Research fundamentals: Follow-up of subjects in clinical trials: Addressing subject attrition

被引:47
作者
Woolard, RH
Carty, K
Wirtz, P
Longabaugh, R
Nirenberg, TD
Minugh, PA
Becker, B
Clifford, PR
机构
[1] Brown Univ, Rhode Isl Hosp, Sch Med, Dept Emergency Med, Providence, RI 02903 USA
[2] Brown Univ, Sch Med, Ctr Alcohol & Addict Studies, Providence, RI 02912 USA
[3] George Washington Univ, Dept Management Sci, Washington, DC USA
[4] George Washington Univ, Dept Psychol, Washington, DC USA
[5] Brown Univ, Rhode Isl Hosp, Sch Med, Injury Prevent Ctr,Ctr Alcohol & Addict Studies, Providence, RI 02903 USA
[6] Datacorp, Providence, RI USA
[7] NYU, Dept Hlth Studies, New York, NY USA
基金
美国国家卫生研究院;
关键词
attrition; follow-up; research methodology; alcohol; intoxication; injury prevention; missing data;
D O I
10.1197/j.aem.2003.09.021
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Many published clinical trials have less than adequate follow-up. When conducting a clinical trial, researchers attempt to minimize data loss; however, some data may not be collected, particularly when subjects are lost to follow-up. Careful planning of research protocols, including comprehensive initial data collection, identification of locators, flexible scheduling, systematic subject tracking, monitoring subject loss, and systematically approaching problem cases can ensure high follow-up rates. This article presents a compendium of techniques and procedures that researchers can use to enhance follow-up and address attrition in their studies. Finally, this article outlines statistical techniques that can be used to address the effects of missing data, particularly when patients are lost to follow-up.
引用
收藏
页码:859 / 866
页数:8
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