Case Design

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From the article provided, answer the following questions.  

In your post, include the following:

1. Point out the experimental question & purpose of study. 

2. Point out the exact design utilized (example: non-concurrent multiple baseline) 

3. Think about the visual display of data and describe the (each):

o Level 

o Trend 

o Variability

o Latency to change

4. Shortly summarise if the study showed control & evidence to support your decision .

Modeling external events in the three-level analysis
of multiple-baseline across-participants designs:
A simulation study

Mariola Moeyaert & Maaike Ugille &
John M. Ferron & S. Natasha Beretvas &
Wim Van den Noortgate

Published online: 12 December 2012
# Psychonomic Society, Inc. 2012

Abstract In this study, we focus on a three-level meta-
analysis for combining data from studies using multiple-
baseline across-participants designs. A complicating factor
in such designs is that results might be biased if the depen-
dent variable is affected by not explicitly modeled external
events, such as the illness of a teacher, an exciting class
activity, or the presence of a foreign observer. In multiple-
baseline designs, external effects can become apparent if
they simultaneously have an effect on the outcome score
(s) of the participants within a study. This study presents a
method for adjusting the three-level model to external
events and evaluates the appropriateness of the modified
model. Therefore, we use a simulation study, and we illus-
trate the new approach with real data sets. The results
indicate that ignoring an external event effect results in
biased estimates of the treatment effects, especially when

there is only a small number of studies and measurement
occasions involved. The mean squared error, as well as the
standard error and coverage proportion of the effect esti-
mates, is improved with the modified model. Moreover, the
adjusted model results in less biased variance estimates. If
there is no external event effect, we find no differences in
results between the modified and unmodified models.

Keywords Multiple baseline across participants . Three-level
meta-analysis . Effect sizes . External event effect

A multiple-baseline design (MBD) is one of the variants of
single-subject experimental designs (SSEDs). SSED
researchers observe and measure a participant or case re-
peatedly over time. Observations are obtained during at least
one baseline phase (when no intervention is present) and at
least one treatment phase (when an intervention is present).
By comparing scores from both kinds of phases, SSED
researchers can assess whether the outcome scores on the
dependent variable changed, for instance, in level or in slope
when the treatment was present (Onghena & Edgington,
2005).

In an MBD, an AB phase design (with one baseline phase,
A, and one treatment phase, B) is implemented simultaneously
to different participants, behaviors, or settings (Barlow &
Hersen, 1984; Ferron & Scott, 2005; Onghena, 2005; Onghena
& Edgington, 2005). MBDs are popular among SSED
researchers (Shadish & Sullivan, 2011) because the interven-
tion is introduced sequentially over the participants (or settings
and behaviors), which entails the advantage that the researchers
can more easily disentangle effects of the intervention and
effects of some external events, such as the illness of a teacher,
an exciting class activity, the presence of a foreign observer, or

M. Moeyaert : M. Ugille
University of Leuven,
Leuven, Belgium

J. M. Ferron
University of South Florida,
Tampa, FL, USA

S. N. Beretvas
University of Texas,
Austin, TX, USA

W. Van den Noortgate
University of Leuven,
Leuven, Belgium

M. Moeyaert (*)
Faculty of Psychology and Educational Sciences,
University of Leuven,
Andreas Vesaliusstraat 2, Box 3762, 3000 Leuven, Belgium
e-mail: [email protected]

Behav Res (2013) 45:547–559
DOI 10.3758/s13428-012-0274-1

a teacher intern (Baer, Wolf, & Risley, 1968; Barlow & Hersen,
1984; Kinugasa, Cerin, & Hooper, 2004; Koehler & Levin,
2000). This is because, if an external event occurs at certain
points in time, the outcome scores for all participants in that
study might be simultaneously influenced. Figure 1 gives a
graphical presentation of possible consequences for the occur-
rence of an external event in a multiple-baseline across-
participants design. In Fig. 1a, the external event has a
constant effect on the dependent variable on subsequent
measurements—for instance, the teacher is ill during subse-
quent days, or there is a foreign observer during some measure-
ment occasions. Figure 1b illustrates a gradually fading away
external event effect. For instance, the influence of a teacher
intern on the behavior of the students may be reduced over time.

Van den Noortgate and Onghena (2003) proposed the use
of multilevel models to synthesize data from multiple SSED
studies, allowing investigation of the generalizability of the
results and exploration of potential moderating effects. In
previous research evaluating this multilevel meta-analysis of
MBD data (Ferron, Bell, Hess, Rendina-Gobioff, & Hibbard,
2009; Ferron, Farmer, & Owens, 2010; Moeyaert, Ugille,
Ferron, Beretvas, & Van den Noorgate, 2012a, 2012b; Owens
& Ferron, 2012), the data were typically simulated with
a treatment effect and random noise only. Potential

confounding events that could have a simultaneous ef-
fect on all participants within a study were not taken
into account. In this study, we evaluate the performance
of the basic three-level model when there are effects of
external events, as well as that of an extension of the
model that tries to account for potential event effects. In
the following, we first present the basic model and a
possible extension to account for external events. Next,
we evaluate the performance of both models, by means
of a simulation study and an analysis of real data.

Three-level meta-analysis

A meta-analysis combines the results of several studies
addressing the same research question (Cooper, 2010; Glass,
1976). Study results are typically first converted to a com-
mon standardized effect size before meta-analyzing them.
The effect sizes may be reported in the primary studies or
can be calculated afterward, using reported summary and/or
test statistics.

