Physiatrist Ergonomic Intervention on Work Related Musculoskeletal Pain in Surgeons

Sponsor
University of Texas Southwestern Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05946018
Collaborator
(none)
50
2
16

Study Details

Study Description

Brief Summary

The goal of this randomized control trial is to learn if physical therapy coaching and education improves work-related muscle pain in surgeons more than education alone. The main focuses of this study are to:

  1. To evaluate pain in surgeons before and after surgical cases.

  2. To evaluate work-load related stress in surgeons after surgical cases.

  3. To evaluate surgeons' quality of life.

  4. To evaluate surgeons' grip strength.

Participants will be put into two groups at random. One group will watch an educational video only. The other group will watch an educational video and get a coaching session from a physical therapist.

Condition or Disease Intervention/Treatment Phase
  • Other: Educational video on ergonomics
  • Other: Verbal physical therapy coaching sessions
N/A

Detailed Description

All participants will undergo the same baseline, pre-intervention assessments. Pre-intervention assessments will include several questionnaires: general demographic and baseline questionnaire, WHO GPAQ for assessment of physical activity, non-fatigued baseline grip assessment. Additionally, following one day operating they will complete a fatigued grip assessment, SURG-TLX questionnaire, Brief Pain Index (BPI), and a questionnaire regarding how many hours they operated that day and what type of surgeries they performed (Surgery Day Questionnaire).

For participants randomized to the education only group, they will watch a short (5-7 minute) educational video. The video content includes information on why ergonomics is important (preventing work-related musculoskeletal disorders, types of injuries, physician longevity) and recommendations for how to ergonomically arrange the operating room to reduce the risk of injury.

For participants randomized to the education plus personal coaching group, they will first watch the same video as described previously. Then they will have four 15 to 20-minute sessions with a physiatrist. These sessions will include a standard assessment with individualized instruction on range of motion, strength, endurance, and flexibility. These sessions will include verbal coaching, instructor demonstration, however no hands-on treatment or intervention will be provided. The sessions will occur at 0 weeks (same day as participant views video), 2 weeks, 4 weeks, and 6 weeks after viewing of the educational video. The first session will be in person, the remainder of the sessions will be virtual.

Post-intervention follow up will begin after the video is viewed by those in the education-only group and after the video is viewed and the first personal coaching session is complete by the education plus coaching group. The first timepoint of post-intervention assessment will be the first operating day after the intervention. Assessments will include grip assessment, SURG-TLX, BPI, and Surgery Day Questionnaire. Two additional post-intervention assessments will be at 2 weeks after initial intervention and 6 weeks after initial intervention. The 6 week timepoint reflects the completion of the personal coaching series for those in that group.

Long-term follow-up assessments will be performed at 3 and 6 months after the initial intervention (week 0). The assessments that will be administered then will include a demographic/general questionnaire, WHO GPAQ, grip assessment (non-fatigued and fatigued), SURG-TLX, BPI, and Surgery Day Questionnaire. All questionnaires and assessments (including grip strength) will be administered in-person by a study member to the participant.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Physiatrist Ergonomic Intervention on Work Related Musculoskeletal Pain in Surgeons: A Randomized Control Trial
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Education only

This arm only includes a 6-8 minute educational video on ergonomics.

Other: Educational video on ergonomics
A 6-8 minute education video that includes information on why ergonomics is important and recommendations for how to arrange the operating room to reduce the risk of injury.

Other: Education and coaching sessions

This arm includes a 6-8 minute education video on ergonomics and 1:1 15 minute coach sessions at 0, 2, 4, and 6 weeks.

Other: Educational video on ergonomics
A 6-8 minute education video that includes information on why ergonomics is important and recommendations for how to arrange the operating room to reduce the risk of injury.

Other: Verbal physical therapy coaching sessions
Physical therapy coaching sessions include a standard assessment with individualized instruction on range of motion, strength, endurance, and flexibility.

Outcome Measures

Primary Outcome Measures

  1. To evaluate pain in surgeons after operating. [6 months]

    Surgeons receiving personalized education and a physical activity plan will report less pain (as assessed by the Brief Pain Index). The BPI measures pain on a 0-10 scale with higher scores meaning worse outcomes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Attending/faculty surgeon or surgical trainee (PGY2 or above) in any surgical specialty

  • Operates at least one day per week

Exclusion Criteria:
  • Currently under active treatment for a musculoskeletal injury (example: physical therapy)

  • Plans to decrease operating time to less than one day per week in the next 6 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Texas Southwestern Medical Center

Investigators

  • Principal Investigator: Kimberly Kho, MD, UTSW

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kimberly Kho, MD, University of Texas Southwestern Medical Center
ClinicalTrials.gov Identifier:
NCT05946018
Other Study ID Numbers:
  • STU-2023-0516
First Posted:
Jul 14, 2023
Last Update Posted:
Jul 17, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 17, 2023