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一项关于改善精神分裂症患者获得结直肠癌筛查机会的医疗机构层面实施策略的可行性研究:ACCESS2(N-EQUITY 2104)试验。

A feasibility study of provider-level implementation strategies to improve access to colorectal cancer screening for patients with schizophrenia: ACCESS2 (N-EQUITY 2104) trial.

作者信息

Fujiwara Masaki, Yamada Yuto, Etoh Tsuyoshi, Shimazu Taichi, Kodama Masafumi, Yamada Norihito, Asada Takahiro, Horii Shigeo, Kobayashi Takafumi, Hayashi Teruo, Ehara Yoshitaka, Fukuda Kenji, Harada Keita, Fujimori Maiko, Odawara Miyuki, Takahashi Hirokazu, Hinotsu Shiro, Nakaya Naoki, Uchitomi Yosuke, Inagaki Masatoshi

机构信息

Department of Neuropsychiatry, Okayama University Hospital, Okayama, Japan.

Department of Nursing, Shimane University Hospital, Izumo, Japan.

出版信息

Implement Sci Commun. 2024 Jan 4;5(1):2. doi: 10.1186/s43058-023-00541-0.

Abstract

BACKGROUND

People with schizophrenia have a lower colorectal screening rate than the general population. A previous study reported an intervention using case management to encourage colorectal cancer screening for patients with schizophrenia in psychiatric outpatient settings. In this feasibility study, we developed provider-level implementation strategies and evaluated the feasibility of conducting a definitive trial in terms of the penetration of the intervention assessed at the patient level. Additionally, we examined the fidelity of strategies to implement the intervention at the provider level in a routine clinical psychiatric setting.

METHODS

This was a multicenter, single-arm feasibility study with medical staff at psychiatric hospitals in Japan. The provider-level implementation strategies developed in this study included three key elements (organizing an implementation team appointed by the facility director, interactive assistance using a clear guide that outlines who in the hospital should do what, and developing accessible educational materials) to overcome major barriers to implementation of the intervention and four additional elements (progress monitoring, joint meetings and information sharing among participating sites, adaptation of encouragement methods to specific contexts, and education of on-site staff), with reference to the elements identified in the Expert Recommendations for Implementing Change (ERIC). The feasibility of the strategies was evaluated by the proportion of patients who were eligible for encouragement (patients with schizophrenia aged 40, 50, or 60) who received encouragement. We set the goal of providing encouragement to at least 40% of eligible patients at each site.

RESULTS

Two public and four private psychiatric hospitals in Okayama and Shimane prefectures participated in this study. Regarding fidelity, all elements of the strategies were conducted as planned. Following the procedures in the guide, each team prepared and provided encouragement according to their own facility and region. Penetration, defined as the proportion of eligible patients who received encouragement, ranged from 33.3 to 100%; five of the six facilities achieved the target proportion.

CONCLUSIONS

The provider-level implementation strategies to implement encouragement were feasible in terms of penetration of the intervention assessed at the patient level. The results support the feasibility of proceeding with a future definitive trial of these strategies.

TRIAL REGISTRATION

jRCT, jRCT1060220026 . Registered on 06/04/2022.

摘要

背景

精神分裂症患者的结直肠癌筛查率低于普通人群。此前一项研究报告了一项干预措施,即在精神科门诊环境中采用病例管理来鼓励精神分裂症患者进行结直肠癌筛查。在这项可行性研究中,我们制定了医疗机构层面的实施策略,并从患者层面评估干预措施的渗透率方面,评估了开展一项确定性试验的可行性。此外,我们还研究了在常规临床精神科环境中,在医疗机构层面实施干预措施的策略的保真度。

方法

这是一项在日本精神病医院与医务人员开展的多中心单臂可行性研究。本研究制定的医疗机构层面的实施策略包括三个关键要素(组建由机构负责人任命的实施团队、使用明确指南进行互动协助,该指南概述医院内谁应该做什么,以及开发易于获取的教育材料)以克服干预措施实施的主要障碍,以及另外四个要素(进展监测、参与站点之间的联席会议和信息共享、根据具体情况调整鼓励方法,以及对现场工作人员进行培训),参考了《实施变革专家建议》(ERIC)中确定的要素。通过接受鼓励的符合鼓励条件的患者(40岁、50岁或60岁的精神分裂症患者)比例来评估策略的可行性。我们设定的目标是在每个站点至少为40%的符合条件的患者提供鼓励。

结果

冈山和岛根县的两家公立医院和四家私立精神病医院参与了本研究。关于保真度,策略的所有要素均按计划实施。各团队按照指南中的程序,根据自身机构和地区情况准备并提供鼓励。以接受鼓励的符合条件患者的比例定义的渗透率在33.3%至100%之间;六个机构中有五个达到了目标比例。

结论

就患者层面评估的干预措施渗透率而言,实施鼓励的医疗机构层面实施策略是可行的。结果支持对这些策略进行未来确定性试验的可行性。

试验注册

jRCT,jRCT1060220026。于2022年4月6日注册。

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