Evaluating the impact of intraoperative exercises on gynecologic surgeons' pain
Microbreaks and Intraoperative Exercises for Gynecologic Surgeons (MIGS Trial)
This study is testing whether taking short exercise breaks during surgery can help gynecologic surgeons feel less pain and discomfort while they work.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Sex | All |
| Sponsor | University of Texas at Austin Academic / other |
| Locations | 1 site (Austin, Texas) |
| Trial ID | NCT05761288 on ClinicalTrials.gov |
What this trial studies
This study aims to assess the effectiveness of intraoperative microbreaks and exercises in reducing body discomfort among gynecologic surgeons. It involves a randomized trial where participating surgeons will alternate between surgery days with and without these microbreaks and exercises. Eligible participants include residents, fellows, and attending surgeons who perform gynecologic surgeries regularly. Data will be collected through questionnaires to evaluate musculoskeletal symptoms and other relevant factors.
Who should consider this trial
Good fit: Ideal candidates for this study are gynecologic surgeons, including residents, fellows, and attendings, who perform surgeries at least two days per month.
Not a fit: Surgeons who are unable to perform the exercises or do not meet the surgical frequency criteria may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce musculoskeletal pain for gynecologic surgeons, enhancing their well-being and potentially improving surgical performance.
How similar studies have performed: While the specific approach of intraoperative exercises is novel, similar studies have shown that microbreaks can improve physical well-being in other surgical specialties.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Residents, fellows, and attendings performing gynecologic surgery (including benign gynecologists, gynecologic oncologists, minimally invasive gynecologists, and urogynecologists) who are able to perform the exercises. * Surgery days must contain at least one gynecologic surgery with two hours of total operating time in one day. * Surgeons will need to have operated on average at least 2 days per month over the last 12 months. Exclusion Criteria: * Participants will be excluded if they are unable to perform the exercises.
Where this trial is running
Austin, Texas
- The University of Texas at Austin — Austin, Texas, United States (Recruiting)
Study contacts
- Study coordinator: Laura M Kent, MD
- Email: mkent.laura@gmail.com
- Phone: 4044887778
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.