One possible way to calculate effect sizes when SSEDs
are used is to analyze the data using regression models and
to use the regression coefficients as effect sizes. A

Fig. 1 Graphical display of a constant external event effect (a) and a
gradually fading away external event effect (b) affecting the score on
four subsequent moments (day 17, day 19, day 21, and day 23) for a

multiple-baseline design across 3 participants, with the treatment start-
ing on day 6, day 16, and day 24, respectively

548 Behav Res (2013) 45:547–559

regression model of interest here is the one proposed by
Center, Skiba, and Casey (1985–1986):

Yi ¼ b0 þ b1Ti þ b2Di þ b3T 0iDi þ ei: ð1Þ

The score of the dependent variable on measurement
occasion i (Yi ) depends on a dummy coded variable (Di)
indicating whether the measurement occasion i belongs to
the baseline phase (Di 0 0) or the treatment phase (Di 0 1); a
time-related variable Ti that equals 1 on the first measure-
ment occasion of the baseline phase; and an interaction term
between the centered time indicator and the dummy vari-
able, T 0iDi, where T

0
i is centered such that T

0
i equals 0 on the

first measurement occasion of the treatment phase. b0 indi-
cates the expected baseline level b1 is the linear trend during
the baseline, b2 refers to the immediate treatment effect, and
b3 refers to the effect of the treatment on the time trend.

Van den Noortgate and Onghena (2003) proposed using
the ordinary least squares estimates for b2 and b3 from Eq. 1
as effect sizes in the three-level meta-analysis. At the first
level, the estimated effect sizes of the immediate treatment
effect, b2jk, and the treatment effect on the time trend, b3jk,
for participant j from study k are equal to the unknown
population effect sizes, β2jk and β3jk, respectively, plus ran-
dom deviation s,r2jk and r3jk, that are assumed to be normal-
ly distributed with a mean of zero:

b2jk ¼ b2jk þ r2jk with r2jk � N 0; σ2r2jk
� �

b3jk ¼ b3jk þ r3jk with r2jk � N 0; σ2r3jk
� �

:
ð2Þ

The sampling variances of the observed effects, σ2r2jk and

σ2r3jk ; are the squared standard errors that are typically

reported by default when a regression analysis is performed.
These variances depend to a large extent on the number of
observations and the variance of these observations and,
therefore, can be participant and study specific. At the
second level, the population effect sizes b2jk and b3jk from
Eq. 2 can be modeled as varying over participants around
the study-specific mean effect, θ20k and θ30k (Eq. 3):

b2jk ¼ θ20k þ u2jk with u2jk � N 0; σ2u2jk
� �

b3jk ¼ θ30k þ u3jk with u3jk � N 0; σ2u3jk
� �

:
ð3Þ

The population effects for studies can vary between studies
(third level, Eq. 4):

θ20k ¼ g200 þ v20k with v20k � N 0; σ2v20k
� �

θ30k ¼ g300 þ v30k with v30k � N 0; σ2v30k
� �

:
ð4Þ

The model parameters that we are typically interested in
when using a multilevel model are the fixed effects regression
coefficients (i.e., g200 , referring to the average immediate
treatment effect over participants and studies, and g300, refer-
ring to the average treatment effect on the linear trend over
participants and studies in Eq. 4) and the variances (i.e., σ2v20k ,

referring to the between-study variance for the estimated im-
mediate treatment effect; σ2v30k , indicating the between-study

variance for the estimated treatment effect on the time trend;
σ2u2jk , the between-case variance for the estimated immediate

treatment effect; and σ2u3jk , referring to the between-case vari-

ance of the estimated treatment effect on the time trend).

Correcting effect sizes for external events

External events in a multiple-baseline across-participants de-
sign can have an effect on the outcome score(s) of all partici-
pants within a study. These external event effects are common
in SSEDs, because practitioners often implement these designs
in their everyday setting (for example, in the home, school,
etc.), where they cannot control for outside experimental factors
(Christ, 2007; Kratochwill et al., 2010; Shadish, Cook, &
Campbell, 2002). If we do not model these external events,
the results might be biased. For instance, suppose that a re-
searcher is interested in a change in challenging behavior and
staggers the beginning of the treatment across 3 participants.
The 3 participants receive the treatment at day 6, day 16, and
day 24, respectively (see Fig. 1) and are observed every 2 days.
On days 17, 19, 21, and 23, the teacher is ill, and as a conse-
quence, a substitute teacher takes his or her place, and the
participants exhibit more challenging behavior. In this situation,
the estimated treatment effect for participants 1 and 2 will be
smaller, and the estimated treatment effect for participant 3 will
be larger, and therefore differences between participants in the
treatment effects are also likely to be overestimated, unless we
correct the effect sizes for possible external events.

A possible way to calculate effect sizes corrected for an
external event in an SSED is by estimating effect sizes for
participants per study, by performing a regression analysis
with a model including possible event effects, and by as-
suming that external events simultaneously affect all partic-
ipants in a study. Thereafter, the corrected effect sizes can be
combined over studies in the three-level meta-analysis.

For the first step, we propose to use an extension of the
Center et al. (1985–1986) model, including dummy varia-
bles for measurement occasions:

Yij ¼ b0j þ b1jTij þ b2jDij þ b3jDijT
0
ij

þ
XI�1
m¼2

b mþ2ð ÞMmi þ eij: ð5Þ

Behav Res (2013) 45:547–559 549

The score on the dependent variable Y on measurement
occasion i (0 1, 2, . . . , I) from participant j (0 1, 2, . . . , J) is
modeled as a linear function of the dummy-coded variable
(Dij) indicating whether the measurement occasion i from
participant j belongs to the baseline phase (Dij 0 0) or the
treatment phase (Dij 0 1); a time-related variable Tij, which
equals 1 at the start of the baseline phase; an interaction term
between the dummy variable indicating the phase and the
time indicator centered around its value at the start of the

treatment phase, DijT
0
ij; and finally, dummy-coded variables

indicating the moment (Mmi 0 1 if m 0 i, zero otherwise). By
including the effects of individual moments, coefficients β2j
and β3j can be interpreted as the treatment effects, corrected
for possible external events.

