Determinant Factors of Stress in Caregivers of Patients With Schizophrenia: Cross-Sectional Study.

IF 2 Q3 HEALTH CARE SCIENCES & SERVICES
Isymiarni Syarif, Hasnawati Amqam, Saidah Syamsuddin, Veni Hadju, Syamsiar Russeng, Yusran Amir
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引用次数: 0

Abstract

Background: Caregivers of individuals with schizophrenia face ongoing psychological and emotional burdens due to the chronic and relapsing nature of the disorder and the complexity of caregiving. Prolonged exposure to caregiving stress characterized by emotional exhaustion, role overload, and lack of social support has been consistently associated with poor mental health outcomes among caregivers, including depression and anxiety.

Objective: This study aimed to assess stress levels among caregivers of patients with schizophrenia and identify the key determinants of caregiver stress.

Methods: This study used a cross-sectional survey that was conducted between June and August 2024 at the Labakkang District Health Center, South Sulawesi, Indonesia. A total of 110 female caregivers participated in the study. Data were collected using validated questionnaires to measure stress levels and related factors. Statistical analyses included chi-square tests to identify associations and partial least squares structural equation modeling to examine the strength and direction of relationships between variables.

Results: This study included 110 female caregivers of individuals with schizophrenia. The majority were early older people (48/110, 44%), had a basic level of education (elementary to junior high school; 45/110, 46%), were unemployed (83/110, 75%), and had been providing care for more than 10 years (42/110, 38%). A total of 58 of 110 (53%) caregivers experienced mild levels of stress, while 63 of 110 (57%) caregivers reported a moderate caregiving burden. Additionally, 64 of 110 (58%) caregivers reported challenges related to patient treatment nonadherence, and 58 of 110 (53%) caregivers experienced low levels of social stigma. Most caregivers (69/110, 63%) adopted adaptive coping strategies; however, more than half reported low levels of knowledge (59/110, 54%) and limited access to health information (73/110, 66%). The chi-square analysis identified several statistically significant associations with stress: age (P=.03), education (P<.001), caregiving burden (P<.001), knowledge (P<.001), coping strategies (P<.001), treatment nonadherence (P=.004), and perceived stigma (P=.003). Further, partial least squares structural equation modeling analysis showed that caregiving burden (r=0.672), stigma (r=0.921), and limited knowledge (r=0.909) were positively correlated with stress. In contrast, social support was strongly negatively associated with stress (r=-0.872), indicating its protective role.

Conclusions: These findings underscore the critical need for targeted interventions that enhance social support networks, reduce stigma, and strengthen caregivers' coping capacities. Strengthening these dimensions is essential to mitigating the psychological toll of caregiving and sustaining caregivers' functional well-being. Evidence increasingly supports that empowering caregivers through structured support systems and educational initiatives can substantially alleviate stress-related burdens and improve care continuity for individuals with schizophrenia.

精神分裂症患者照护者压力的决定因素:横断面研究。
背景:由于精神分裂症的慢性和复发性以及护理的复杂性,精神分裂症患者的照顾者面临着持续的心理和情感负担。长期暴露于以情绪衰竭、角色超载和缺乏社会支持为特征的护理压力下,一直与护理者的心理健康状况不佳有关,包括抑郁和焦虑。目的:本研究旨在评估精神分裂症患者照顾者的压力水平,并确定照顾者压力的关键决定因素。方法:本研究采用横断面调查,于2024年6月至8月在印度尼西亚南苏拉威西省Labakkang地区卫生中心进行。共有110名女性看护人参与了这项研究。数据收集使用有效的问卷来测量压力水平和相关因素。统计分析包括卡方检验来确定关联,偏最小二乘结构方程模型来检验变量之间关系的强度和方向。结果:本研究纳入了110名精神分裂症患者的女性照护者。大多数是早期老年人(48/110,44%),具有基本的教育水平(小学到初中;45/110(46%),失业(83/110,75%),提供护理10年以上(42/110,38%)。110名照顾者中有58名(53%)经历了轻度压力,而110名照顾者中有63名(57%)报告了中度照顾负担。此外,110名护理人员中有64名(58%)报告了与患者治疗依从性相关的挑战,110名护理人员中有58名(53%)经历了低水平的社会耻辱。大多数照护者(69/110,63%)采用适应性应对策略;然而,一半以上的人报告知识水平低(59/110,54%),获得卫生信息的机会有限(73/110,66%)。卡方分析发现,年龄(P= 0.03)、教育程度(P= 0.03)与压力有统计学意义的关联。结论:这些发现强调了有针对性的干预措施的必要性,这些干预措施可以增强社会支持网络,减少耻耻感,增强照顾者的应对能力。加强这些方面对于减轻照护的心理代价和维持照护者的功能健康至关重要。越来越多的证据支持,通过结构化的支持系统和教育举措赋予护理人员权力,可以大大减轻与压力相关的负担,并改善对精神分裂症患者的护理连续性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JMIR Formative Research
JMIR Formative Research Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
9.10%
发文量
579
审稿时长
12 weeks
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