Schmaling Karen B, Kaplan Robert M
Department of Psychology, Washington State University, USA.
Clinical Excellence Research Center, Stanford University School of Medicine, USA.
J Psychiatr Res. 2023 May;161:461-466. doi: 10.1016/j.jpsychires.2023.04.004. Epub 2023 Apr 10.
Published clinical trials represent a subsample of the objective information needed to appraise treatments for depression. We characterize the extent of selective and delayed reporting in a systematic review (PROSPERO #CRD42020173606) of depression trial results registered on ClinicalTrials.gov. Inclusion criteria were studies registered on ClinicalTrials.gov with depression as the condition, had enrolled ages 18 and over, were completed between January 1, 2008 and May 1, 2019, and had posted results by February 1, 2022. Cox regression analyses of time to result posting from registration and from study completion included enrollment as a covariate. Among 442 protocols, median result posting occurred over two years after study completion and five years after registration. Among protocols with incomplete results, effect sizes (d or W) were calculated for 134 protocols. Median effect sizes for protocols with incomplete results were small (0.16, 95% CI 0.08, 0.21). For 28% of protocols, observed effects were contrary to the expected direction. Between-group effect size calculations were based on post-treatment data as pre-treatment data were inconsistently provided. Although drug and device trials in the U.S. are required to register on ClinicalTrials.gov, compliance is imperfect, and submissions are not peer reviewed. For depression treatment trials, long intervals between study completion and posting of results are common. Further, investigators often fail to report the results of statistical tests. Failure to post trial results in a timely manner and omission of statistical test reporting may lead to overestimates of treatment effects in systematic literature reviews.
已发表的临床试验只是评估抑郁症治疗方法所需客观信息的一个子样本。我们在一项对ClinicalTrials.gov上注册的抑郁症试验结果进行的系统评价(PROSPERO #CRD42020173606)中,对选择性报告和延迟报告的程度进行了描述。纳入标准为在ClinicalTrials.gov上注册的研究,以抑郁症为疾病,纳入年龄在18岁及以上,于2008年1月1日至2019年5月1日期间完成,并于2022年2月1日前公布结果。对从注册到结果公布以及从研究完成到结果公布的时间进行Cox回归分析,将纳入情况作为协变量。在442项方案中,结果公布的中位数发生在研究完成后两年以上以及注册后五年。在结果不完整的方案中,对134项方案计算了效应量(d或W)。结果不完整的方案的中位数效应量较小(0.16,95%CI 0.08,0.21)。对于28%的方案,观察到的效应与预期方向相反。组间效应量计算基于治疗后数据,因为治疗前数据提供不一致。尽管美国要求药物和器械试验在ClinicalTrials.gov上注册,但合规情况并不理想,提交的材料也未经同行评审。对于抑郁症治疗试验,研究完成与结果公布之间的间隔时间通常很长。此外,研究人员常常未能报告统计检验结果。未能及时公布试验结果以及遗漏统计检验报告可能会导致在系统文献综述中高估治疗效果。