We do not include a dummy variable for one mea-
surement moment in the baseline phase and one mea-
surement moment in the treatment phase. This is to
ensure that the model is identified; if we included these
parameters as well, an increase in the effects for each
moment in the baseline phase could be compensated for
by a decrease of the intercept, illustrating that without
constraining these parameters, there would be an infinite
number of equivalent solutions. For our study, we select
the first and last moments as the times at which to set
the moment effects to zero, but different moments can
be chosen if we suspect a moment effect during one of
these times.

While the baseline level and slope (β0j and β1j) and both
treatment effects (β2j and β3j) are participant specific, the
moment effects are assumed to be the same for all partic-
ipants from the same study and, therefore, have to be esti-
mated for each study, using all data from that study. To this
end, we propose to extend Eq. 5 by including a set of
dummy participant indicators. For 2 participants, using
dummy participant indicators P1 and P2, respectively, this
results in Eq. 6:

Yij ¼ b01P1j þ b02P2j þ b11Ti1P1j þ b12Ti2P2j
þ b21Di1P1j þ b22Di2P2j þ b31Di1T

0
i1P1j

þ b32Di2T
0
i2P2j þ

XI�1
m¼2

b mþ2ð ÞMmi þ eij: ð6Þ

After using Eq. 6 for each study to estimate the
corrected effect sizes (β2j and β3j) for each participant,
we can use the three-level meta-analysis (see Eqs. 2–4)
to combine the corrected effect size estimates from
multiple participants. In principle, we could also use a
two-level model per study to estimate the participant-
specific effects, but given the typically very small num-
ber of participants per study, using a multilevel model
might not be recommended.

A simulation study

Simulating three-level data

To evaluate the performance of the basic model and its
extension, we performed a simulation study. We simulated
raw data using a three-level model. At level 1, we used the
following model:

Yijk ¼ b0jk þ b1jkTijk þ b2jkDijk þ b3jkTijkDijk þ eijk
with eijk � N 0; σ2e

� �
;

ð7Þ

with measurement occasions nested within participants,
which form the units at level two:

b0jk ¼ θ00k þ u0jk
b1jk ¼ θ10k þ u1jk
b2jk ¼ θ20k þ u2jk
b3jk ¼ θ30k þ u3jk

8>><
>>:

with

u0jk
u1jk
u2jk
u3jk

2
664

3
775 � N 0; @uð Þ: ð8Þ

The participants are, in turn, clustered within studies at
the third level:

θ00k ¼ g000 þ v00k
θ10k ¼ g100 þ v10k
θ20k ¼ g200 þ v20k
θ30k ¼ g300 þ v30k

8>><
>>:

with

v00k
v10k
v20k
v30k

2
664

3
775 � N 0; @vð Þ: ð9Þ

Varying parameters

On the basis of a thorough overview of 809 SSED studies,
Shadish and Sullivan (2011) enumerated some parameters
that characterize SSEDs. On the basis of their results and our
reanalyses of meta-analyses of SSEDs (Alen, Grietens, &
Van den Noortgate, 2009; Denis, Van den Noortgate, & Maes,
2011; Ferron et al., 2010; Kokina & Kern, 2010; Shadish &
Sullivan, 2011; Shogren, Faggella-Luby, Bae, & Wehmeyer,
2004; Wang, Cui, & Parrila, 2011), we decided to vary the
following parameters that can have a significant influence on
the quality of model estimation:

& g200 , represents the immediate treatment effect on the
outcome and had values 0 (no effect) or 2.

& The treatment effect on the time trend, defined by g300,
was varied to have values 0 (no effect) or 0.2.

& The regression coefficients of the baseline, g000 and
g100 , did not vary and were set at 0, because the
interest is in the overall treatment effects (e.g., the
immediate treatment effect and the treatment effect
on the time trend).

& The number of simulated participants, J, equaled 4 or 7.
& The number of measurements within a participant, I, was

15 or 30. We chose to keep I constant for all participants
within the same study.

550 Behav Res (2013) 45:547–559

& The number of studies, K, was 10 or 30.
& The between-case covariance matrix: Covariances between

pairs of regression coefficients were set to zero. Therefore,u

is a diagonal matrix:
P

u ¼ diag σ2u0; σ2u1; σ2u2; σ2u3
� �

¼
diag 2; 0:2; 2; 0:2ð Þ or Pu ¼ diag σ2u0; σ2u1; σ2u2; σ2u3

� �
¼

diag 0:5; 0:05; 0:5; 0:05ð Þ.
& The between-study covariance matrix: Covariances between

pairs of regression coefficients were set to zero. Therefore, v

is a diagonal matrix:
P

v ¼ diag σ2v0; σ2v1; σ2v; σ2v3
� �

¼
diag 2; 0:2; 2; 0:2ð Þ or Pv ¼ diag σ2v0; σ2v1; σ2v2; σ2v3

� �
¼

diag 0:5; 0:05; 0:5; 0:05ð Þ.
& The moment of introducing a treatment effect was stag-

gered across participants within a study (see Table 1),
depending on the number of measurements.

In a first scenario, a constant external event was added to
influence four subsequent scores of all the participants with-
in a study (as in Fig. 1a). The moment was randomly
generated from a uniform distribution for each study sepa-
rately. Because we did not include a moment effect for the
first and the last moments to make the model identified, the
external event effect did not occur on these moments. The
external event effect was 0 or 2, representing a null and a
large external event effect, respectively.

In a second scenario, the effect of the external event effect
was added, which fades away gradually (see Fig. 1b) for all
the participants within a study. The effect across four time
points was 3.5, 2.5, 1.5, 0.5, and 0, respectively, so that, on
average, the overall effect was the same as in the first scenario.
The start of the event effect was generated completely at
random from a uniform distribution for each study separately,
so that the external event effect did not occur on the first or last
measurement occasion. Data were generated using SAS.

