The objective of this clinical trial is to measure the effect of Rehabilitation with Virtual Reality or Modified Constraint-Induced Movement Therapy on hemiparesis in patients with Cerebral Vascular Event.
The question to be answered is: What is the effect of different therapeutic modalities supported by Virtual Reality or Modified Constraint-Induced Movement Therapy compared with usual Physical and Occupational Therapy on motor recovery of paretic limbs in patients with Cerebrovascular Event?
The patients will carry out activities of:
* Virtual reality or * Movement Restriction-Induction Therapy.
The investigators will compare the changes in the functionality of the paretic hemibody with a group undergoing regular physical and occupational therapy, as well as language and treatment-related satisfaction.
Adult patients between 35 and 70 years of age and with a clinically and tomographically proven diagnosis of a cerebral vascular event in the territory of the middle cerebral artery.
Patients with hemiparesis secondary to the cerebrovascular event
Patients with a maximum Ashworth of 2 and Brunnstrom of minimum 4
Patients with or without aphasia
Patients who develop dementia or neurological-psychomotor complications during the study.
Patients who present a new cerebrovascular event during the investigation
Patients who do not complete at least 90% of the program
Patients in whom a lack of family support or secondary gain is detected.