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The Effect of Intelligent Exercise and Ergonomic Recommendations on Surgeon Musculoskeletal Discomfort

Not Applicable
Recruiting
Conditions
Occupational Exposure
Occupational Injuries
Interventions
Behavioral: Intelligent Physical Exercise Training (IPET)
Registration Number
NCT06112106
Lead Sponsor
University of Aarhus
Brief Summary

The goal of this clinical trial is to investigate the effects of Intelligent Physical Exercise Training (IPET) and ergonomic recommendations on musculoskeletal pain among abdominal and pelvic surgeons. The main question it aims to answer is:

• Is IPET superior to ergonomic recommendations in rehabilitating or preventing musculoskeletal pain?

12 weeks ahead of trial start, all participants will be familiarized with ergonomic principles in the operating room. In the 20-week trial, the control group is asked to resume practicing and applying the ergonomic principles when they operate. In addition to applying the ergonomic principles, the Intervention group will be asked to perform 50 min. per week of individually tailored physical exercise training. The program is delivered via an application (app).

Detailed Description

Pre-intervention The three months leading up to the trial start, all participants are introduced to up-to-date ergonomic recommendations. The ergonomic recommendations are informed by general ergonomic recommendations from the Danish Working Environment Authority, a systematic literature review on the effect of ergonomic interventions applied in the OR (REF and general ergonomic guidelines) and include two recommendations: 1) performing intra-operative microbreaks, and 2) knowledge of ergonomic work posture in the OR.

InterventionIntelligent Exercise app + ergonomic recommendations The duration of the ergonomic recommendations launch period is three months after which consenting participants will be randomized to either the control group or the intervention group. The control group will be encouraged to continue to apply the up-to-date ergonomic recommendations to their OR practice, this will act as usual care. In addition to the usual care, the intervention group will be prescribed individualized physical exercise training (IPET). The IPET is 50 min of tailored physical exercise per week, that is designed by an algorithm that uses the information (demographics, self-reported health, musculoskeletal pain and its location) the individual enters in the app (REF). The 50 min. Of total IPET per week can be performed in one session or divided into shorter sessions two-five sessions with the same effect (REF). The IPET will be delivered through the participants' mobile phone via a mobile application (app) that requires a unique code assigned for each participant. Each participant's exercise training program is different because it is composed of the input provided by the participant. Thus, as the participants experience progress (or deterioration) in their physical capacity during the study, the program will change accordingly.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
170
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupIntelligent Physical Exercise Training (IPET)Surgeons
Primary Outcome Measures
NameTimeMethod
Musculoskeletal pain intensityAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Pain intensity on a 11-point Likert scale (0= no pain, 10= most intense pain) the past 3 months and last 7 days in neck, shoulders, elbows/arms, wrists/hands, upper back, lower back, hips, knees, ankle/feet

Secondary Outcome Measures
NameTimeMethod
Self-reported use of pain medicineAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Use of pain medicine due to musculoskeletal pain. Answer categories: daily, one to several times a week, one to several times a month, rarely or never

Self-reported time spent on moderate to vigorous physical activity during a regular week (in minutes)Assessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Accumulated physical activity during a regular week (hours/minutes). Answer categories for moderate physical activity: less than 30 min., 30-90 min., 90-149 min., 150-299 min., 300 min. or more. Answer categories for vigorous physical activity: less than 30 min, 30-89 min, 90-149 min, 150 min. or more.

Self-reported physical resourcesAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Rating own physical resources (cardiorespiratory fitness, strength, balance) compared to peers on a Likert scale (0= poor, 10= good).

Self-reported healthAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

General health answer categories: On a five-point Likert scale (0= excellent, 5= poor). Physical and mental health rated on various likert scales.

Self-reported personal and work-related burnoutAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

The Copenhagen Burnout Inventory. Answer categories: 5-point Likert scales from "always" to "almost never or never", or from "very much" to "very little"

Working conditionsAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Surgical specialty, weekly workings hours as primary and assisting surgeon

Self-reported work abilityAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

The Work Ability Index (WAI) contains questions concerning work, work ability and health.

Musculoskeletal pain frequency past 3 monthsAssessed at baseline (pre-intervention), 12 weeks and 20 weeks (post-intervention)

Pain frequency for the past 3 months (possible answers: 0d, 1 to 7d, 8 to 30d, more than 30 days but not every day, every day)

Trial Locations

Locations (1)

Aarhus University

🇩🇰

Aarhus, Denmark

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