Analysis

We had a total of 29 (0 512) experimental conditions. We
simulated 400 replications of each condition, resulting in
204,800 data sets to analyze. We analyzed the data twice and
compared the results. First, we combined the uncorrected effect
sizes in the three-level meta-analysis. Next, we analyzed the

three-level data by estimating the corrected effect sizes, β2j and
β3j, using the regression analysis per study (see Eq. 5) before
combining them in the three-level meta-analysis (see Eqs. 2–4).

In the two approaches, we used the SAS proc MIXED
(Littell, Milliken, Stroup, Wolfinger, & Schabenberger,
2006) procedure to estimate the participant-specific effect
sizes, β2jk and β3jk. In the first approach, the effect sizes
were uncorrected for the external event effect, whereas the
effect sizes in the second approach were corrected.

SAS proc MIXED was also used for the three-level meta-
analysis. The Satterthwaite approach to estimating the
degrees of freedom method was applied because this meth-
od provides more accurate confidence intervals for estimates
of the average treatment effect for two-level analyses of
multiple-baseline data (Ferron et al., 2009).

In order to evaluate the appropriateness of both models,
uncorrected and corrected for external events, we calculated
the deviations of the estimated immediate treatment effect,
bg200, from its population value, g200, and the deviations of the
estimated treatment effect on the time trend, bg300 , from its
population value,g300. The mean deviation gives us an idea of
the bias. Next, we calculated the mean squared deviation (the
mean squared error [MSE]), which gives information about
the variance of both estimated treatment effects (bg200 andbg300)
around the corresponding population effect (g200 and g300).
Furthermore, we discuss the standard error and the 95 %
confidence interval coverage proportion (CP) of the estimated
immediate treatment effect and the treatment effect on the time
trend. We also evaluate the bias of the point estimates of the
between-study and between-case variances.

We used ANOVAs to evaluate whether there were signifi-
cant effects (α 0 .01) of each model type (e.g., model using
effect sizes corrected vs. uncorrected for external event effects)
and of the simulation design parameters (g200, g300, K, I, J, σ

2
u2
,

σ2v2) on the bias, the MSE, the standard error, and the CP.

Results of the simulation study

We present the results in two sections. In the first section,
we discuss the constant external effect over four subsequent
measurement occasions. The second section considers the
case where the external effect gradually fades away over

Table 1 Time of introducing the treatment

Start of intervention

I Participant 1 Participant 2 Participant 3 Participant 4 Participant 5 Participant 6 Participant 7

15 5 6 7 8 9 11 13

30 5 8 11 14 17 20 23

Behav Res (2013) 45:547–559 551

four subsequent measurements. Each section presents the
results of the three-level analysis of uncorrected and cor-
rected effect sizes.

When there is no external event effect, the results of the
three-level meta-analysis (i.e., bias in the fixed effects, MSE
of the fixed effects, estimated standard errors of the fixed
effects, CP for the fixed effects, and bias in the variance
components) were found to be independent of the model
type (corrected or not corrected for external events).

We found no significant bias for bg200 and bg300 when using
the corrected or uncorrected model. Therefore, we discuss
the results of the analyses of the data including only external
event effects conditions.

Constant external event over four subsequent measurement
occasions

Overall treatment effect

Bias When we estimate g200 and the effect sizes are uncor-
rected, the estimated treatment effect is, on average, signifi-
cantly larger than the population value (g200 0 0 or 2). Over all
conditions, the bias equals 0.032, t(51199) 0 17.32, p < .0001,
whereas there is no significant bias for the corrected effect
sizes (−0.0015), t(51199) 0 −0.96, p 0 .34. Table 2 presents
the bias estimates for bg200, when g200 0 2 and g300 0 0.2.

Similar results are obtained for bg300. The bias is significantly
negative for the uncorrected effect sizes and equals −0.20,
t(51199) 0 −255.27, p < .0001, whereas the bias is not signif-
icant for the corrected effect sizes, t(51199) 0 −0.00020, p 0 .79.
Moreover, an analysis of variance on the deviations reveals a
significant difference between the two different models, for both
bg200 and bg300 [F(1, 102398) 0 192.06, p < .0001 for bg200, and F
(1, 102398) 0 33,695.1, p < .0001 for bg300�. The differences are
largest when there is a small number of measurement occasions
(I 0 15) and studies (K 0 10). In the following condition, the

largest difference was identified: g200 0 2, g300 0 0, K 0 10, I 0
15, J 0 4, σ2u2 0 0.5, and σ

2
v2
0 2 (with a difference of 0.23).

MSE Similar to the bias, the MSE of the estimated treatment
effect depends significantly on the model type; using an
analysis of variance on the squared deviations, F(1,
102398) 0 882.77, p < .0001 for bg200 and F(1, 102398) 0
7,076.91, p < .0001 for bg300 . When using the corrected
model, the MSE for bg200 and bg300 equals 0.12 and 0.028,
respectively, whereas it is 0.18 and 0.070, respectively, for
the uncorrected effect sizes. Differences between both mod-
els are larger if the number of observations and the number
of studies are small (see Table 3 for bg200; similar results are
obtained for bg300 ). So especially in these conditions, the
modified model is recommended.

Estimates of the standard errors In order to evaluate infer-
ences regarding the treatment effects, we constructed confidence
intervals around the estimated treatment effects, bg200 and bg300
Therefore, we needed to estimate the standard errors of the
estimated treatment effects. Because we obtained 400 estimates
of the effects in each condition, the standard deviations of the
effect estimates can be regarded as a relatively good estimate of
the standard deviation of the sampling distribution and can,
therefore, be used as a criterion to evaluate the standard error.
We looked at the relative standard error biases, which are the
differences between the median standard error estimates and the
standard deviation of the estimates of the effect divided by the
standard deviation of the estimates ofbg200 andbg300. The relative
differences are negative for bg200, which means that the median
standard error estimates are smaller than expected. For bg300 ,
these differences are positive, referring to median standard error
estimates larger than expected. The relative standard error biases
for both bg200 and bg300 are, on average, larger across the
conditions for the uncorrected effect sizes, in comparison with

