Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT03987334

Virtual Reality Rehabilitation in Neck Pain Subjects

Led by IRCCS San Raffaele · Updated on 2026-02-23

72

Participants Needed

1

Research Sites

464 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

VR-NECKPAIN is a two-arm, monocentric, single-blind, randomized controlled trial in Neck Pain patients. The entire treatment consist in 12 sessions, each during 45 minutes, twice a week for 6 consecutive weeks. Subjects will be evaluated ad baseline (T0) and after six weeks of rehabilitation (T1). There will also be a 3 months Follow-Up assessment (T2). The total duration of study participation for each subject will be approximately 19 weeks, including evaluation at T0, treatment and evaluation at T1 and T2. Individuals in the experimental group (VRT) will undergo a virtual reality-based sensorimotor rehabilitation. Control group (CT) subjects will undergo the same rehabilitation of VR subjects, in terms of intensity, time and type, but with the virtual reality turned off.

CONDITIONS

Official Title

Virtual Reality Rehabilitation in Neck Pain Subjects

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult individuals aged 18 to 70 years
  • Diagnosis of Neck Pain including Chronic Neck Pain or Whiplash
  • Normal or corrected vision
Not Eligible

You will not qualify if you...

  • Declined to provide informed consent
  • Presence of systemic infection or metabolic, neurological, or muscular degenerative disorders
  • History of cervical spinal pathology, fracture, or surgery
  • Radiculopathy
  • Vestibular impairments
  • Epilepsy
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

IRCSS Ospedale San Raffaele

Milan, MI, Italy, 20132

Actively Recruiting

Loading map...

Research Team

S

Sandro Iannaccone, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here