Objective: To determine the relationship between symptoms of schizophrenia and caregiver burden/distress among caregivers of people with schizophrenia in southwestern Nigeria.

Method: One hundred and one family caregivers of 101 patients with schizophrenia were recruited into the study. Caregivers were screened with the Zarit Burden Interview (ZBI) to measure caregiver burden and the 30 item General Health Questionnaire (GHQ-30) to measure psychological distress. Patients were interviewed using the Brief Psychiatric Rating Scale (BPRS) and the Scale for the Assessment of Negative Symptoms (SANS) to rate psychopathology.

Results: More than half of the caregivers were females (58.4%). About one third of caregivers (33.7%) were experiencing moderate/severe levels of burden even though the mean burden score of 32.6± 14.1 for the sample was in the mild/moderate range on the ZBI scale. Using regression analysis, it was found that higher caregiver burden scores were associated with negative symptoms of asociality-anhedonia, whereas high GHQ-30 scores were associated with inattention and avolition. High caregiver burden scores were also associated the patient being unemployed and the caregiver having lower education, whereas high levels of emotional distress in the caregiver was related to the patient being female and the patient having a lower education level.

Conclusions: These results underscore the need for continued intervention for family members of Schizophrenic patients. Part of the care plan for the caregiver should include education on the negative symptoms of the illness.

Download full-text PDF

Source

Publication Analysis

Top Keywords

caregiver burden
12
negative symptoms
12
scores associated
12
psychological distress
8
family caregivers
8
schizophrenic patients
8
burden scores
8
lower education
8
caregiver
7
caregivers
6

Similar Publications

Caregivers of children with asthma can become overwhelmed by the burden of care provision. Guided by the socioecological framework, we examined individual and system-level factors associated with caregiver health-related quality of life (HRQoL) among preschool children (aged two to six years) enrolled in a multilevel home- and school-based asthma educational intervention in Baltimore, Maryland. Primary outcome was caregiver HRQoL measured at baseline and six months.

View Article and Find Full Text PDF

Background And Objectives: The study seeks to elucidate the pathways by which the Caregiver TLC psycho-educational program impacts the psychological health of caregivers by examining the degree to which changes in self-efficacy, personal gains, and emotional support mediate the changes on perceived depression, anxiety and burden.

Research Design And Methods: Using pre-post data from the Caregiver TLC randomized controlled trial (n = 81) for each outcome and mediator pair, a series of multiple regression models were executed to test the degree to which the program's total effects on changes in depression, burden and anxiety from baseline to post-intervention are due to changes in each mediator variable from pre- and post-intervention assessments. Caregivers were primarily female (85%), White (62 %), Black (38%), with a median age of 62 and household income of $75,000+.

View Article and Find Full Text PDF

Exploring the perspectives of early-stage postoperative glioblastoma patients and their caregivers on end-of-life care planning: An exploratory qualitative interview study.

Appl Nurs Res

February 2025

Institute of Community Health Care, College of Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King's College London, UK. Electronic address:

Aim: Compare the convergent and divergent viewpoints of early-stage postoperative patients with glioblastoma and their caregivers on end-of-life care planning in Taiwan.

Background: Decision-making capacity in patients with glioblastoma may be compromised as disease progresses, making early future care planning essential to ensure that the provided care aligns with patients' goals. However, within many Asian cultures, the tendency to avoid discussions about death can lead patients to feel hesitant about addressing end-of-life care options.

View Article and Find Full Text PDF

Context: Persons with advanced multiple sclerosis (MS) require care beyond the disease modifying treatments offered in conventional MS clinics to address their complex physical and psychosocial needs. In the novel MS Comprehensive and Palliative Care (MSCPC) Program, an MS neurologist, palliative care specialist, and physiatrist collaborate to identify these needs and improve symptom control.

Objectives: To characterize the medical, physical, and psychosocial concerns of persons with advanced disability from MS and describe the recommended interventions of the MSCPC Program.

View Article and Find Full Text PDF

: Depression is a common geriatric problem globally. It is particularly burdensome in low- and middle-income countries, where care for older people mainly relies on the family in the absence of long-term care facilities. This study aimed to assess the level of caregivers' burden among family caregivers who are taking care of older persons with depression in the home care setting within the communities of Chiang Mai, Northern Thailand.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!