Stroke. Stroke, not specified as haemorrhage or infarction
Conditions
Interventions
Intervention 1: Intervention group: Implementation of family-centered empowerment model for family caregivers in the intervention group, in 4 sessions of two hours and in 4 consecutive days during the
Lifestyle
Intervention group: Implementation of family-centered empowerment model for family caregivers in the intervention group, in 4 sessions of two hours and in 4 consecutive days during the hospitalization
Control group: there are no interventions in this group. Measures for measuring the variables of the research will be carried out as in the intervention group.
Sponsors
Faculty of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
45 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patient entry criteria: 1. Having stroke. 2. disability degree of 3, 4 or 5 in accordance with the standard Rankin scale. 3. Educability. 4. Age 45 years and up. 5. Hospital admission for at least 4 days. 6. Transfer to the home after discharge and being under the care of the family care provider. Family caregiver entry criteria: 1. Lack of previous care of another patient with chronic illness. 2. Not having academic education in the field of medical science in the caregiver or other family members of the patient. 3. Age 18 years old and up. 4. Having reading and writing skills and ability to speak Persian 5. Calling possibility. Patient exit criteria: 1. Readmission or death of the patient before the final evaluation. 2. Not participating in implementation of the education participatory step of family-centered empowerment model. 3. Receiving an educational program except the normal schedule of the hospital during the study period. Family caregiver exit criteria: 1. Changing of the family caregiver. 2. Lack of regular participation in the implementation of family-center empowerment model steps. 3. Receiving an educational program except the normal schedule of the hospital during the study period.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ability to do daily life activities. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: Barthel Index.;Burden of care. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: Novak & Guest Caregiver Burden Inventory. | — |
Secondary
| Measure | Time frame |
|---|---|
| Perceived threat. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: Researcher-made Questionnaire of Perceived Threat.;Self-efficacy. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: General Self Efficacy-10.;Self-Esteem. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: Rosenberg Self_Esteem Scale.;Health Locus of Control. Timepoint: Before intervention, immediately after intervention, 2 weeks after intervention, 2 months after intervention. Method of measurement: Multidimensional Health Locus of Control scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNarjes Deyhoul
Faculty of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences
Outcome results
None listed