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Assessing Informed Consent in an Opioid Relapse Prevention Study with Adults under Current or Recent Criminal Justice Supervision

机译:在当前或最近的刑事司法监督下对成年人的阿片类药物复发预防研究进行知情同意评估

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摘要

Concerns persist that individuals with substance use disorders who are under community criminal justice supervision experience circumstances that might compromise their provision of valid, informed consent for research participation. These concerns include the possibilities that desire to obtain access to treatment might lead individuals to ignore important information about research participation, including information about risks, or that cognitive impairment associated with substance use might interfere with attending to important information. We report results from a consent quiz (CQ) administered in a multisite randomized clinical trial of long-acting naltrexone to prevent relapse to opioid use disorder among adults under community criminal justice supervision—a treatment option difficult to access by this population of individuals. Participants were required to answer all 11 items correctly before randomization. On average, participants answered 9.8 items correctly (89%) at baseline first attempt (n=306). At week 21 (n=212), participants scored 87% (9.5 items correct) without review. Performance was equivalent to, or better than, published results from other populations on a basic consent quiz instrument across multiple content domains. The consent quiz is an efficient method to screen for adequate knowledge of consent information as part of the informed consent process. Clinical researchers who are concerned about these issues should consider using a consent quiz with corrected feedback to enhance the informed consent process. Overall, while primarily useful as an educational tool, employing a CQ as part of the gateway to participation in research may be particularly important as the field continues to advance and tests novel experimental treatments with significant risks and uncertain potential for benefit.
机译:人们仍然担心,在社区刑事司法监督下的物质滥用障碍患者所经历的情况可能会损害他们为研究参与提供有效的知情同意的能力。这些担忧包括可能获得治疗的愿望,可能导致个人忽略有关研究参与的重要信息,包括有关风险的信息,或者与药物使用相关的认知障碍可能会干扰获得重要信息的可能性。我们报告了一项在长效纳曲酮的多站点随机临床试验中进行的同意测验(CQ)的结果,该试验可防止在社区刑事司法监督下的成年人中复发至阿片类药物使用障碍-这是该人群难以获得的治疗选择。随机分组之前,要求参与者正确回答所有11个项目。平均而言,参与者在基线首次尝试时(n = 306)正确回答了9.8个项目(占89%)。在第21周(n = 212),参与者得分为87%(正确的9.5项),没有进行任何评论。在跨多个内容领域的基本同意测验工具上,其效果与其他人群的结果相当或更好。同意测验是一种筛选有效信息的有效方法,它是知情同意过程的一部分。关注这些问题的临床研究人员应考虑使用具有正确反馈的同意测验,以增强知情同意程序。总体而言,尽管CQ作为一种教育工具非常有用,但随着领域的不断发展和测试具有重大风险和不确定性的新实验方法,采用CQ作为参与研究的门户可能尤其重要。

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