Skip to content

VIRTUAL REALITY IN CERVICAL RADICULOPATHY PATIENTS

EFFECT OF IMMERSIVE VIRTUAL REALITY ON PAIN, PROPIOCEPTION AND BALANCE IN CERVICAL RADICULOPATHY PATIENTS

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07195981
Enrollment
42
Registered
2025-09-29
Start date
2025-10-01
Completion date
2026-02-28
Last updated
2026-03-25

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

Conditions

Radiculopathy

Brief summary

PURPOSE: to investigate the effect of immersive virtual reality on pain, proprioception, and balance in cervical radiculopathy patients BACKGROUND: Cervical radiculopathy (CSR) is a disabling condition that significantly impairs a person's ability to function physically, The application of virtual reality (VR) in rehabilitation therapy offers new possibilities. In addition to the neck-specific sensorimotor training, which appears to improve neck mobility.

Detailed description

Fourty two participants with unilateral cervical radiculopathy. from both sexes were participated in this study. The patients were randomly divided into two equal groups; Study group (22 patients): received the selected physical therapy program in addition to virtual reality using Oculus glasses. (22 patients): received receive a selected physical therapy program only (Therapeutic Ultrasound device, Transcutaneous Electrical Nerve Stimulation (TENS) and Hot packs) (12 sessions) three times per week. The evaluation methods by VR ,CROM Device ,Neck disability scale, VAS, joint position error test .

Interventions

DEVICEvirtual reality

The virtual reality (VR) technology is defined as a system that allows users to interact with images and sounds in a virtual environment, which can stimulate responses and provide real-time feedback concerning their performance.

OTHERselected physical therapy

selected physical therapy program only included: (Therapeutic Ultrasound device, Transcutaneous Electrical Nerve Stimulation (TENS) and Hot packs)

Sponsors

October 6 University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Fourty two participants with unilateral cervical radiculopathy. * Participants are complaining of neck pain radiating unilaterally down to one arm. * Their ages range from 35-50 years. * They are referred by a neurologist with a diagnosis of unilateral cervical radiculopathy.

Exclusion criteria

* 1\) Cervical myelopathy. 2) Patients with previous cervical surgery. 3) Inflammatory diseases such as rheumatoid arthritis or ankylosing spondylitis 4) Any other musculoskeletal disorders of the spine or upper extremity.

Design outcomes

Primary

MeasureTime frameDescription
Biodex balance systemsix weekThe Biodex balance system considered a reliable evaluation tool for balance include overall stability index
Neck Proprioceptionsix weekNeck Proprioception by cervical joint position error via Overhead Laser Pointer

Secondary

MeasureTime frameDescription
Cervical range of motion (CROM) goniometer device measurementssix weekThe CROM is an inclinometers system with a gravitational reference that is suitable for evaluating the active cervical spine movements in different direction
Neck disability indexsix weekThe NDI is a validated self-report questionnaire to detect the level at which the neck pain
Visual analogue scale for painsix weekThe VAS-p is a method for measuring the intensity of pain on a horizontal straight line of fixed length (10 cm)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026