Handling missing data in longitudinal clinical trials: three examples from the pediatric psychology literature

被引:0
|
作者
Peugh, James [1 ,2 ]
Mara, Constance [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Behav Med Clin Psychol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
关键词
clinical trial; longitudinal research; statistical approach; randomized controlled trial; GENERALIZED ESTIMATING EQUATIONS; FULLY CONDITIONAL SPECIFICATION; MULTIPLE IMPUTATION; MAXIMUM-LIKELIHOOD; MULTILEVEL MODELS; VARIANCE; REGRESSION; EFFICIENCY; RESPONSES; STRATEGY;
D O I
10.1093/jpepsy/jsae070
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Researchers by default tend to choose complex models when analyzing nonindependent response variable data, this may be particularly applicable in the analysis of longitudinal trial data, possibly due to the ability of such models to easily address missing data by default. Both maximum-likelihood (ML) estimation and multiple imputation (MI) are well-known to be acceptable methods for handling missing data, but much of the recently published quantitative literature has addressed questions regarding the research designs and circumstances under which one should be chosen over the other. The purpose of this article is threefold. First, to clearly define the assumptions underlying three common longitudinal trial data analysis models for continuous dependent variable data: repeated measures analysis of covariance (RM-ANCOVA), generalized estimating equation (GEE), and a longitudinal linear mixed model (LLMM). Second, to clarify when ML or MI should be chosen, and to introduce researchers to an easy-to-use, empirically well-validated, and freely available missing data multiple imputation program: BLIMP. Third, to show how missing longitudinal trial data can be handled in the three data analysis models using three popular statistical analysis software packages ( SPSS , Stata, and R ) while keeping the published quantitative research in mind.
引用
收藏
页数:25
相关论文
共 50 条
  • [1] Review of guidelines and literature for handling missing data in longitudinal clinical trials with a case study
    Liu, M
    Wei, L
    Zhang, J
    PHARMACEUTICAL STATISTICS, 2006, 5 (01) : 7 - 18
  • [2] A review of the handling of missing longitudinal outcome data in clinical trials
    Matthew Powney
    Paula Williamson
    Jamie Kirkham
    Ruwanthi Kolamunnage-Dona
    Trials, 15
  • [3] A review of the handling of missing longitudinal outcome data in clinical trials
    Powney, Matthew
    Williamson, Paula
    Kirkham, Jamie
    Kolamunnage-Dona, Ruwanthi
    TRIALS, 2014, 15
  • [4] A tutorial for handling suspected missing not at random data in longitudinal clinical trials
    Peugh, James
    Toland, Michael
    Harrison, Heather
    QUANTITATIVE METHODS FOR PSYCHOLOGY, 2023, 19 (04): : 347 - 367
  • [5] Handling missing data in clinical trials: An overview
    Myers, WR
    DRUG INFORMATION JOURNAL, 2000, 34 (02): : 525 - 533
  • [6] Handling Missing Data in Clinical Trials: An Overview
    William R. Myers
    Drug information journal : DIJ / Drug Information Association, 2000, 34 (2): : 525 - 533
  • [7] Handling missing data issues in clinical trials for rheumatic diseases
    Wong, Weng Kee
    Boscardin, W. J.
    Postlethwaite, A. E.
    Furst, D. E.
    CONTEMPORARY CLINICAL TRIALS, 2011, 32 (01) : 1 - 9
  • [8] Commentary: Indefensible Methods of Handling Missing Data in Clinical Trials
    Arndt, Stephan
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2013, 37 (12) : 1997 - 1998
  • [9] AN OVERVIEW OF PRACTICAL APPROACHES FOR HANDLING MISSING DATA IN CLINICAL TRIALS
    DeSouza, Cynthia M.
    Legedza, Anna T. R.
    Sankoh, Abdul J.
    JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2009, 19 (06) : 1055 - 1073
  • [10] MISSING DATA HANDLING METHODS IN MEDICAL DEVICE CLINICAL TRIALS
    Yan, Xu
    Lee, Shiowjen
    Li, Ning
    JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2009, 19 (06) : 1085 - 1098