Stroke. Cerebellar stroke syndrome
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: This group will be supported by the researcher in accordance with the transitional care program from the second day of hospitalization (after ne
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The diagnosis of stroke was confirmed by a neurologist who was selected to be a resident of the study group in Isfahan. Willingness to participate in the study. Be hospitalized for the first time with a stroke diagnosis. Phone number to call. Patients with at least GCS 13-15. Patients selected for the study group reside in Isfahan.
Exclusion criteria
Exclusion criteria: The patient should not have a decreased consciousness. Has no other neurological or mental illness. Has been hospitalized for the first time with a stroke diagnosis The patient has not undergone skull or brain surgery. Patients with perceptual or global aphasia are not included in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome measure of quality of life in stroke patients. Timepoint: Before the intervention (pre-test), after the intervention in the tenth week after discharge (post-test). Method of measurement: Specific standard questionnaire for quality of life after stroke (SS-QOL).;The ability to perform daily living activities in stroke patients. Timepoint: Before the intervention (pretest), after the intervention in the tenth week after discharge (post-test). Method of measurement: Barthel questionnaire will be used. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahla Abolhassani
Esfahan University of Medical Sciences
Outcome results
None listed