Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 1:16 PM
Ignite Modification Date:
2025-12-26 @ 1:16 PM
NCT ID:
NCT06927206
Eligibility Criteria:
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.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
45 Years
Maximum Age:
60 Years
Study:
NCT06927206
Study Brief:
Protocol Section:
NCT06927206