Effect Sizes for Meta-analysis of Single-Subject Designs - PowerPoint PPT Presentation

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Effect Sizes for Meta-analysis of Single-Subject Designs

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Title: Meta-analysis of Single-Subject Designs Author: Tasha Beretvas Last modified by: sheryl.lazarus Created Date: 6/5/2006 3:56:33 PM Document presentation format – PowerPoint PPT presentation

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Title: Effect Sizes for Meta-analysis of Single-Subject Designs


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 treatments 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
Single-n Studies Data
  • 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 DataVisual 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 treatments 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 treatments effect.

15
PND
Baseline
Treatment
PND 6/6 100
16
PND
Baseline
Treatment
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 regn 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
  • Yt outcome score at time t
  • Tt time point
  • D phase (A or B)
  • n1 time points in phase A

21
4-parameter model interpretation
  • Coefficients represent the following
  • b0 baseline intercept (i.e. Y at time 0)
  • b1 baseline linear trend (slope over time)
  • b2 difference in intercept predicted from
    treatment phase data from that predicted for time
    n11 from baseline phase data
  • b3 difference in slope
  • Thus b2 and b3 provide estimates of a treatments
    effect on level and on slope, respectively.

22
4-parameter model - interpretation
23
4-parameter model - interpretation
24
4-parameter model - interpretation
25
4-parameter model - interpretation
b2
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.
  • b2 and b3 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 b2 and b3)
  • How to standardize regression coefficients for
    meta-analytic synthesis?
  • No procedure yet established for regular
    regression.
  • Comparison with long list of other SSD ESs.
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