Eleanor Brown, George Albert Fisher, Andrew Shelton, Daniel T Chang, Erqi Pollom
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引用次数: 0
摘要
我们需要创新的策略来提高临床试验的可及性和公平性。我们对一项由研究者发起的 II 期试验进行了回顾性研究,以确定修改临床试验设计以分散研究治疗是否能提高代表性不足群体的试验可及性。研究人员比较了在当地接受化疗的参与者与不在当地接受化疗的参与者的社会人口学特征,包括地区剥夺指数以及研究地点的旅行距离、时间和费用。在当地接受化疗的参与者居住地距离研究地点明显较远(中位数为 95.90 英里 vs 25.20 英里,p = .004),前往研究地点的时间负担较重(中位数为 115.00 分钟 vs 34.00 分钟,p = .002),前往研究地点的单次旅行相关费用较高(中位数为 62.81 美元 vs 16.51 美元,p = .004)。本研究强调了减轻与参与临床试验相关的经济和时间毒性的机会,促进了临床研究的公平性。
Advancing clinical trial equity through integration of telehealth and decentralized treatment.
Innovative strategies to increase clinical trial accessibility and equity are needed. We conducted a retrospective review of a phase II investigator-initiated trial to determine whether the modification of clinical trial design to decentralize study treatment can improve trial accessibility among underrepresented groups. Sociodemographic characteristics, including area deprivation indices, as well as study site travel distance, time, and costs were compared between enrolled participants who received chemotherapy locally and participants who did not. Participants who received chemotherapy locally lived substantially farther from the study site (median = 95.90 vs 25.20 miles, P = .004), faced a greater time burden traveling to the study site (median = 115.00 vs 34.00 minutes, P = .002), and had higher travel-related costs for a single trip to the study site (median = $62.81 vs $16.51, P = .004). This study highlights opportunities for alleviating financial and time burdens associated with clinical trial participation, promoting equity in clinical research. Trial Registration: ClinicalTrials.gov identifier: NCT04380337.