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Behavioural Intervention

Surgical Ergonomics Education for Preventing Work Injuries (SEE MIGS Trial)

N/A
Recruiting
Led By Kari Plewniak, MD
Research Sponsored by Montefiore Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from enrollment during session 1 until conclusion of study in session 2, approximately 8 weeks total
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to see if teaching obstetrics and gynecology doctors about ergonomic body positions and having them practice these positions will help prevent injuries at work. Participants will attend a class and then be divided

Who is the study for?
This trial is for obstetrics and gynecology doctors in training. It's designed to see if a class on ergonomic body positions, combined with hands-on practice, can help them learn to move in ways that prevent work-related injuries.
What is being tested?
The study tests whether ergonomics education and guided practice improve how these doctors position their bodies during surgery. One group gets both the class and feedback-driven practice; another only attends the class. Their skills are videotaped and compared over time.
What are the potential side effects?
Since this trial involves educational interventions rather than medical or drug treatments, traditional side effects aren't expected. However, participants may experience fatigue or muscle strain from practicing surgical skills.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from enrollment during session 1 until conclusion of study in session 2, approximately 8 weeks total
This trial's timeline: 3 weeks for screening, Varies for treatment, and from enrollment during session 1 until conclusion of study in session 2, approximately 8 weeks total for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change from baseline in surgical ergonomic knowledge score over two sessions
Change from baseline in surgical ergonomic practice based on rapid entire body assessment (REBA) score over two sessions
Change from baseline in surgical ergonomic practice based on rapid upper limb assessment (RULA) score over two sessions
+3 more
Secondary study objectives
Number of participants that reported an increase in knowledge following surgical ergonomics lecture/module and/or skills practice.
Number of participants that reported an increase in practice following surgical ergonomics lecture/module and/or skills practice.
Number of participants that reported that surgical ergonomics education is valuable following surgical ergonomics lecture/module and/or skills practice
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Intervention groupExperimental Treatment2 Interventions
This group will receive directed feedback and guided practice regarding their ergonomic positioning while performing basic surgical skills exercises on a trainer
Group II: ControlExperimental Treatment1 Intervention
This group will not receive directed feedback or guided practice regarding their ergonomic positioning while performing basic surgical skills exercises on a trainer during the study. After the study is completed they will receive this feedback, but it will not be included as a part of the study data.

Find a Location

Who is running the clinical trial?

Montefiore Medical CenterLead Sponsor
456 Previous Clinical Trials
588,446 Total Patients Enrolled
Kari Plewniak, MDPrincipal InvestigatorMontefiore Medical Center
~16 spots leftby Jan 2025