Ireland
--:--IST
Recruiting Not applicable

Using Immersive Virtual Reality for the Upper Limb Rehabilitation of Post-stroke Subjects

NCT06892886 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2023-03-01
Last updated
2025-03-25

Condition(s) studied

Sub-acute Stroke

Investigational drug(s) / intervention(s)

Virtual Reality

Virtual Reality: Four tasks, uni and bi-manuals, will be proposed for the treatment of the patient's paretic upper limb in virtual-apartment for improving the relevance and the transferability of the movements requested.

Study summary

Stroke produces brain damages that results in sensory, motor, and cognitive impairments which reduce the patient's quality of life and social participation. Upper limb recovery is a complex process whose goal is to allow the patients to gain, in part or completely, independence in daily living activities, for that it represents one of the most important rehabilitation focus. Virtual reality is a fairly recent approach able to simulate concrete movements and functional tasks in a higher dosage compared to other therapies. It seems that the use of VR could improve limb function, however, the amount of this gain is still unclear because of insufficient evidence. This study aims at quantitatively investigating the effectiveness of an HMD immersive virtual reality system on the upper limb functioning in subacute stroke survivors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * diagnosis of first, ischemic or hemorrhagic, stroke verified by brain imaging within 4 week * upper limb motor impairment defined by an upper extremity score \<55 on the Fugl-Meyer Assessment Exclusion Criteria: * neurological conditions in addition to stroke that may affect motor function * other medical conditions likely to interfere with the ability to safely complete the study protocol * impaired cognitive functioning that influences the ability to give informed consent * severe neuropsychological disorders * visual impairment * severe upper-limb pain defined as \> 7 on the Visual Analogue Scale

Primary outcome measure(s)

  • Changes in upper limb impairment — Score changes before (T0) and after (T1) the 4 weeks of treatment and at 6-month follow-up (T2)
    Motor recovery will be assessed through the Fugl Meyer Assessment - Upper Extremity

Trial sites (1)

FacilityCityRegionStatus
Ferrara University Hospital Ferrara Italy Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06892886 on ClinicalTrials.gov ↗ ← All trials in Italy