Performing high-powered studies efficiently with sequential analyses

被引:269
作者
Lakens, Daniel [1 ]
机构
[1] Eindhoven Univ Technol, Human Technol Interact Grp, IPO 1-33,POB 513, NL-5600 MB Eindhoven, Netherlands
关键词
SAMPLE-SIZE; REPLICATION; BOUNDARIES; DESIGN;
D O I
10.1002/ejsp.2023
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Running studies with high statistical power, while effect size estimates in psychology are often inaccurate, leads to a practical challenge when designing an experiment. This challenge can be addressed by performing sequential analyses while the data collection is still in progress. At an interim analysis, data collection can be stopped whenever the results are convincing enough to conclude that an effect is present, more data can be collected, or the study can be terminated whenever it is extremely unlikely that the predicted effect will be observed if data collection would be continued. Such interim analyses can be performed while controlling the Type 1 error rate. Sequential analyses can greatly improve the efficiency with which data are collected. Additional flexibility is provided by adaptive designs where sample sizes are increased on the basis of the observed effect size. The need for pre-registration, ways to prevent experimenter bias, and a comparison between Bayesian approaches and null-hypothesis significance testing (NHST) are discussed. Sequential analyses, which are widely used in large-scale medical trials, provide an efficient way to perform high-powered informative experiments. I hope this introduction will provide a practical primer that allows researchers to incorporate sequential analyses in their research. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:701 / 710
页数:10
相关论文
共 36 条
  • [21] Aggregate and Individual Replication Probability Within an Explicit Model of the Research Process
    Miller, Jeff
    Schwarz, Wolf
    [J]. PSYCHOLOGICAL METHODS, 2011, 16 (03) : 337 - 360
  • [22] Research Practices That Can Prevent an Inflation of False-Positive Rates
    Murayama, Kou
    Pekrun, Reinhard
    Fiedler, Klaus
    [J]. PERSONALITY AND SOCIAL PSYCHOLOGY REVIEW, 2014, 18 (02) : 107 - 118
  • [23] Registered Reports A Method to Increase the Credibility of Published Results
    Nosek, Brian A.
    Lakens, Daniel
    [J]. SOCIAL PSYCHOLOGY, 2014, 45 (03) : 137 - 141
  • [24] WHEN TO STOP A CLINICAL-TRIAL
    POCOCK, SJ
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 1992, 305 (6847): : 235 - 240
  • [25] GROUP SEQUENTIAL METHODS IN DESIGN AND ANALYSIS OF CLINICAL-TRIALS
    POCOCK, SJ
    [J]. BIOMETRIKA, 1977, 64 (02) : 191 - 200
  • [26] Proschan MA, 2006, STAT BIOL HEALTH, P1
  • [27] Computations for group sequential boundaries using the Lan-DeMets spending function method
    Reboussin, DM
    DeMets, DL
    Kim, K
    Lan, KKG
    [J]. CONTROLLED CLINICAL TRIALS, 2000, 21 (03): : 190 - 207
  • [28] At what sample size do correlations stabilize?
    Schoenbrodt, Felix D.
    Perugini, Marco
    [J]. JOURNAL OF RESEARCH IN PERSONALITY, 2013, 47 (05) : 609 - 612
  • [29] Simmons J., 2013, NA - Advances in Consumer Research, V41, DOI DOI 10.2139/SSRN.2205186
  • [30] False-Positive Psychology: Undisclosed Flexibility in Data Collection and Analysis Allows Presenting Anything as Significant
    Simmons, Joseph P.
    Nelson, Leif D.
    Simonsohn, Uri
    [J]. PSYCHOLOGICAL SCIENCE, 2011, 22 (11) : 1359 - 1366