Department of Community Mental Health & Law, National Center of Neurology and Psychiatry, National Institute of mental Health, Tokyo, Japan.
Department of Nursing Sciences, Graduate School of Human Health Sciences, Tokyo Metropolitan University, Tokyo, Japan.
Neuropsychopharmacol Rep. 2021 Dec;41(4):554-561. doi: 10.1002/npr2.12211. Epub 2021 Oct 12.
Treatment goals for mental illness have expanded from hospital discharge and improved functioning to employment, living alone, and personal realization. These changes in treatment goals have also influenced mental health research. Recent studies have addressed the development of core outcome sets focusing on clinical aspects of mental illness such as depression and anxiety. However, a well-developed framework of essential outcomes for people with mental illness (service users) who live in the community is lacking. In addition, recent worldwide trends suggest more patient and public involvement and the importance of considering multiple stakeholders' views in the area of mental health research. Purpose of this study is to explore consensus on high-priority outcome domains among multiple stakeholders in community mental healthcare fields in Japan.
A three-step approach to developing an outcome list will be used. First, we developed a long list of outcomes for community mental health through a literature review, focus group interviews with key stakeholders, and online questionnaire surveys of service users and caregivers. Second, the long list was checked and revised in a pilot study. Third, the long list will be shortened to the outcome list through the Delphi methodology with participation from multiple stakeholders.
Identifying important common outcome domains through collaboration with multiple stakeholders appears to contribute to the development of evidence for community mental health research in Japan. In addition, the study process itself may help promote patient and public involvement in education, practice, and research in the field of community mental health.
精神疾病的治疗目标已经从出院和改善功能扩展到就业、独居和个人实现。这些治疗目标的变化也影响了精神健康研究。最近的研究集中在精神疾病的临床方面,如抑郁和焦虑,制定了核心结局集。然而,对于居住在社区的精神疾病患者(服务使用者)缺乏一个完善的基本结果框架。此外,最近全球的趋势表明需要更多的患者和公众参与,并且在精神健康研究领域需要考虑多个利益相关者的观点。本研究的目的是探索日本社区精神卫生保健领域的多个利益相关者对高优先级结果领域的共识。
将采用三步法制定一个结果清单。首先,我们通过文献回顾、与主要利益相关者的焦点小组访谈以及对服务使用者和照顾者的在线问卷调查,制定了一份社区精神卫生的长清单。其次,在试点研究中检查和修订长清单。最后,通过德尔菲法,让多个利益相关者参与,将长清单缩短为结果清单。
通过与多个利益相关者合作确定重要的共同结果领域,似乎有助于为日本的社区精神健康研究提供证据。此外,研究过程本身可能有助于促进社区精神卫生领域的患者和公众参与教育、实践和研究。