针对服务不足人群的儿科临床研究试验招募:努力与挑战

K. Ireland, A. Manders, B. Corkey, C. Lenders
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引用次数: 3

摘要

简介:描述儿科临床试验招募的困难,目标是服务不足的儿童肥胖人群。方法:我们计划了一项为期6个月的随机、双盲、安慰剂对照的谷氨酰胺与安慰剂临床试验,以减少肥胖青少年的HOMA_IR和体重增加。参与者需要在上午8点到研究中心进行5次访问。参观时提供现金奖励。在招募困难之后,我们修改了研究设计,并在14周的时间内加强了招募工作。研究对象从波士顿医学中心(BMC)的儿科门诊诊所招募,包括由研究小组成员组成的儿科肥胖项目(NFL)。结果:对2002名青少年进行了评估,其中546名符合BMI和年龄标准。在进一步排除后,179人有资格进行筛查访问,但只有4人参加了。此外,向NFL患者发送了120封招募信,其中4人参加了筛查访问。参加筛查访问的8名青少年中有7名来自NFL, 2名被随机分组,但随后失去了随访。讨论:从BMC低收入和少数民族人群中招募儿科患者进行临床试验是困难的。挑战包括严格的纳入/排除标准和严格的预约时间表。现有的医患关系可能会增加招聘。未来的试验应采用更灵活的研究设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recruitment in a Pediatric Clinical Research Trial Targeting UnderservedPopulations: Efforts and Challenges
Introduction: To describe recruitment difficulties in a pediatric clinical trial targeting underserved pediatric obese populations. Methods: We planned a 6-month randomized, double-blind, placebo-controlled clinical trial of glutamine vs. placebo, to reduce HOMA_IR and weight gain in obese adolescents. Participation required 5 visits at a research center at 8:00 AM. Cash incentives were provided at visits. After recruitment difficulties, study design was modified and recruitment efforts were intensified over a 14-week period. Subjects were recruited from Boston Medical Center’s (BMC) pediatric outpatient clinics including the pediatric obesity program (NFL) which was staffed by members of the research team. Results: 2002 adolescents were evaluated: 546 met BMI and age criteria. After further exclusions, 179 were eligible for a screening visit but only 4 attended. Additionally, 120 recruitment letters were sent to NFL patients, resulting in 4 attending a screening visit. Seven of the 8 adolescents attending a screening visit were from NFL, and 2 were randomized but subsequently lost to follow-up. Discussion: Recruitment of pediatric patients from low-income and minority populations at BMC to a clinical trial is difficult. Challenges included strict inclusion/exclusion criteria and rigid appointment schedules. Existing patientclinician relationships may increase recruitment. Future trials should use more flexible study designs.
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