Objective: After acute care, the burden of caring for patients with traumatic brain injury (TBI) is mainly shouldered by the family caregivers (FCs). We aimed to explore the quality of life (QoL) of Omani FCs for patients with TBI. Methods: A total of 36 FCs and patients with TBI were recruited from one hospital. Data was collected at discharge time and eight weeks post-discharge in the period from April 2019 to December 2021. The SF-12 general health survey and preparedness for caregiving scale were used to measure the caregivers’ QoL and preparedness, respectively. The disability rating scale and the TBI symptom scale were used to measure the patient’s disability and symptoms, respectively. Paired t-test and multiple linear regression analysis were performed. Results: Most caregivers were the parent (41.7%) or child (27.8%) of the patient with TBI. Overall the caregivers had good physical QoL (PQoL) and mental health QoL (MHQoL) but low caregiving preparedness at the time of discharge. At eight weeks post-discharge, there were significant improvements in caregiving preparedness (p< 0.01), patient disability (p< 0.05), and depreciation in caregivers’ MHQoL (p< 0.05), but no change in the PQoL. The modifiable predictors of PQoL were the caregiver’s employment status and the severity of the patient’s sleep and mood problems. The predictors of MHQoL were caregiving preparedness, the patient’s inability to live independently, and the severity of mood and behavioral problems. Conclusion: Omani FCs for patients with TBI experience a negative impact on QoL, and this is correlated with the physical, emotional, and mental health symptoms of the patient.
Keywords: Caregiving, Family, Quality of Life, Caregiving Burden, Traumatic Brain Injury, Caregivers’ preparedness, Oman.