Clinical Research Directory

Inclusion Criteria: * Both male and female patients were included in the study. * The age range of participants was between 45 and 60 years. * Participants that were diagnosed with ischemic stroke patient. * Participants had experienced sub-acute ischemic stroke, specifically 15 days to 12 weeks post-stroke. * Montreal Cognitive Assessment scores falling within the range of 18-24 were necessary. * Modified Ashworth scale scores had to be less than +1 * National Institutes of Health Stroke Scale (NIHSS) score falling within the range of 1 to 15 were necessary. * Participants feel no pain from the vibrator. * It was anticipated that participants would either be able to give informed consent or have a legal representative who could do so. Exclusion Criteria: * People who had a history of serious neurological or mental conditions that would have impeded lower limb motor recovery-aside from stroke-were not included. * Individuals with severe arthritis or joint injuries, among other illnesses that would have interfered with treatment or evaluations, were not allowed to participate. * Individuals who had significant hearing or vision impairments that would have hampered treatment or evaluations were not included. * Individuals undergoing anti-spatial therapy or other clinical trials, those with bilateral brain lesions, and those with ischemic involvement of the cerebellum or basal ganglia were not allowed to participate. * Participants having metal implants e. g cardiac pacemaker and skin lesion at the site of stimulation electrodes were excluded.