Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT04748549

Intraoperative VR for Older Patients Undergoing TKA

Led by Beth Israel Deaconess Medical Center · Updated on 2025-06-04

131

Participants Needed

1

Research Sites

298 weeks

Total Duration

On this page

Sponsors

B

Beth Israel Deaconess Medical Center

Lead Sponsor

I

Israel-United States Binational Industrial Research and Development Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of this study is to investigate whether the use of virtual reality (VR) during total knee arthroplasty (TKA) can facilitate reductions in intraoperative sedative requirements while maintaining high levels of patient satisfaction as compared to both a music and sham VR + usual care control.

CONDITIONS

Official Title

Intraoperative VR for Older Patients Undergoing TKA

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients age 60 or older undergoing primary total knee replacement surgery at BIDMC and receiving spinal/regional anesthesia
  • English or Spanish speaking patients
Not Eligible

You will not qualify if you...

  • Complex or revision surgeries
  • Patients scheduled for "same day" TKA
  • Open wounds or active infection of the face or eye area
  • History of seizures or other symptom linked to an epileptic condition
  • Patients who plan to wear hearing aids during the procedure
  • Patients with a pacemaker or other implanted medical device
  • Droplet or airborne precautions (as determined by local infection control policy)
  • Non-English speaking or Non-Spanish speaking
  • Moderate to severe dementia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

B

Brian P O'Gara, MD,MPH

CONTACT

A

Anna Fratello, B.S.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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