn, Lancashire, United Kingdom
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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FHM-2025-4948-IRAS-2
Identifier Type: -
Identifier Source: org_study_id
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