Randomization Inference in a Group–Randomized Trial of Treatments for Depression

In the Prospect Study, in 10 pairs of two primary-care practices, one practice was picked at random to receive a “depression care manager” to treat its depressed patients. Randomization inference, properly performed, reflects the assignment of practices, not patients, to treatment or control. Yet, pertinent data describe individual patients: depression outcomes, baseline covariates, compliance with treatment. The methods discussed use only (i) the random assignment of clusters to treatment or control and (ii) the hypothesis about effects being tested or inverted for confidence intervals, so they are randomization inferences in Fisher's strict sense. There is no assumption that the covariance model generated the data, that compliers resemble noncompliers, that dependence is from additive random cluster effects, that individuals in a same cluster do not interfere with one another, or that units are sampled from a population. We contrast methods of covariance adjustment, never assuming the models are “true,” obtaining exact randomization inferences. We consider exact inference about effects proportional to doses with noncompliance and effects whose magnitude varies with the degree of improvement that would occur without treatment. A simulation examines power.

[1]  J. Fleiss Statistical methods for rates and proportions , 1974 .

[2]  R. Glynn,et al.  Incorporation of Clustering Effects for the Wilcoxon Rank Sum Test: A Large‐Sample Approach , 2003, Biometrics.

[3]  R J Carroll,et al.  On design considerations and randomization-based inference for community intervention trials. , 1996, Statistics in medicine.

[4]  J. I The Design of Experiments , 1936, Nature.

[5]  Paul R Rosenbaum,et al.  Sensitivity Analysis for m‐Estimates, Tests, and Confidence Intervals in Matched Observational Studies , 2007, Biometrics.

[6]  J. Friedman,et al.  Projection Pursuit Regression , 1981 .

[7]  Xiao-Hua Zhou,et al.  Clustered encouragement designs with individual noncompliance: bayesian inference with randomization, and application to advance directive forms. , 2002, Biostatistics.

[8]  David M Murray,et al.  A comparison of permutation and mixed‐model regression methods for the analysis of simulated data in the context of a group‐randomized trial , 2006, Statistics in medicine.

[9]  Joshua D. Angrist,et al.  Identification of Causal Effects Using Instrumental Variables , 1993 .

[10]  R. Tibshirani,et al.  Linear Smoothers and Additive Models , 1989 .

[11]  N Mantel,et al.  Ranking procedures for arbitrarily restricted observation. , 1967, Biometrics.

[12]  E. Pitman SIGNIFICANCE TESTS WHICH MAY BE APPLIED TO SAMPLES FROM ANY POPULATIONS III. THE ANALYSIS OF VARIANCE TEST , 1938 .

[13]  Terence P. Speed,et al.  Introductory Remarks on Neyman (1923) , 1990 .

[14]  W. Grove Statistical Methods for Rates and Proportions, 2nd ed , 1981 .

[15]  P. Rosenbaum,et al.  Reduced Sensitivity to Hidden Bias at Upper Quantiles in Observational Studies with Dilated Treatment Effects , 1999, Biometrics.

[16]  D. Jacobs,et al.  PARAMETERS TO AID IN THE DESIGN AND ANALYSIS OF COMMUNITY TRIALS: INTRACLASS CORRELATIONS FROM THE MINNESOTA HEART HEALTH PROGRAM , 1994, Epidemiology.

[17]  B. L. Welch ON THE z-TEST IN RANDOMIZED BLOCKS AND LATIN SQUARES , 1937 .

[18]  Dechang Chen,et al.  The Theory of the Design of Experiments , 2001, Technometrics.

[19]  D. Rubin Comment: Which Ifs Have Causal Answers , 1986 .

[20]  P Diehr,et al.  Selected statistical issues in group randomized trials. , 2001, Annual review of public health.

[21]  E. Glaser The randomized clinical trial. , 1972, The New England journal of medicine.

[22]  Kjell A. Doksum,et al.  Plotting with confidence: Graphical comparisons of two populations , 1976 .

[23]  M. H. Gail,et al.  Tests for no treatment e?ect in randomized clinical trials , 1988 .

[24]  D. DeMets,et al.  The randomized clinical trial: bias in analysis. , 1981, Circulation.

[25]  P Elterenvan On the combination of independent two-sample tests of wilcoxon , 1960 .

[26]  Thomas R Ten Have,et al.  Reducing suicidal ideation and depressive symptoms in depressed older primary care patients: a randomized controlled trial. , 2004, JAMA.

[27]  F. Ingelfinger The randomized clinical trial. , 1972, The New England journal of medicine.

[28]  R. Glynn,et al.  Extension of the Rank Sum Test for Clustered Data: Two‐Group Comparisons with Group Membership Defined at the Subunit Level , 2006, Biometrics.

[29]  Paul R. Rosenbaum,et al.  Robust, accurate confidence intervals with a weak instrument: quarter of birth and education , 2005 .

[30]  I NICOLETTI,et al.  The Planning of Experiments , 1936, Rivista di clinica pediatrica.

[31]  D. Rubin [On the Application of Probability Theory to Agricultural Experiments. Essay on Principles. Section 9.] Comment: Neyman (1923) and Causal Inference in Experiments and Observational Studies , 1990 .

[32]  E. Lehmann Testing Statistical Hypotheses , 1960 .

[33]  D. Rubin Estimating causal effects of treatments in randomized and nonrandomized studies. , 1974 .

[34]  David M. Murray,et al.  Design and Analysis of Group- Randomized Trials , 1998 .

[35]  P. Rosenbaum,et al.  Randomization Inference With Imperfect Compliance in the ACE-Inhibitor After Anthracycline Randomized Trial , 2004 .

[36]  E. Pitman Significance Tests Which May be Applied to Samples from Any Populations , 1937 .

[37]  P. Rosenbaum Covariance Adjustment in Randomized Experiments and Observational Studies , 2002 .

[38]  Efficiency of the Wilcoxon Two-Sample Statistic for Randomized Blocks , 1963 .

[39]  R Brookmeyer,et al.  Person-time analysis of paired community intervention trials when the number of communities is small. , 1998, Statistics in medicine.

[40]  Jonathan Raz,et al.  Testing for No Effect When Estimating a Smooth Function by Nonparametric Regression: A Randomization Approach , 1990 .

[41]  Ziding Feng,et al.  Optimal Permutation Tests for the Analysis of Group Randomized Trials , 2001 .