Table 2 The bias of bg200 in the g200 0 2, and g300 0 0.2 conditions for the constant external event effect over four subsequent measurement occasions
Corrected Unorrected

I 0 15 I 0 30 I 0 15 I 0 30

K J σ2u2 σ
2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2

10 4 0.5 −0.003 0.007 0.025 −0.036 0.213 0.208 −0.027 0.027

2 0.015 0.002 −0.017 0.014 0.129 0.196 0.012 0.035

7 0.5 −0.026 −0.057 0.024 0.005 −0.093 −0.058 −0.019 −0.074

2 −0.028 −0.015 −0.011 −0.003 −0.099 −0.060 −0.016 −0.026

30 4 0.5 0.009 0.028 0.004 −0.005 0.219 0.185 −0.008 0.013

2 0.018 0.021 0.004 −0.011 0.210 0.222 0.008 0.035

7 0.5 0.023 0.005 0.002 −0.009 −0.075 −0.105 −0.004 −0.016

2 0.001 0.026 −0.006 −0.012 −0.077 −0.088 −0.003 0.006

“Corrected” and “uncorrected” refer, respectively, to corrected effect size and uncorrected effect size for external event effects

552 Behav Res (2013) 45:547–559

the corrected effect sizes. For bg200, the average relative standard
error biases equal −1.8 % and −2.0 % for the corrected and
uncorrected models, respectively. The average relative standard
error biases difference forbg300 for the uncorrected model is 2 %,
whereas it is substantial (more than 10 %; Hoogland &
Boomsma; 1998) for the uncorrected model (25.7 %). So the
difference between the model types becomes more apparent
when g300 is estimated, F(1, 254) 0 38.9, p < .0001. The
conditions with the largest relative standard error bias when
the uncorrected model for bg300 was used tended to coincidence
with the conditions where 30 studies, an immediate treatment
effect of 2, and a treatment effect on the time trend of 0.2 were
involved, with the bias mounting to 107 % in the condition
where g200 0 2, g300 0 0.2, K 0 30, J 0 7, I 0 30, σ

2
v2
0 0.5, and

σ2u2 0 0.5.

Coverage proportion We estimated the CP of the 95 % confi-
dence intervals, which allowed us to evaluate the interval esti-
mates of bg200 and bg300. The confidence intervals were estimated
by using the standard errors and the Satterthwaite estimated
degrees of freedom. The CP of these confidence intervals was
estimated for each of the combinations. A positive significant
difference between the corrected model and the uncorrected
model in the CP is found for bg200, F(1, 254) 0 27.56,
p < .0001 (see Table 4). Also, for bg300, the mean CP
depends significantly on the model type, F(1, 254) 0
20.96, p < .0001 (see Table 4). The conditions with a
CP less than .93 all have 15 measurements in common
and occur when the effect sizes are uncorrected, for
both bg200 and bg300. Moreover, for bg300, the CP is not
only too small when I 0 15 and K 0 30, but also too

Table 3 The MSE of bg200 in the g200 0 2, and g300 0 0.2 conditions for the constant external event effect over four subsequent measurement occasions
Corrected Unorrected

I 0 15 I 0 30 I 0 15 I 0 30

K J σ2u2 σ
2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2 σ

2
v2
0 0.5 σ2v2 0 2

10 4 0.5 0.17 0.28 0.11 0.26 0.32 0.43 0.14 0.25

2 0.20 0.32 0.14 0.28 0.31 0.49 0.16 0.36

7 0.5 0.09 0.24 0.07 0.23 0.18 0.31 0.09 0.22

2 0.11 0.26 0.09 0.24 0.20 0.31 0.09 0.28

30 4 0.5 0.06 0.10 0.04 0.09 0.14 0.19 0.04 0.10

2 0.06 0.11 0.04 0.09 0.15 0.20 0.05 0.12

7 0.5 0.03 0.07 0.03 0.08 0.06 0.10 0.03 0.09

2 0.04 0.08 0.03 0.08 0.07 0.10 0.04 0.08

“Corrected” and “uncorrected” refer, respectively, to corrected effect size and uncorrected effect size for external event effects

Table 4 The coverage proportion of bg200 and bg300 in the g200 0 2, g300 0 0.2, and σ2u2 0 2 conditions for the constant external event effect over four
subsequent measurement occasions

bg200 bg300
Corrected Uncorrected Corrected Uncorrected

K J σ2v2 I 0 15 I 0 30 I 0 15 I 0 30 I 0 15 I 0 30 I 0 15 I 0 30

10 4 0.5 .96 .96 .96 .96 .94 1.00 .97 1.00

2 .95 .95 .92 .95 .96 .98 .93 1.00

7 0.5 .96 .95 .94 .97 .99 1.00 .97 1.00

2 .97 .96 .95 .95 .96 .97 .84 .99

30 4 0.5 .97 .96 .89 .97 .97 1.00 .90 1.00

2 .97 .96 .91 .94 .96 .98 .49 1.00

7 0.5 .94 .94 .92 .96 .98 1.00 .93 1.00

2 .96 .95 .96 .96 .96 .97 .26 .96

Values smaller than .93 and larger than .97 appear in bold. “Corrected” and “uncorrected” refer, respectively, to corrected effect size and
uncorrected effect size for external event effects

Behav Res (2013) 45:547–559 553

large when I 0 30 (values for the CP range from .99 to
1.00). When the effect sizes are uncorrected, the CP is
well estimated when I 0 30 for bg200 and I 0 15 and K 0
10 for bg300. The difference in CP for bg200 is largest
when there is only a small number of measurements
(I 0 15) and a large number of studies (I 0 30).

