Stroke Clinical Trial
Official title:
Feasibility and Efficacy of a Robotic Device for Hand Rehabilitation in Hemiplegic Stroke Patients: a Randomized Pilot Controlled Study
Hand recovery following cerebral stroke is complex and requires intensive training. The investigators aimed to evaluate the feasibility and efficacy of robot-assisted hand rehabilitation compared to physiotherapist-guided treatment in recovering dexterity and hand strength in hospitalized sub-acute hemiplegic patients. Design. 30 patients affected by stroke from cerebral ischemia or hemorrhage (Ashworth spasticity index <3) were randomized. Patients in the Treatment group received intensive hand training with Gloreha, a hand rehabilitation glove that provides computer-controlled, repetitive, passive mobilization of the fingers, with multisensory feedback. Patients in the Control group received conventional intensive hand rehabilitation under physiotherapist guidance. Hand motor function (Motricity Index, MI), fine manual dexterity (Nine Hole Peg Test, NHPT) and strength (Grip and Pinch test) were measured at baseline and after rehabilitation, and the differences between final and basal results were compared between groups.
Upper limb recovery, particularly that of the hand, is complex in patients with cerebral
stroke and requires an intensive approach.
Regarding upper limb rehabilitation, several research groups have developed robotic devices
to provide passive and/or active movements. Their use appears to reduce the motor deficit of
the arm and affected hand and to improve hand function both at the wrist and fingers. Hence,
the evidence supporting specific robot-assisted rehabilitation of the hand is very promising
even if further study is required.In particular, evidence is limited about the benefit of
passive exercises and mobilization of the hemiplegic upper limb following stroke, and
further research is called for.
In this study the investigators used Gloreha, a new hand rehabilitation glove that provides
computer-controlled, repetitive and passive mobilization of the fingers, with multi-sensory
feedback. The purpose of the study was to evaluate in the rehabilitation of patients with
ischemic or hemorrhagic stroke in the sub-acute phase: 1) the feasibility of this new
neuromotor rehabilitation device 2) its efficacy in improving arm function abilities, and 3)
the costs involved.
Post-stroke patients admitted for inpatient rehabilitation between May 2013 and January 2014
were screened for enrollment. Eligible patients were randomly assigned, following a simple
randomization procedure (computerized random numbers) conducted independently of the study
investigators, to Treatment group or Control group, on a 1:1 ratio.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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