Ischemic stroke Circulatory System Stroke, not specified as haemorrhage or infarction
Conditions
Interventions
Patients qualified by the doctor to the study group before each unit of rehabilitation training had heart rate (HR) and blood pressure (RR) measurements. Improvement training has always been selected
Sponsors
Wroclaw University of Health and Sport Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Consent to participate in the trial 2. 45-65-year-old patients who suffered an ischemic stroke 3. In the regeneration and compensation period after a stroke 4. Patients admitted for early post-stroke rehabilitation
Exclusion criteria
Exclusion criteria: 1. Complete lack of movement of the upper limb 2. Very fit upper limb 3. Time from stroke longer than 30 days 4. Complete lack of cooperation on the part of the patient (global aphasia, lack of patient consent) 5. Complete stiffening of the shoulder joint
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The concentrations of BDNF, IGF-1, HGF, NT-3, NGF, VEGF, serotonin, lactate, dopamine, and cortisol from the blood serum at baseline, 14, 28, and 42 weeks (every 2 weeks during rehabilitation in the ward and after its completion, in the 6th week). Each patient will have blood drawn four times. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Everyday activities assessed using the Barthel Scale at baseline, 14, 28, and 42 weeks 2. Ability to perform complex everyday activities assessed using the Instrumental Activities of Daily Living Scale (IADL Scale) at baseline, 14, 28, and 42 weeks 3. Hand dexterity assessed using the Frenchay hand test (Frenchay Arm Test) at baseline, 14, 28, and 42 weeks 4. Degree of depression assessed using the Anxiety and Depression Scale (HADS Scale) at baseline, 14, 28, and 42 weeks | — |
Countries
Poland
Outcome results
None listed