Variance components

In the three-level analyses, the between-study and between-
case variances were estimated for both the immediate treat-
ment effect and the treatment effect on the trend. Because
variance estimates are expected to be positively skewed, due
to truncation of negative estimates to zero, we calculated the
median (relative) deviation of the estimates from the popu-
lation value, rather than the mean (relative) deviation, to
evaluate the (relative) bias in the estimates. We discuss only
the between-case variance and the between-study variance
of the immediate treatment effect (σ2u2 and σ

2
v2
), because

similar results are obtained for the treatment effect on the
time trend (σ2u3 and σ

2
v3
). The bias of the estimated between-

study variance and the estimated between-case variance of
the immediate effect is larger when there are only 10 studies
and 15 measurement occasions involved. The conditions
with the largest relative bias all had 15 measurements, 4
participants, and a small between-study variance (σ2v2 0 0.5)

in common. If the effect sizes are corrected and we estimate
the between-study variance of the immediate treatment ef-
fect, we find relative parameter bias values across conditions
ranging from 17 % to 55 %, while the relative bias goes up
to a value of 313 % when the effect sizes are uncorrected.
Similar results are found for bσ2u2, where the relative bias in a
condition is maximum 119 % for the corrected effect sizes
and 326 % for the uncorrected effect sizes (see Table 5).
Overall, the adjusted model results in less biased variance
estimates.

External event fades away gradually over four subsequent
measurement occasions

Overall treatment effect

Bias The bias of bg200 for uncorrected and corrected effect
sizes is, respectively, −0.0073, t(51199) 0 −418, p < .001,
and 0.00057, t(51199) 0 38, p 0 .74. This means that there is
a significant negative bias for the uncorrected effect sizes,
whereas this is not the case for the corrected effect sizes, and
the models differ significantly, F(1, 102398) 0 0.009, p 0
.77. The bias for bg300, depends largely on the model type, F
(1, 102398) 0 30,476.1, p < .0001. The bias for the uncor-
rected effect sizes is significant (−0.19), t(51199) 0 −246.23,
p < .0001, whereas this is not the case for the corrected T

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554 Behav Res (2013) 45:547–559

effect sizes (0.000179), t(51199) 0 0.24, p 0 .81. For both
bg200 and bg300, the difference is largest when there are a small
number of measurements (I 0 15) involved.

MSE For both estimated treatment effects, the MSEs are
larger for the uncorrected effect sizes, in comparison
with the corrected effect sizes (see Table 6). For both
bg200 and bg300, the model type has a significant influence
on the MSE, F(1, 102398) 0 724.69, p ≤ .0001 forbg200,
and for bg300, F(1, 102398) 0 5,431.15, p < .0001. For both
estimated treatment effects, the MSE is large when the studies
are heterogeneous (σ2v2 0 2) and a small number of measure-

ment occasions (I 0 15) and studies (K 0 10) are used. The
difference between the models is largest when a small number
of measurements is used.

Estimates of the standard errors The difference between the
average relative bias in the standard errors of the uncorrect-
ed effect sizes equals 0.02 for both uncorrected and cor-
rected effect sizes when g200 is estimated.

Similar to the constant external event effect results,
the difference between the average relative bias in the
standard errors of the uncorrected effect sizes (M 0
39.3) and corrected effect sizes (0.06) for bg300 is larger
and statistically significant, F(1, 254) 0 129.66, p 0
.0001 (see Table 7). The difference in results due to
the model type is more obvious if there are a small
number of studies involved (K 0 10).

Coverage proportion Similar to the CP for the constant
external event effect, the mean CP for the uncorrected and
corrected effect sizes for the estimate of the immediate
treatment effect differ significantly at the 5 % significance
level for both bg200, F(1, 254) 0 3.92, p 0 .05, and bg300, F(1,

254) 0 3.25, p 0 .007. The CP with values smaller than .93
all have 15 measurement occasions, have a large between-
study variance (σ2v3 0 2.0), and occur when the effect sizes

are uncorrected (for both bg200 and bg300 ). Similar to the
constant external event effect, the CP is overestimated for
bg300 and when the effect sizes are uncorrected in the condi-
tion where 30 measurement occasions are included. In the
condition where I 0 15 and σ2v3 0 2.0, the difference between

corrected and uncorrected effect sizes is largest.

Variance components

The results are similar to the results of the constant external
event effect, and results are less biased using the adjusted

Table 6 MSE of bg200 and bg300 in the g200 0 2, g300 0 0.2, and σ2u2 0 0.5 conditions for the external event effect fading away gradually over four
subsequent measurement occasions

bg200 bg300
Corrected Uncorrected Corrected Uncorrected

K J σ2v2 I 0 15 I 0 30 I 0 15 I 0 30 I 0 15 I 0 30 I 0 15 I 0 30

10 4 0.5 0.14 0.11 0.34 0.12 0.09 0.01 0.12 0.01

2 0.31 0.24 0.47 0.27 0.13 0.03 0.14 0.03

7 0.5 0.09 0.06 0.18 0.09 0.01 0.01 0.10 0.01

2 0.22 0.23 0.32 0.22 0.03 0.02 0.12 0.02

30 4 0.5 0.05 0.03 0.11 0.04 0.04 0.004 0.11 0.01

2 0.11 0.09 0.17 0.09 0.04 0.01 0.12 0.01

7 0.5 0.03 0.02 0.06 0.02 0.004 0.002 0.09 0.01

2 0.08 0.08 0.10 0.07 0.01 0.01 0.1 0.01

“Corrected” and “uncorrected” refer, respectively, to corrected effect size and uncorrected effect size for external event effects

Table 7 Difference between the median of the standard error estimates
and the standard deviation of bg300 in the g200 0 2, g300 0 0.2, and
σ2u3 0 0.05 conditions for the external event effect fading away
gradually over four subsequent measurement occasions

