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1999, Vol. 23, pp. 809422
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1
THE VIDEO-RECORDED STROOP COLOR-WORD NEW MODEL OF EXPERIMENTALLY-INDUCED JOSE ROBERTO LEITE’ VANIA A. SARTORli
Science
All rights reserved
TEST AS A ANXIETY
MARIA DE LOURDES V. SEABRA’, and ROBERTO ANDREATINI’
’ Departamento
de Psicobiologia, Universidade Federal de Sao Paulo Escola Paulista de Medicina, S%o Paulo, SP, Brazil 2 Laboratorio de Fisiologia e Farmacologia do Sistema Nervoso Central, Departamento Farmacologia, Universidade Federal do Parana, Curitiba, Parana, Brazil (Final form, June 1999)
de
Abstract Leite, The video-recorded
de Lourdes V. Stroop Color-Word Test as
A. Sartori and Roberto new model of PP. 809-822.01999
El=er
scienceInc.
The of the Stroop Color-Word as a model of was evaluated. 2. the authors examined the influence of and the of instructions on anxiety state level. 50 State-Trait Anxiety Scale in anxiety state (2 minutes) and error was blocked by 5.0 p.o. on pre- and post-test measures, but was not changed by placebo administration. 3. public performance simulation was effective to the anxiety state on 30 and 50 on STAI). was prevented 5.0 p.o. but was not prevented with placebo administration. 4. a whole, these the Video-recorded Stroop Color-Word Test is an effective anxiety provoking to detect the effect of standard anxiolytic and stressed the importance of trait anxiety level the instructions on
of variance
(ANOVA),
diazepam
810
J.R. Leiteet al. Introduction
The best procedure the double-blind
for confirmation
randomized
long lasting, involving
clinical trials with anxious
presents
some problems,
among many others that constitute drug effects in terms of anxiety of anxiolytic
the clinical improvement
experiments
effect in clinical compounds elicit
setting.
evaluation
relevant
advantages
indicated
symptoms,
compounds
on normal
drugs (experimentally
by following
and Fisher,
1978). These
to clinical trials: (1) the volunteers
control and homogeneity drug side-effects
test, Stroop
color-word
experimentally-
other authors
et al., 1988).
color
for the initial
methods).
(Stroop,
urinary adrenaline,
that
screening
The induction
ways: (a) laboratory
procedures,
laboratory
procedures
have some
of e.g.
relative
will be recruited easily; (2) rapid execution;
of induced anxiety;
(4) more “pure” anxiety
test, etc.) and simulated
public speaking
(3)
symptoms;
(5)
arithmetical
are the most frequently
Test (SCWT) consists
of submitting
1935). The SCWT induced
heart rate, respiration
the subjects
effect was proposed
physiological
rate, electrodermal
(increase
activity,
in plasma
by Nakano et al. (1978a;
in higher trait-anxiety
in the state anxiety (Cibopogon
volunteers).
level induced
citratus
effect with lorazepam
staph).
(improvement
and
situation
anxiolytic
1978b), but in theirs studies they focused
of state-anxiety
a
etc.) and psychological
changes that can lead to suppose that it is a stress-inducing
as an indirect measure
reduced anxiety
to a cognitive
a color of a colorful word that denotes
et al., 1988; Tulen et al. 1989). The use of the SCWT to evaluate
lemongrass
anxiolytic
procedure
e.g. dental surgery; (c) drug administration,
in which they have to nominate
(distress and anxiety)
performance
anxiolytic
these putative
profile (McNair et al., 1982). Mental test task (mental
Color-Word
condition
(Kilminster
have
induced methods used.
The Stroop conflicting
anxiety
have related
have potentially
volunteers
induced
(b) real life situations,
clearer
is a symptom
Thus, it is difficult to explain
effects (Liebowitz
that many
symptoms
level can be elicited
(Pillard
is
Besides this,
while some authors
depression
with direct anxiolytic
greater
anxiolytic
the core of anxiety disorders.
Thus, how do we make a choice among
public speaking;
e.g. caffeine
(change
such procedure
reduction only (Debus and Janke, 1980). This can be seen in
anxiety
of anxiolytic
higher state-anxiety
different
However,
to test in clinical trials? A rational way is the use of a laboratory
clinically
simulated
patients.
such as the fact that anxiety
with reduced secondary
have
drug effect from animal data is
and thus it is expensive.
effect of tricyclic antidepressant:
related the clinical improvement Animal
anxiolytic
many patients and researchers,
the study with patients
the evaluation
of predicted
performance
drug on
related with
Leite et al. (1986), using a direct approach
by SCWT), did not find anxiolytic
More recently,
Tulen et al. (1991)
effect of the did not detect
using the SCWT and Palma et al. (1994) found that
the
Experimentally induced anxiety by the Stroop Test
SCWT did not cause a significant In the study of anxiolytic variable.
Despite
influence
of this personal
anxiety
situations
increase in anxiety level.
drug effects in normal volunteers,
the control
of the mean
attribute
is not clear.
trait anxiety
in the response
Moreover,
Thus the contradictory
the trait anxiety
among
is an important
experimental
of the subject
may be due to the different results described
above
groups,
the
to experimental-induced
other factor that can contribute
results of the SCWT with benzodiazepines by the subjects.
