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NCT06366360Recruiting

Immersive Virtual Reality Treatment for Unilateral Spatial Neglect

Rehabilitation of Unilateral Spatial Neglect Using an Immersive Virtual Reality Music Practice Program

Source: ClinicalTrials.gov · Last updated 17 Sept 2026

Brief summary (registry, in English)

Unilateral Spatial Neglect (USN) is a relatively common neuropsychological syndrome following stroke. It is characterized by difficulties in detecting, orienting and identifying events located in the hemispace contralateral to a brain lesion, unrelated to a primary motor or sensory disorder. Numerous methods have been developed for the rehabilitation of this syndrome. However, limitations in terms of efficacy are highlighted. These limitations may be linked to the fact that these methods are restricted to certain sensory modalities, thus failing to take into account the heterogeneity of the syndrome. Moreover, some patients' adherence to rehabilitation programs can also be complicated by motivational difficulties. Immersive Virtual Reality could help overcome these limitations. Indeed, it enables the introduction of new sensory modalities, notably auditory, to support a better apprehension of space. The main objective of this study is to determine the efficacy of an immersive virtual reality rehabilitation protocol based on musical practice in patients suffering from USN. This study also aims to explore the benefits of this rehabilitation protocol on patients' daily lives, as well as to explore the influence of patients' mood and motivation on the benefits of the immersive virtual reality rehabilitation protocol. To achieve these goals, patients will benefit from immersive virtual reality rehabilitation based on music practice. This rehabilitation will be compared to conventional USN rehabilitation. To this end, patients will be divided into two groups: classical rehabilitation only or classical rehabilitation and immersive virtual reality in parallel. Each patient will be randomly assigned to one of the two groups for a period of 2 weeks. Pre- and post-rehabilitation assessments will be provided.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
27 Mar 2024
Start date
11 Mar 2024
Primary completion date
12 Jun 2024
Lead sponsor
Hopitaux de Saint-Maurice
Diseases
Stroke
NCT number
NCT06366360

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 11 Mar 2024 to the primary completion date, 12 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Epilepsy or migraine
  • Major hearing impairment
  • Pre-existing cognitive impairment (MMSE \< 20)
  • Major disorders of verbal comprehension preventing the protocol

Other

  • Major vision problems
  • Refusal to sign consent form

Who the study is looking for

  • Men and women over 18 years
  • Free and informed written consent
  • Enrolled in the French social security system
  • Cerebral lesion of vascular origin
  • Unilateral spatial neglect syndrome

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hôpitaux de Saint-Maurice
Coordinator of this site? Confirm its status
Saint-MauriceFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.