Actively Recruiting
Robotic Rehabilitation Vs Occupational Therapy Chronic Stroke Upper Limb Rehabilitation
Led by University of Florence · Updated on 2025-03-19
72
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
U
University of Florence
Lead Sponsor
F
Fondazione Don Carlo Gnocchi Onlus
Collaborating Sponsor
AI-Summary
What this Trial Is About
The functional recovery of the upper limb represents a critical element in post-stroke rehabilitation; hemiplegic/hemiparetic patients who achieve optimal recovery are a minority, and incomplete recovery has relevant consequences both on functioning and on quality of life of those who survive a stroke. The project aims to assess the effects on the functional recovery, with manual dexterity as the primary outcome, of a treatment protocol using an innovative tool (Gloreha Sinfonia) that enables assisted execution of three-dimensional tasks combined with Serious Games for cognitive stimulation, targeting the functional recovery of the upper limb in patients with stroke outcomes at least 6 months after the acute event (chronic phase). Patients with residual dysfunction of the upper limb, at least 6 months after the stroke, will be randomly assigned to the Robotic Rehabilitation group (ROBOT), the Occupational Therapy group (OT), focused on the use of the upper limb in functional tasks (task-oriented training), or the control group (CT - prescription of a home exercise program). Patients in the ROBOT and OT groups will undergo a total treatment period of 5 weeks, with 3 sessions per week lasting 1 hour, for a total of 15 sessions/hours of treatment. Patients assigned to the CT group will undergo an initial functional assessment required for defining the exercise program. All patients will be evaluated at baseline (T0), at a 5-week interval (T1), and 6 months after the end of treatment (T2). Outcome indicators include measures of manual dexterity/upper limb performance, anxiety/depression, cognitive abilities, and patient-perceived outcomes. The analysis of Surface Plasmon Resonance imaging (SPRi) of serum exosome content, detected at T0, T1, and T2, will be correlated with variations in functional measures to verify the hypothesis that induction of neuroplasticity underlies any observed changes. Short- and medium-term effects on functional, psychological outcomes, as well as indicators of neuroinflammation and neural regeneration from serum analysis using innovative SPRi, will be compared among the 3 groups.
CONDITIONS
Official Title
Robotic Rehabilitation Vs Occupational Therapy Chronic Stroke Upper Limb Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- First ischemic or hemorrhagic stroke at least 6 months prior
- Persistent motor deficit in the affected upper limb with Motricity Index between 18 and 77
- Willingness to participate and provide informed consent
You will not qualify if you...
- Severe spastic hypertonia at wrist and fingers (Modified Ashworth Scale 3 or higher)
- Orthopedic, rheumatological, or peripheral nervous system disorders affecting the paretic upper limb
- Neurodegenerative or neuromuscular disorders
- Acute illnesses affecting other body systems
- Severe cognitive, language, or behavioral disorders limiting understanding or participation
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fondazione Don Carlo Gnocchi Onlus
Florence, Italy, Italy, 50100
Actively Recruiting
Research Team
F
Francesca Cecchi, MD
CONTACT
C
Chiara Castagnoli, PT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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