811
to contradictory
instructions
received
could be due to these two
factors The aim of the present experiementally-induced trait-anxiety anxiety
study
anxiety.
was to verify
Thus, it was investigated
and the video-recorded
of the subjects
submitted
procedure
(DZP), relative
to placebo
of the SW/T the influence
(public performance
to SCWT. Moreover,
drug effect must be sensible to antianxiety diazepam
the utility
as a model
of instructions,
simulation)
of the
in the state-
since a valid test to study anxiolytic
effects of establishing
(PLA), on state anxiety
clinical drugs, the effect of
of subjects submitted
to SCWT
was evaluated.
Methods Subiects Ninety-two
healthy
volunteers
(39 male and 53 female,
with age ranged
years) in good physical healthy, without history of past or current psychiatric or drug abuse and not using any prescribed color-blind.
Each volunteer
medication
into three groups according
the State-Trait
Score (Spielberg
median trait group (between protocol
was approved
accordance
with
by
disorder,
were the subjects.
to their scores obtained
alcohol
No subject was
prior to entering the study gave a written informed
subjects were allocated Anxiety
from 18 to 45
consent.
The
in trait portion of
et al, 1970): high trait group (equal or above
50),
31 and 49); and low trait group (equal or below 30). The study the ethic committee
the 1964 Declaration
of Escola Paulista
of Helsinki and
de Medicina
Brazilian ethic guidelines
and it is in of National
Health Council. Druas Diazepam, gelatinous
5.0 mg (Roche,
Brazil)
capsule, on a double-blind
and glucose
schedule,
were
administered
120 minutes before the test.
orally
in identical
J.R. Leite et al.
812
Anxiety Measure The State Trait Anxiety
Inventory
(STAI) consists of two separated
self-report
scales with
20 items each (scores ranging from 20 to 80). The two scales assess respectively (transitory)
and trait (personality
was translated
and validated
The Stroop Color-Word In the Stroop color-word
characteristic)
to Portuguese
(Spielberg
(Biaggio and Natalicio,
et al., 1970).
It
1979).
Test
Color-Word
Test (SCWT)
card. The word card had
three basic cards were used: word, color and
five color names (red, green, yellow,
printed in black letters on white background name appearing
levels of anxiety
population
the state
and set randomically
blue and violet)
in a 10x10 matrix,
20 times, but with the caution that each color appears twice
each
in each row and
did not occur next to itself in any line. These criteria were also used to construct the color and color-name
cards. The color card was made with each color printed with its corresponding
color (e.g. the word red printed printed in an incongruous
in red ink). The color-word
card consisted
of color names
color (e.g. the word red printed in yellow ink). The task was to read
aloud the color names (card word) or color ink (cards color and color-word). Procedure Experiment tested
I- Ten subjects
in two different
of each trait anxiety
sessions,
need for both speed and accuracy in the execution was evaluated
level group (high, median
1 month apart. In Session
before the instructions
(baseline)
I the instructions
and after the SCWT (post-test)
but added with the advice that the task in the third card (color-word) and any error was signalized
considered
were: loss of sequence
stressed
the
of the 3 cards of the SCWT. State-anxiety
portion of the STAI. In Session II the subject received the same instructions
minutes
or low) were
by a sound
of colors, repetition
of a ringing
by the state
described
above
should be done within 2 bell. The types
of error
of colors, mixed up of colors by words
and each color that was not read aloud because the time finished. Experiment
II- The test procedure
is the same of the Session II of the Experiment
with limited time and error signal on color-word
card). The state-anxiety
state portion of STAI before drug administration SCWT (post-drug), Experiment submitted
(baseline),
was evaluated
I (SCWT by the
after drug intake and before the
and after the SCWT (post-test).
Ill- Two groups with 18 volunteers
to the color-word
the second group received
in each were tested. In the first group was
card of the SCWT with limited time (2 minutes) and error signal; the same task but the test execution
was recorded
by a video-
Experimentally induced anxiety by the Stroop Test
camera and
and the image was simultaneously
the experimenter.
posterior
analysis
before
(basal),
It was told to the volunteer
of his(her)
Stroop Color-Word
projected
performance.
monitor to the volunteer
that the videotape
This later situation
Test (VRSCWT). State-anxiety
after reading
in a television
813
be used to
was called Video-Recorded
was evaluated
fifty colors, which correspond
would
by the state portion of STAI
to half of the color-word
card
(during), and at the end of the SCWT (post- test). Experiment
IV- Sixteen subjects were randomly assigned to one of two groups (placebo
diazepam
- 5 mg p.o.) under double-blind
submitted
to the VRSCWT.
State-anxiety
the same moment of the Experiment
condition.
Two hours later, the subjects
state was evaluated
or
were
by the state portion of STAI at
III (basal, during and post-test).
