Actively Recruiting
Virtual Reality and Standard Care vs. Standard Care Alone for Acute MSK Pain in Geriatric ED Patients
Led by Antonios Likourezos · Updated on 2026-01-16
180
Participants Needed
1
Research Sites
162 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The proposed Virtual Reality as an Adjunct to Pain Management for Geriatric Patients in the ED (VRAP-ED) project will take place in the Emergency Medicine Department at Maimonides Medical Center. It seeks to enhance the analgesic practices for geriatric patients with acute painful conditions in the emergency setting. Although virtual reality (VR) has demonstrated effectiveness in reducing pain and anxiety in various clinical settings for juveniles and adults, the analgesic efficacy of VR for geriatric ED patients lacks established data. The project will use a geriatric-focused VR platform. The project intends to improve pain management for almost 200 geriatric patients by evaluating the effectiveness of virtual reality (VR) in reducing pain and its impact on anxiety \& stress reduction. The research project will conduct a randomized clinical trial to investigate the analgesic efficacy and impact on anxiety \& stress by using VR as an adjunct to the standard of care (SOC) for pain management in elderly patients presenting to the ED with acute musculoskeletal pain. This will be investigated through a prospective, randomized, non-blinded clinical trial conducted over two years. Eligible patients will be randomly assigned to either the control (SOC) or intervention (SOC+VR) groups. The expected outcomes of this research study will provide insight into the feasibility of using VR in a busy emergency setting for one of the most commonly encountered painful syndromes and to assess the analgesic efficacy as well as the satisfaction of VR application by both patients and ED clinicians.
CONDITIONS
Official Title
Virtual Reality and Standard Care vs. Standard Care Alone for Acute MSK Pain in Geriatric ED Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 65 years or older
- Emergency Medicine patients
- Non-traumatic musculoskeletal painful condition
- Pain score of 4 or higher on a numeric rating scale
- Patient requires parenteral analgesia as determined by treating physician
- Patient must be awake, alert, and oriented to person, place, and time
- Ability to understand informed consent and study-related information
- Ability to complete assessments
You will not qualify if you...
- Painful syndrome requiring emergent or urgent pain control
- Altered mental status
- Unstable vital signs
- History of recent epilepsy
- Seizure disorder
- Vertigo
- Active headache
- Nausea
- Motion sickness
- Dizziness
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Maimonides Medical Center
Brooklyn, New York, United States, 11219
Actively Recruiting
Research Team
S
Sergey Motov, MD
CONTACT
A
Antonios Likourezos, MA, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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