Corrected Uncorrected

K J σ2v3 I 0 15 I 0 30 I 0 15 I 0 30

10 4 0.05 0.010 0.037 0.076 0.103

0.2 −0.031 −0.002 0.029 0.050

7 0.05 0.004 0.035 0.069 0.068

0.2 −0.001 −0.007 0.010 0.012

30 4 0.05 −0.018 0.022 0.039 0.061

0.2 −0.009 0.0003 0.022 0.024

7 0.05 0.002 0.021 0.038 0.040

0.2 −0.002 0.001 0.004 0.003

“Corrected” and “uncorrected” refer, respectively, to corrected effect
size and uncorrected effect size for external event effects

Behav Res (2013) 45:547–559 555

model. We only discuss the estimated variances for the
immediate treatment effect, because the results are similar
for the estimated treatment effect on the trend. When we
estimate the between-study variance and the effect sizes are
uncorrected, the bias ranges from −0.002 to 3.41, while it
ranges from 0.002 to 0.73 for the corrected effect sizes. So
the estimated variances depend on the model type, F(1,
102398) 0 1,631, p < .0001. Similar results are obtained
for the estimate of the between-case variance. The maximum
bias for the corrected effect sizes is 1.60, while it is 3.21 for the
uncorrected effect sizes, and these estimates depend on the
model type, F(1, 102398) 0 5,628.62, p < .0001.

Empirical illustration

In this section, we give empirical illustrations of the com-
parison of the modified three-level model in which external
events are taken into account with the uncorrected model.
Therefore, we used a part of the meta-analytic data set of
Heyvaert, Saenen, Maes, and Onghena (2012) in which
restraint interventions for challenging behavior among per-
sons with intellectual disabilities was investigated. We give
two empirical illustrations of the consequences of ignoring
the external event effect in a multiple-baseline across-
participants design. We illustrate first the consequences of
ignoring external events in a single study, and next the
consequences of ignoring external events in a three-level
meta-analysis.

Ignoring external events in a single study

To illustrate the regression analysis of a multiple-baseline
across-3-participants design, we use the study of Thompson,
Iwata, Conners, and Roscoe (1999), which was included in the
meta-analysis of Heyvaert et al. (2012). In their study, the
effects of benign punishment on the self-injurious behavior of
individuals who had been diagnosed with mental retardation
was investigated. The 3 participants were measured repeatedly
over time on 22 measurement occasions, and the intervention
started on sessions 11, 13, and 20, respectively (see Fig. 2).
From this figure, we might expect that there is an immediate
reduction in challenging behavior when the treatment is intro-
duced and that the effect of the treatment on the challenging
behavior decreases over time (so there is a positive effect on
the time trend during the treatment). We also see that the 3
participants’ scores on measurement occasions 4 and 10 are
possibly influenced by an external event.

Results

If we ignore possible external events in the regression analysis
before combining the effect sizes in the two-level meta-

analyses, the average immediate treatment effect over cases
for that study equals −25.58, and the average treatment effect
on the time trend over cases from that study equals −2.58. If
we take the external event into account by correcting the effect
sizes before combining them, the immediate treatment effect
equals −23.23, and the treatment effect on the time trend is
1.24. This means that bg200 is 9.19 % smaller when the effect
sizes are corrected, in comparison with the uncorrected effect
sizes. Moreover bg300 is positive for the corrected effect sizes,
whereas it is negative for the uncorrected, which means that
the effect of the treatment over time decreases for the corrected
effect sizes, whereas it increases for the uncorrected.

Ignoring external events in a three-level meta-analysis

The three-level analysis of SSED data includes summarizing
the immediate treatment effect and the treatment effect on
the time trend over participants and over studies.

We estimate the immediate treatment effect and the treat-
ment effect on the time trend across seven studies. Again,
we use the meta-analysis of Heyvaert et al. (2012) to ran-
domly select multiple-baseline across-participants studies.
We combined the multiple-baseline across-participants

Fig. 2 Graphical display of a multiple-baseline design across-3-
participants designs using data from the study of Thompson, Iwata,
Conners, and Roscoe (1999)

556 Behav Res (2013) 45:547–559

study of Lindberg, Iwata, and Kahng (1999), Chung and
Cannella-Malone (2010), Zhou, Goff, and Iwata (2000),
Thompson et al., (1999), Hanley, Iwata, Thompson, and
Lindberg (2000), Rolider, Williams, Cummings, and Van
Houten (1991), and Roscoe, Iwata, and Goh (1998). In all
these studies, the same dependent variable was measured—
namely, the reduction in self-injurious behavior. Again, we
compare the three-level meta-analysis of uncorrected and
corrected effect sizes.

Results

With the uncorrected effect sizes in the three-level meta-
analysis, the overall immediate treatment effect equals −33.14,
t(6.39) 0 −3.44, p 0 .012, and the overall treatment effect on the
time trend equals −4.42, t(3.95) 0 −1.52, p 0 .19. When the
effect sizes are corrected before estimating the effects over
participants, the immediate treatment effect equals
−21.07, t(6.88) 0 −1.13, p 0 .30, and the treatment
effect on the time trend equals −0.43, t(1) 0 −0.28,
p 0 .83. This means that the immediate treatment effect
of the corrected effect sizes is 36.42 % smaller, as
compared with the uncorrected effect size, and the treat-
ment effect on the time trend for the corrected effect
size during the treatment is 90.27 % smaller.

This is consistent with the results of the simulation study,
where we found that the estimated treatment effects are
biased when the effect sizes are uncorrected before combin-
ing them in the three-level meta-analysis.

Discussion

External event effects are common in SSEDs because
single-case researchers often implement these kinds of
designs in everyday scenarios where they cannot control
for outside factors (Christ, 2007; Kratochwill et al., 2010;
Shadish et al., 2002). External events are not always antic-
ipated by researchers, and thus, they may not be measured
during the conduct of the study. Furthermore, the size of an
event effect may be small, and researchers may be unaware
of it even after the study has been completed. Whether
researchers recognize an external event or not, the failure
to account for the event in a meta-analysis can bias the
estimate of the treatment effect. Thus, we searched for a
method with which to model external events that could be
applied even when the events had not been previously
identified. Because we used a multiple-baseline across-
participants design, there was a need to take into account
the interdependence of the participants. Therefore, an exter-
nal event that influenced the scores of 1 participant was
assumed to influence the scores of the other participants in
the same study.

