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临床研究中特殊人群的纳入:重要考量与指南

Inclusion of special populations in clinical research: important considerations and guidelines.

作者信息

Winter Stuart S, Page-Reeves Janet M, Page Kimberly A, Haozous Emily, Solares Angelica, Nicole Cordova Carla, Larson Richard S

机构信息

Children's Minnesota Research Institute, Minneapolis, MN, United States.

Department of Family and Community Medicine, University of New Mexico, Albuquerque, United States.

出版信息

J Clin Transl Res. 2018 Apr 7;4(1):56-69. eCollection 2018 May 28.

PMID:30873495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6410628/
Abstract

BACKGROUND

Trials that involve human participants call for experiments or observations that are performed in a clinical research setting. Currently, there are over 16,000 clinical trials open in the United States. Despite continuing efforts to include "special populations" in clinical trials, there are gaps in participation for people who are either minors or elderly adults, are from historically under-represented minorities, or live in rural communities. The inclusion of these special populations in clinical trials research is essential for conclusions that benefit all populations. Data suggest that study partic-ipation rates for special populations have fallen to levels that could endanger the successful performance of some types of research. This is particularly concerning in the 21st century, where demographic trends in the United States continue to shift towards an older and Hispanic population with fewer rural dwellers. Trends in New Mexico and other minority-majority states mirror many of these shifts.

RELEVANCE FOR PATIENTS

In this review, we highlight improvement strategies for enhanced clinical trial participation by members of special populations. Key drivers for disparate clinical trials participation and outcomes often include differences in genetics, physiology, and perceptions of mistrust towards researchers. To overcome these barriers, we focus on best practices in recruitment strategies from the perspectives of the participants, the researchers and the institutions that support clinical trials.

摘要

背景

涉及人类参与者的试验需要在临床研究环境中进行实验或观察。目前,美国有超过16000项临床试验正在进行。尽管一直在努力将“特殊人群”纳入临床试验,但在未成年人、老年人、历史上代表性不足的少数群体或农村社区居民的参与方面仍存在差距。将这些特殊人群纳入临床试验研究对于得出惠及所有人群的结论至关重要。数据表明,特殊人群的研究参与率已降至可能危及某些类型研究成功开展的水平。在21世纪,美国的人口趋势继续朝着老年化和西班牙裔人口方向转变,农村居民减少,这一点尤其令人担忧。新墨西哥州和其他少数族裔占多数的州的趋势反映了其中许多变化。

对患者的相关性

在本综述中,我们强调了提高特殊人群成员临床试验参与度的改进策略。临床试验参与度和结果存在差异的关键驱动因素通常包括遗传学、生理学以及对研究人员不信任感方面的差异。为克服这些障碍,我们从参与者、研究人员以及支持临床试验的机构的角度,关注招募策略中的最佳实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254f/6410628/c203c8092e5e/jclintranslres-4-056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254f/6410628/274df038c85d/jclintranslres-4-056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254f/6410628/c203c8092e5e/jclintranslres-4-056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254f/6410628/274df038c85d/jclintranslres-4-056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254f/6410628/c203c8092e5e/jclintranslres-4-056-g002.jpg

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