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Results of a Community Randomized Study of a Faith-Based Education Program to Improve Clinical Trial Participation among African Americans

机译:一项基于信仰的教育计划以提高非裔美国人临床试验参与度的社区随机研究的结果

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This is a report of a cluster randomized clinical trial evaluating the effectiveness of a church-based educational intervention aimed at improving African Americans’ (AA) participation in clinical trials. Two hundred and twenty-one AA subjects ages ≥50 years from six predominantly AA churches were randomized to intervention or control condition. The intervention included three educational sessions about clinical trials and health disparities; control participants completed questionnaires. Primary endpoints of the study were differences in individual subjects' intentions to obtain clinical trial information and intention to join a clinical trial, as determined by 10 point scale items at baseline, three and six months. A statistically significant increase in the intention to obtain clinical trial information at the three and six month time points was observed in the intervention group, but not the control group. Older participants (65–95 years) were less likely than younger participants (50–64 years) to increase their motivation to seek clinical trial information by the three and six month time points. No significant increases were observed in intention to join clinical trials. This randomized trial shows that AA church-based educational interventions are likely to increase the motivation of AA subjects to obtain clinical trial information and are therefore potentially effective at ameliorating the underrepresentation of AA subjects in clinical trials.
机译:这是一份关于一项随机分组临床试验的报告,该试验评估了基于教会的教育干预措施的有效性,该干预措施旨在提高非裔美国人(AA)参与临床试验。来自六个主要的AA教堂的221位年龄≥50岁的AA受试者被随机分配到干预或控制条件下。干预措施包括三期有关临床试验和健康差异的教育会议;对照参与者完成问卷。该研究的主要终点是个体受试者获得临床试验信息的意愿和参加临床试验的意愿的差异,这由基线,三个月和六个月时的10分量表确定。在干预组而非对照组中,在三个月和六个月的时间点上获得临床试验信息的意向在统计学上显着增加。年龄较大的参与者(65-95岁)比年龄较小的参与者(50-64岁)在三个月和六个月的时间点增加寻求临床试验信息的动力的可能性较小。参加临床试验的意图未见明显增加。这项随机试验表明,基于AA教会的教育干预措施可能会增加AA受试者获得临床试验信息的动机,因此有可能有效地改善AA受试者在临床试验中代表性不足的情况。

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