We discussed two possible scenarios. In one scenario, the
external event effect remains constant and influences the
scores of all participants within a study on four subsequent
moments. This occurs, for example, when a teacher is ill and
a substitute teacher takes over the classroom or when a
foreign observer is present on subsequent measurement
occasions. In the second scenario, the external event’s effect
would likely gradually fade away over four subsequent
moments. For instance, the influence of a teacher intern on
the behavior of students reduces over time. Moreover, the
model adjusted for external event effects takes into account
that measurement occasions closer in time are more related
than measurement occasions further in time.

We evaluated this approach using a large simulation
study and gave some empirical examples. If there is an
external event effect of zero, both models (the one that
corrects for moment effects and the one that does not)
are appropriate. If the external event influences subse-
quent scores for all the participants within a study, the
three-level approach for uncorrected effect sizes is not
recommended, because the estimates of both treatment
effects (i.e., immediate effect on level and effect on
time trend) are substantially biased. The MSE, standard
error, and CP are better estimated when the modified
model, which includes moment effects, is used. The
difference between the corrected and uncorrected effect
sizes is largest when there are a small number of studies
and measurement occasions, so in this context, we
advise using the adjusted model. Moreover, the adjusted
model results in less biased variance estimates.

But, of course, we should be aware of some limita-
tions. We assumed that all the participants within a
study are influenced the same way by the external event
effect. It is possible that different participants from the
same study are at separate locations and, therefore, are
not all influenced by the external event. Modeling event
effects that are not common to all participants in a
study is an important avenue for future research. We
chose to keep the number of measurements within a
study constant for all participants within the same study.
Of course, it is possible that different participants of the
same study have different series lengths. Furthermore,
we cannot generalize these results to other conditions
not involved in this simulation study, but we partially
addressed this by simulating a large number of condi-
tions and choosing realistic values for the parameters.

Another limitation is that we assumed linear trajecto-
ries in the treatment phase, which might not be true in
some real situations. To simplify the simulation model,
we further did not account for a possible dependence
between regression coefficients, which can be accounted
for in a multilevel analysis by estimating the covariance
at the various levels.

Behav Res (2013) 45:547–559 557

In addition, subjects in MBDs are repeatedly measured,
and succeeding measurements may be more related to each
other than measurements further away in time. We did not
account for this possible autocorrelation and suggest that
this as a useful extension to the present study.

Kazdin (2010) argued that there needs to be a minimum
of three measurement occasions between the participants in
an MBD in order to show an experimental effect. We did not
take this into account in the condition where the number of
measurement occasions was 15, because it was not possible
to do this and provide each of 7 participants a unique
baseline. We could alter the intervention schedule to intro-
duce the treatment for some participants (e.g., randomly
selected pairs) at the same moment. Examining this strategy
specifically and alternative intervention schedules more
generally would allow further research to extend results to
a wider range of multiple-baseline applications.

It can be difficult to attribute simultaneously unusual
outcome scores for all participants within a study to an
external event effect. If there is no external event effect,
we can still use the corrected model, because both the
corrected and uncorrected effect sizes will be unbiased
and, thus, there is no need to identify before the analyses
whether an external event effect occurred or not. We advise
single-case researchers to first use both models in the sen-
sitivity analysis and then decide which model to use. If
researchers are interested in the occurrence of external event
effects, we recommend that they keep a log in order to
identify potential outside factors that may influence the
scores at certain measurement occasions and include dum-
my indicator variables at least for these moments.

The extension of the three-level model for multiple-
baseline across-participants designs to include modeling of
potential external effects makes it even more appropriate
and useful for the analysis of realistic SSED data sets. This
study has indicated that the three-level model corrected for
external event effects provides better results than does the
uncorrected model for combining results from multiple-
baseline across-participants data, especially if there is only
a small number of observations (I 0 15) and a small number
of studies (K 0 10) in the synthesis. As was found here, even
when an external event effect is small, a failure to correct for
it can lead to biased effect sizes. Thus, applied SSED
researchers are encouraged to consider use of the three-
level model that corrects for external event effects when
synthesizing results of MBD data.

Author Note Mariola Moeyaert, Faculty of Psychology and Educa-
tional Sciences, University of Leuven, Belgium; Maaike Ugille, Faculty
of Psychology and Educational Sciences, University of Leuven, Belgium;
John M. Ferron, Department of Educational Measurement and Research,
University of South Florida. S. Natasha Beretvas, Department of Educa-
tional Psychology, University of Texas; Wim Van den Noortgate, Faculty

of Psychology and Educational Sciences, ITEC-IBBT Kortrijk, University
of Leuven, Belgium.

This research is funded by the Institute of Education Sciences, U.S.
Department of Education, Grant R305D110024. The opinions
expressed are those of the authors and do not represent views of the
Institute or the U.S. Department of Education.

For the simulations, we used the infrastructure of the Flemish
Supercomputer Center, financed by the Department of Economy,
Science and Innovation–Flemish Government and the Hercules
Foundation.

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Behav Res (2013) 45:547–559 559

  • Modeling external events in the three-level analysis of multiple-baseline across-participants designs: A simulation study
    • Abstract
    • Three-level meta-analysis
    • Correcting effect sizes for external events
    • A simulation study
      • Simulating three-level data
      • Varying parameters
      • Analysis
    • Results of the simulation study
      • Constant external event over four subsequent measurement occasions
        • Overall treatment effect
        • Variance components
      • External event fades away gradually over four subsequent measurement occasions
        • Overall treatment effect
        • Variance components
    • Empirical illustration
      • Ignoring external events in a single study
        • Results
      • Ignoring external events in a three-level meta-analysis
        • Results
    • Discussion
    • References
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