Presentation is loading. Please wait.

Presentation is loading. Please wait.

Effect Sizes for Meta-analysis of Single-Subject Designs S. Natasha Beretvas University of Texas at Austin.

Similar presentations


Presentation on theme: "Effect Sizes for Meta-analysis of Single-Subject Designs S. Natasha Beretvas University of Texas at Austin."— Presentation transcript:

1 Effect Sizes for Meta-analysis of Single-Subject Designs S. Natasha Beretvas University of Texas at Austin

2 Beretvas grant Three studies: 1.a) Summarize practices used for meta- analyzing SSD results 1.b) Summarize methods used to calculate effect sizes (ESs) for SSD results 2. Simulation study evaluating performance of selection of ESs 3.Conduct actual meta-analysis of school-based interventions for children with autism spectrum disorders.

3 Outline Large-n designs’ data Large-n Effect Sizes Single-n designs’ data Single-n Effect Sizes (sample) Problems 4-parameter model (AB designs) Explanation Continuing research

4 Large-n Studies’ Data Most simply: consists of a randomly selected and assigned sample of participants in each of the Treatment and Control groups. Each participant is measured once on the outcome. Each participant provides an independently observed data point. The standard deviation provides an estimate of the variability of these independent data points.

5 Large-n Effect Sizes Provides a practical measure of the size and direction of a treatment’s effect. In large-n studies, the standardized mean difference is most typically used: Represents how different the two groups’ means are on the outcome of interest. The “standardized” part originates in the difference being measured in standard deviations:

6 Single-n Studies’ Data

7 Most simply: repeated measures on an individual over time in two phases (time series data): Baseline: phase A = “control” Treatment: phase B = “treatment” Score at time point t is related to score at time (t – 1): not independent.

8 Single-n Studies’ Data Visual Analysis: Plots are evaluated for the presence of a treatment effect by simultaneously considering the following : Sustainable level and/or trend changes Baseline trends in expected direction Overlapping data between phases Variability changes within and across phases.

9 Single-n Effect Sizes Seems reasonable that a standardized difference between scores in phase A and B could be used as an effect size (ES): It seems feasible that this effect size would be on the same metric as for large-n designs?! No!!

10 Problems with d for single-n designs The standard deviation, s, for single-n designs describes different variability than for large-n designs. If these were not problems, then it would also only make sense to use d when there is no trend in the data.

11 Trend in A and B phases, tx effect A single number cannot summarize changes in level and slope

12 Trend in B phase, tx effect

13 Trend in A and B phases, no tx effect What would d indicate about this pattern?

14 Alternative single-n ESs Percent Non-overlapping data (PND) is one of the most frequently used ES descriptors. If treatment’s effect is anticipated to increase outcome then: Horizontal line drawn through highest point in phase A through points in phase B PND = % of phase B points above line The higher the PND, the stronger the support for a treatment’s effect.

15 PND PND = 6/6 = 100% BaselineTreatment

16 PND BaselineTreatment PND = 11/13 = 84.6%

17 PND PND is simple to calculate and interpret and takes into consideration: Baseline variability Slope changes, but

18 PND What would PND indicate about this pattern?

19 Alternative single-n ESs Assuming linear trends, it seems that two ESs should be used to describe change in level and trend. Huitema and McKean (2000) suggested using a four-parameter regression model (extension of piecewise reg’n suggested by Gorman and Allison, 1996). Appropriate parameterization of this model provides two coefficients that can be used to describe change in intercept and in slope from phase to phase:

20 4-parameter model The model: where Y t = outcome score at time t T t = time point D = phase (A or B) n 1 = # time points in phase A

21 4-parameter model – interpretation Coefficients represent the following:  0 = baseline intercept (i.e. Y at time = 0)  1 = baseline linear trend (slope over time)  2 = difference in intercept predicted from treatment phase data from that predicted for time = n 1 +1 from baseline phase data  3 = difference in slope Thus  2 and  3 provide estimates of a treatment’s effect on level and on slope, respectively.

22 4-parameter model - interpretation

23

24

25 22

26 4-parameter model Model can be estimated using OLS or autoregression (to correct SEs if residuals are autocorrelated). The four-parameter model can be expanded for ABAB designs. Multiple baseline designs can be thought of as multiple dependent, within-study AB designs.  2 and  3 can be calculated for each individual and then summarized across individuals for a study.

27 4-parameter model How does estimation of these coefficients function for differing true coefficient values? How does an omnibus test work? F-ratio testing addition of both predictors (with coefficients  2 and  3 ) How to standardize regression coefficients for meta-analytic synthesis? No procedure yet established for regular regression. Comparison with long list of other SSD ESs.


Download ppt "Effect Sizes for Meta-analysis of Single-Subject Designs S. Natasha Beretvas University of Texas at Austin."

Similar presentations


Ads by Google