The effect of vitamin D Supplementation on the fUnctional efficiency of Patients after ischemic strOke undergoing neurological Rehabilitation - a prospective, randomized Trial with a control group (D-SUPORT)
Patients who had their first ischemic stroke were admitted to the ward for early post-stroke rehabilitation
Participants in the study will be randomized (using the randomization program from the website random.org) and assigned to one of two comparison groups: group A - a group in which vitamin D supplementation at a dose of 2000 IU every morning (at 7.30 a.m.) for 6 weeks and group B (control) - group without vitamin D supplementation.
1. First ischemic stroke (time of occurrence 2 weeks before admission to the Department of Neurological Rehabilitation) 2. Stroke confirmed by MR or CT scan 3. Age >18 years old 4. No contraindications to participate in the experiment (consent of the attending physician) 5. No concomitant neurological diseases 6. Written informed consent of the patient to participate in the research
1. Patients with infection in the last 2 weeks 2. Patients who have taken vitamin D and its derivatives or calcium in the last 3 months 3. Patients with liver and kidney disorders 4. Patients with thyroid dysfunction 5. Patients with aphasia 6. Patients who do not consent to the research