Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The aim of the study is to investigate the effectiveness of motor and cognitive virtual environment rehabilitation on upper limb function in sub-acute patients after an acquired brain injury.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Virtual Reality rehabilitation group | Experimental | The Virtual Reality group will perform upper extremity motor rehabilitation and neurocognitive rehabilitation based on virtual reality training. |
|
| Control group | Active Comparator | The Control group will perform the same motor and neurocognitive rehabilitation but with the virtual reality turned off. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Virtual Reality rehabilitation group | Other | Three hours rehabilitation sessions every day that will consist in two hours of physiotherapy and one hour of neurocognitive rehabilitation, for 15 consecutive working days (3 weeks). 1 hour: conventional physiotherapy 1 hour: virtual reality upper extremity motor rehabilitation 1 hour: virtual reality neurocognitive training |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Fugl-Meyer Upper Extremity (FMUE) | Items are scored on a 3-point ordinal scale 0 = cannot perform; 1 = performs partially; 2 = performs fully. Maximum Score = 66 points | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Action Research Arm Test (ARAT) | From Baseline (T0) to 3 weeks of rehabilitation (T1) | |
| Change in Functional Independence Measures (FIM) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Resting state functional MRI (fMRI) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sandro Iannaccone | Contact | 0226435734 | 0039 | iannaccone.sandro@hsr.it |
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| IRCSS Ospedale San Raffaele | Milan | MI | 20132 | Italy |
Not provided
| ID | Term |
|---|---|
| D001930 | Brain Injuries |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Control group rehabilitation | Other | Three hours rehabilitation sessions every day that will consist in two hours of physiotherapy and one hour of neurocognitive rehabilitation, for 15 consecutive working days (3 weeks). 1 hour: conventional physiotherapy 1 hour: upper extremity motor rehabilitation 1 hour: neurocognitive training |
|
| Change in Mini Mental State Examination (MMSE) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| Change in Montreal Cognitive Assessment (MoCA) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| Change in Beck Depression Inventory (BDI) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| Change in 36-Item Short Form Survey (SF-36) | From Baseline (T0) to 3 weeks of rehabilitation (T1) |
| D020196 | Trauma, Nervous System |
| D014947 | Wounds and Injuries |