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Emerging findings in ethics of schizophrenia research.

机译:精神分裂症研究伦理方面的新发现。

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PURPOSE OF REVIEW: We review recent publications pertaining to six topics: investigators, professional integrity, and sources of potential bias; scientific designs; protocol safeguards; influences on research participation decisions and perceptions of risk; informed consent--decision-making capacity, appreciation and the therapeutic misconception, and voluntarism; and informed consent--intervention studies. RECENT FINDINGS: Little empirical work has been conducted on investigator training and potential conflicts of interest. Numerous conceptual pieces have tackled controversial issues related to study designs, with the initial focal point being the ethics of placebo-controlled studies; only a handful of reports, however, have empirically addressed these topics. Emerging findings pertinent to protocol safeguards in schizophrenia research suggest general support by individuals with schizophrenia for a variety of safeguards. Recent work on influences on participation decisions suggests that people with schizophrenia use fundamentally similar considerations as medically ill people and healthy comparison participants--a combination of personal and altruistic motives. Much of the data-based literature has focused on informed consent. We highlight studies indicating that patients living with schizophrenia show heterogeneity in consent-related abilities but may possess key strengths in the research situation, not simply greater vulnerability as suggested in the historical literature. Furthermore, consent-related abilities appear to be enhanced with educational interventions. SUMMARY: Empirical studies focusing on a variety of ethically relevant domains in schizophrenia research are needed. Future studies should incorporate quantitative and qualitative methods, integrate perspectives of stakeholders, and investigate the effects and appropriateness of current protocol safeguards.
机译:审查目的:我们审查与六个主题有关的最新出版物:调查员,职业正直和潜在偏见的来源;科学设计;协议保障措施;对研究参与决策和风险认知的影响;知情同意-决策能力,欣赏和治疗误解以及自愿性;和知情同意书-干预研究。最近的调查结果:在调查员培训和潜在的利益冲突方面,几乎没有进行任何实证研究。许多概念性文章解决了与研究设计有关的有争议的问题,最初的重点是安慰剂对照研究的伦理学。但是,只有少数报告凭经验论证了这些主题。精神分裂症研究中与方案安全措施有关的新发现表明,精神分裂症患者普遍支持多种安全措施。关于参与决策影响的最新研究表明,精神分裂症患者使用的病因与内科疾病患者和健康的比较参与者基本相似,这是个人动机和利他动机的结合。许多基于数据的文献都集中在知情同意上。我们重点研究表明,精神分裂症患者在同意相关能力方面表现出异质性,但在研究情况下可能具有关键优势,而不仅仅是历史文献中提出的更大的脆弱性。此外,通过教育干预,与同意相关的能力似乎得到了增强。摘要:需要对精神分裂症研究中的各种伦理相关领域进行重点研究。未来的研究应纳入定量和定性方法,整合利益相关者的观点,并调查当前协议保障措施的效果和适当性。

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