Investigating exercise and ergonomic recommendations for surgeon pain relief
A Multi-center, Randomized, Parallel-group, 4-month Study to Compare the Effect of Ergonomic Recommendations Versus Intelligent Physical Exercise Training (IPET) and Ergonomic Recommendations on Musculoskeletal Pain Among Abdominal and Pelvic Surgeons.
This study is testing whether a new exercise program combined with ergonomic tips can help abdominal and pelvic surgeons feel less pain in their muscles and joints.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 170 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Aarhus Academic / other |
| Locations | 1 site (Aarhus) |
| Trial ID | NCT06112106 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of Intelligent Physical Exercise Training (IPET) compared to standard ergonomic recommendations in reducing musculoskeletal discomfort among abdominal and pelvic surgeons. Participants will first receive training on ergonomic principles for three months, after which they will be randomized into a control group, which continues with ergonomic practices, or an intervention group that also engages in tailored physical exercise training delivered via a mobile app. The trial spans 20 weeks, focusing on the rehabilitation and prevention of pain through these interventions.
Who should consider this trial
Good fit: Ideal candidates for this study are surgeons specializing in gynecologic, urologic, colorectal, or abdominal surgery who perform an average of four hours of surgery per week.
Not a fit: Patients who have been advised against physical exercise training by their physician will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce musculoskeletal pain among surgeons, improving their quality of life and work performance.
How similar studies have performed: Other studies have shown promising results with ergonomic interventions and exercise programs in reducing occupational injuries, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Surgeon in gynecologic-, urologic, colorectal or abdominal surgery * Performs an average of four hours of surgery per week Exclusion Criteria: * Own physician has advised against performing physical exercise training
Where this trial is running
Aarhus
- Aarhus University — Aarhus, Denmark (Recruiting)
Study contacts
- Principal investigator: Helle J Christiansen, Msc. — University of Aarhus
- Study coordinator: Helle J Christiansen, Msc.
- Email: hjchristiansen@clin.au.dk
- Phone: +4550176163
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.