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Surgical Ergonomics in OBGYN

Surgical Ergonomics in OBGYN Trainees & Attendings

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07609420
Enrollment
50
Registered
2026-05-27
Start date
2026-08-12
Completion date
2027-07-16
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Current OBGYN Attending, Resident, or Fellow at University Hospitals

Keywords

surgical ergonomics, obstetrics & gynecology, medical education

Brief summary

This is a voluntary research study to implement and assess the efficacy of interventions aimed to improve surgical ergonomics in OBGYN residents, fellows, and attendings and decrease the incidence of work-related musculoskeletal disorders (WRMD). We want to learn the baseline incidence of WMRD in our population and to see if the implementation of a surgical ergonomics lecture, pre-operative surgical ergonomics time-out, and intra-operative stretch breaks will improve the incidence of WRMD in this population.

Interventions

BEHAVIORALSurgical Ergonomics Lecture

60 min lecture regarding surgical ergonomics

BEHAVIORALPre-Incision Surgical Ergonomics Time Out

Pre-incision time-out (30-60s) focusing on surgical ergonomics in OR prior to starting a surgery

BEHAVIORALIntra-operative stretch breaks

30-60s breaks every 90 min to perform stretches during a surgical procedure

Sponsors

University Hospitals Cleveland Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

Current attending in the OBGYN department at University Hospitals Current resident or fellow in the OBGYN department at University Hospitals Participation in laparoscopic or open surgical procedures

Exclusion criteria

Not a current fellow, resident, or attending in the OBGYN department at University Hospitals

Design outcomes

Primary

MeasureTime frameDescription
Symptom frequency as measured by the Cornell Muscular Discomfort (MSK) Questionnaireweekly x 12 monthsSymptom frequency is measured on a likert scale of 0-4, with 0 being never and 4 being several times a day.
Symptom severity as measured by the Cornell Muscular Discomfort (MSK) Questionnaireweekly x 12 monthsSymptom severity is measured on a scale of 0-3, with 0 being slightly uncomfortable and 3 being very uncomfortable.
Work interference as measured by the Cornell Muscular Discomfort (MSK) Questionnaireweekly x 12 monthsWork interference is measured on a scale of 0-3, with 0 being not at all and 3 being substantially interfered.
Total Cornell Muscular Discomfort ScoresWeekly x 12 monthsFor each body region, a region-specific Cornell MSK discomfort score will be calculated as: Frequency × Severity × Work Interference. This yields a possible score range of 0-36 per body region.

Secondary

MeasureTime frameDescription
Incidence of work related musculoskeletal disorders (WRMDs)1 monthInitial incidence (presence or absence) of work related MSK disorders
Number of days of painkiller useweekly x 12 monthsMeasure of how many days per week a participant took over the counter medications (such as NSAIDs or tylenol) for musculoskeletal pain related to work. Scoring includes 0 days, 1-3 days, 4-5 days, daily

Countries

United States

Contacts

CONTACTAyesha Kar, MD
ayesha.karkasal@Uhhospitals.org2168441000
PRINCIPAL_INVESTIGATORAyesha Kar Kasal

University Hospitals Cleveland Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026