patients with stroke. Stroke,not specified as hemorrhage or infarction
Conditions
Interventions
Intervention 1: The experimental group comprised 32 people, divided into two groups of 16. For each group, the theoretical and practical class was provided in eight one-hour sessions for five weeks. T
Sponsors
University of social welfare and rehabilitation sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Consent for taking part in the study Reading and writing literacy All families of stroke patients who had a stroke one week before, and had a medical record at the hospital indicating definitive diagnosis of stroke
Exclusion criteria
Exclusion criteria: Participation of families in similar studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Burden of care. Timepoint: At the beginning of the study and six weeks after the intervention. Method of measurement: Zarit Burden Interview.;Total family Apgar score. Timepoint: At the beginning of the study and six weeks after the intervention. Method of measurement: Smilkstein Family Apgar Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Heydari
University of social welfare and rehabilitation sciences
Outcome results
None listed