Research-active clinical services have lower mortality rates and produce higher quality care outcomes, however, recruiting participants to clinical research in the National Health System (NHS) remains challenging.1 A recent study, assessing the feasibility of clinical staff electronically documenting patient consent to discuss research participation, indicated very low patient uptake, limiting its effectiveness as a strategy for improving access to research.2 A follow-on study comparing this ‘opt-in’ approach with an ‘opt-out’ approach, whereby patients are informed about research opportunities unless they indicate otherwise, found that patients and staff favoured an ‘opt-out’ approach and wanted research to be more accessible.3 Subsequently, in August 2021, Count me In was developed and launched within Oxford Health …

中文翻译：

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确保所有有心理健康问题的患者都能在 NHS 中获得研究机会，从而促进包容性

研究活跃的临床服务具有较低的死亡率并产生更高质量的护理结果，但是，招募参与者参与国家卫生系统 (NHS) 的临床研究仍然具有挑战性。1 最近的一项研究评估了临床工作人员以电子方式记录患者同意的可行性讨论研究参与，表明患者的参与率非常低，限制了其作为改善研究机会的策略的有效性。2 一项后续研究将这种“选择加入”方法与“选择退出”方法进行了比较，通过“选择退出”方法，患者被告知除非另有说明，否则研究机会发现患者和工作人员倾向于“选择退出”方法，并希望研究更容易获得。3 随后，2021 年 8 月，牛津健康中心开发并推出了 Count me In……