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Effect of Transitional Care Model-Based Interventions for Patients with Stroke and Their Caregivers on Increasing Caregiver Competence and Patient Outcomes: A Study Protocol for a Randomized Controlled Trial

AIM: This is a study protocol designed to evaluate the effect of transitional care model based interventions for patients with stroke and their caregivers on the caregivers’ perceived competency, their preparedness for caregiving, increasing their electronic health literacy, reducing burnout, the ra...

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Detalles Bibliográficos
Autores principales: Demir Avcı, Yasemin, Gözüm, Sebahat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Florence Nightingale Journal of Nursing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245027/
https://www.ncbi.nlm.nih.gov/pubmed/34263236
http://dx.doi.org/10.5152/FNJN.2021.19214
Descripción
Sumario:AIM: This is a study protocol designed to evaluate the effect of transitional care model based interventions for patients with stroke and their caregivers on the caregivers’ perceived competency, their preparedness for caregiving, increasing their electronic health literacy, reducing burnout, the rate of patients’ hospital readmissions, and the frequency of pressure injuries. METHOD: The study protocol was planned as a randomized controlled trial with parallel arms. The study will include 70 patients with stroke and their caregivers. Multiple interventions (TEMpEST-Transitional Care Model Stroke Turkey), including at least 3 face-to-face interviews at the hospital, distance education via web, and telephone communications for 3 months, and 1 home visit within 7 days of discharge will be applied to the study group. The control arm will receive routine care. RESULTS: Findings will give after then when completed the study protocol. CONCLUSION: This study will evaluate the feasibility of interventions TEMpEST and its effect on patients with stroke and their caregivers. TRIAL REGISTRATION: The trial was registered with the ClinicalTrials.gov protocol registration and results system (PRS) (ClinicalTrials.gov reference NCT03708835).