Resident Posture Biofeedback Study

Wake Forest University (WFU)

Status: Completed

Conditions: Healthy; Postural; Strain

Treatments: Device: Posture Biofeedback Device

Study type: Interventional

Funder types: Other

Identifiers

NCT06564519

IRB00115419

Details and patient eligibility

About

While a majority of surgical ergonomic studies have been evaluating attending surgeons, few have evaluated surgical ergonomics within the surgical resident. Biofeedback devices can be partnered with education and geared towards surgical residents to decrease current and future musculoskeletal disorders, which may in turn lead to longer and more fulfilling careers.

Full description

This study aims to use a commercially-available posture training device for surgical residents that sends biofeedback in the form of a gentle vibration if posture has deviated from the upright (neutral) position for a long period of time. For residents performing minimally-invasive procedures with a laparoscopic approach, our overarching hypothesis is that the time spent in a non-upright position will be less after using the posture biofeedback device compared with before. The study hypothesizes that residents will report fewer complaints related to musculoskeletal pain after wearing the posture training device.

Residents completing general surgery rotations will be recruited and wear a biofeedback device for about four weeks while performing laparoscopic procedures. Posture data from the device and survey data in the form of the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ) will be collected and analyzed.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Surgical residents with surgical experience of at least one year (Postgraduate year 2-5)
• Completing a one-month rotation at the study sites within the general surgery department during the study period

Exclusion criteria

• Clinically diagnosed inflammatory musculoskeletal disorders per self-report
• History of orthopedic surgery in the last six months per self-report

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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12 participants in 1 patient group

Residents

Other group

Description:

This is a single arm study. All Resident participants will use the posture biofeedback device.

Treatment:

Device: Posture Biofeedback Device