The Impact of Intraoperative Stretching Microbreaks on Otolaryngologists
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- George Washington University
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Body part discomfort
Study Overview
Brief Summary
There have been numerous survey-based and observational studies reporting a high percentage of otolaryngologists suffering from work-related musculoskeletal symptoms, in which more than half attributed to poor ergonomics in the operating room. Interventions have been implemented in the past to alleviate ergonomic hazards in general surgery such as intra-operative stretch breaks. However, there has not yet been an intervention done to alleviate ergonomic hazards in otolaryngologists. Our study aims to explore the efficacy of implementing intraoperative stretch breaks and assess their effect on otolaryngologists' practices and musculoskeletal pain.
Detailed Description
The study subjects will be recruited voluntarily from George Washington University Hospital otolaryngology attending physicians, residents, and fellows, as well as Children's otolaryngology faculties. Pre-survey will be sent prior to the intervention to obtain background information and baseline ergonomic assessment conducted by physical therapy students. Interventions will include intra-operative stretch breaks that will be implemented by surgeons at their convenient time during the surgery. Post-survey will be sent out to obtain the subjects' experiences after each intervention.
Each survey will be sent via email using a secured third-party vendor, RedCap. Results will be retrieved only by the research assistants listed on the institutional review board (IRB). The survey will not ask for any identifying information and will not publish identifying information. The raw data will be analyzed by the PI and research assistant for publication. The study should take less than a year for data collection and analysis.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 100 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Otolaryngologists
- •Currently practicing
Exclusion Criteria
- •Non-otolarynglogists
- •Currently not practicing
Arms & Interventions
Intervention group
Cross over study so each participant will have 3 control days without intervention and 3 intervention days with stretching exercise.
Intervention: Otolaryngology stretching micro-breaks (OSMB) (Behavioral)
Control group
Cross over study so each participant will have 3 control days without intervention and 3 intervention days with stretching exercise.
Outcomes
Primary Outcomes
Body part discomfort
Time Frame: Given after each surgery during intervention days
Body Part Discomfort is a validated survey with 0-5 score on the neck, shoulder R/L, hand R/L, lower/upper back, knee R/L, foot R/L. 0 with no pain to 5 with high pain.
Body part discomfort
Time Frame: Given before each surgery during control days as a baseline
Body Part Discomfort is a validated survey with 0-5 score on the neck, shoulder R/L, hand R/L, lower/upper back, knee R/L, foot R/L. 0 with no pain to 5 with high pain.
Body part discomfort
Time Frame: Given before each surgery during intervention days
Body Part Discomfort is a validated survey with 0-5 score on the neck, shoulder R/L, hand R/L, lower/upper back, knee R/L, foot R/L. 0 with no pain to 5 with high pain.
Body part discomfort
Time Frame: Given after each surgery during control days as a baseline
Body Part Discomfort is a validated survey with 0-5 score on the neck, shoulder R/L, hand R/L, lower/upper back, knee R/L, foot R/L. 0 with no pain to 5 with high pain.
Secondary Outcomes
No secondary outcomes reported
Investigators
Philip Zapanta
Associate professor
George Washington University