直接面向用户的数字心理健康工具的管理:强调透明度而不是家长式作风

IF 2.3 3区 哲学 Q1 ETHICS
Om D. Panda, Charles E. Binkley
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引用次数: 0

摘要

正如Amitabha Palmer和David Schwan在他们的文章《数字心理健康工具和人工智能治疗聊天机器人:一种平衡的监管方法》中所指出的那样,数字心理健康工具越来越多地在传统临床环境之外使用,创造了一种超越现有监管范围的参与模式。引入直接面向用户的概念(将个人作为自主主体进行自我调节、增强和意义创造),我们建议从Palmer和Schwan批评的家长式作风和严格的标准转向以人为中心的治理方法,在这种方法中,激进的透明度、个人代理和共享责任本身就是标准。透明度通过可理解地披露数据、有效性和激励机制,使用户能够根据个人目标和价值观评估权衡,从而实现知情选择。不断发展的问责制框架,如具有集体责任的自愿认证,加强了这一模式的可扩展性和道德规范,这也可以广泛应用于其他数字卫生工具和认知增强技术。这种治理框架促进了个性化的、参与性的生态系统,使新一代工具更容易获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Governance of Direct-to-User Digital Mental Health Tools: Emphasizing Transparency over Paternalism

Digital mental health tools are increasingly used outside traditional clinical settings, creating an engagement paradigm beyond the existing regulatory scope, as noted by Amitabha Palmer and David Schwan in their article “Digital Mental Health Tools and AI Therapy Chatbots: A Balanced Approach to Regulation.” Introducing the direct-to-user concept (which concerns individuals as autonomous agents navigating self-regulation, enhancement, and meaning making), we propose a shift from paternalism and rigid standards critiqued by Palmer and Schwan toward a human-centered governance approach in which radical transparency, individual agency, and shared accountability are themselves the standards. Transparency enables informed choice through intelligible disclosure of data, validity, and incentives, which empower users to assess trade-offs based on personal goals and values. Evolving accountability frameworks, such as voluntary certification with collective liability, reinforce the scalability and ethics of this model, which can also be broadly applied to other digital health tools and cognitive-enhancement technologies. This governance framework fosters individualized, participatory ecosystems to make this new generation of tools more accessible.

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来源期刊
Hastings Center Report
Hastings Center Report 医学-卫生保健
CiteScore
3.50
自引率
3.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: The Hastings Center Report explores ethical, legal, and social issues in medicine, health care, public health, and the life sciences. Six issues per year offer articles, essays, case studies of bioethical problems, columns on law and policy, caregivers’ stories, peer-reviewed scholarly articles, and book reviews. Authors come from an assortment of professions and academic disciplines and express a range of perspectives and political opinions. The Report’s readership includes physicians, nurses, scholars, administrators, social workers, health lawyers, and others.
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