Data Analysis The statistical groups
was evaluated
Friedman
was performed by
ANOVA followed
Differences other
analysis
in baseline
with non-parametric
Mann-Whitney by Wilcoxon
U test, while
matched-pairs
scores in each experiment
methods.
within
signed-rank
were evaluated
Difference
effect
was
between
evaluated
by
test when appropriated. by the raw data. At the
phases, the delta phase value (phase score minus baseline) was used.
Results Experiment
I
Figure 1 presents the results of the two types of instructions anxiety
levels, In Session
Session
II (with
increase
in state-anxiety
from baseline to post-session
showed
group. In
a significant
(T= 0.00; p c .02), while subjects with
only showed a trend to increase (T= 5.5; .I0 > p > .05) and the low trait
group had no change (T= 14.5; p > .lO). Besides this, the delta value (post- session
score minus baseline .05), with anxiety
at any trait- anxiety
limited time and error signal) the high trait subjects
median trait anxiety anxiety
I there is no change in state-anxiety
of the SCWT in different trait-
score) differed significantly
the high trait-anxiety
among the three groups (H2,30= 6.14;
group with higher state-anxiety
group (U= 17.0; p < .05), and the median trait anxiety
(difference
not significant
relative
Session II was only significant
to other groups).
in high trait-anxiety
p <
score relative to the low traitgroup in intermediate
The delta value between
group (T= 8.50; p < .05).
position
Session
I and
J.R. Leite et al.
814
WITH ERROR SIGNAL
ERROR SIGNAL AND TIME LIMIT
WITHOUT
AND TIME LIMIT *
50 r
LOW
MEDIAN
HIGH
LOW
MEDIAN
HIGH
TRAIT ANXIElY 10 BASELINE
I
POST-TEST]
Fig 1. Effect of instructions of Stroop Color Word Test (SCWT) and trait-anxiety level on stateanxiety score (STAI) of normal volunteers (10 per group). Left side: SCWT without limited time and error signal; right side: SCWT with limited time and error signal. Data represents mean + S.E.M. * significantly different from baseline
* q PlA
+ DZP
45
40
35
30 L
BASELINE
POST-DRUG
POST-TEST
Fig 2. Effect of diazepam (DZP), 5.0 mg p.o., or placebo (PLA) on state-anxiety score (STAI) of subjects with high trait-anxiety level submitted to SCWT with limited time and error signal (10 per group). Data represents mean + S.E.M. l significantly different from baseline in DZP group + significantly different from post-drug PLA group # significantly different from pre-drug in PLA group
Experimentally induced anxiety by the Stroop Test
Experiment Figure
II
2 shows
submitted
815
the effect of diazepam
to the SW/T
in state-
anxiety
of high trait-anxiety
with limited time and error signal. There is a significant
after DZP ( xzr= 10.34; p < .Ol) and a significant
state-anxiety
p c .002). In DZP session there is a decrease
in state-anxiety
subjects
reduction
in
increase after PL4 (xzr= 12.67; in post-drug and post-test score
(T=O.OO; p < .Ol and T= 1.50; p < .02, respectively).
The PLA session
showed an increase
in state-anxiety
(T= 0.00; p < .Ol)
and a trend relative
to baseline
relative
between
to baseline
score in post-test relative to post-drug
(T= 8.00; .I0 > p > .05). There was a significant
difference
PLA and DZP post-test score (T=O.OO; p c .Ol).
I A
*
scwr
-+vRSCwr
3oT
BASELINE
DURING
POST-TEST
Fig 3. Effect of video-recorder of SCWT with limited time and error signal (VRSCWT) on stateanxiety score (STAI) of subjects with median trait-anxiety level. SCWT with limited time and error signal without video-recorder was used as control procedure (16 per group). Data represents mean f S.E.M. * significantly different from baseline and post-test in VRSCWT.
Experiment
Ill
The Fig 3 shows the influence anxiety
of median-trait
is an increase increase
anxiety
subjects.
in state anxiety
In the group
across the session
during the SCWT relative to baseline
7.50, p < 0.02, respectively). anxiety
of video-recorder
with video-recorder
exhibition
on state-
of the SW/T
there
(xzr= 13.09, p < 0.02), with a significant
and post-session
(T= 1.00, p < 0.002 and T=
In the group without video- recorder there is no change in state-
(xzr= 3.80). The difference
the SCWT (U= 117, p < 0.03).
with simultaneous
between
groups was significant
only in delta value during
J.R. kite
816
Experiment
et al.
IV
The effects of diazepam
or placebo
time, error signal and video-recorder increase
in state-anxiety
increase
in anxiety
in state- anxiety (VRSCWT)
scores across the SCWT with limited
are shown
in Fig 4 (STAI). There
score (x*r= 10.75, p < 0.001) in the placebo
score during the SCWT and in the post-session
(T= 1.00, p < 0.02 and T= 2.50, p < 0.03, respectively).
group. There
in contrast
to
is an is an
baseline
In DZP group there is no change on
STAI scores across the SCWT (x*r= 1.35).
* I
PL4
+ DZP
I
I
1
DURING
BASELINE
I
POST-TEST
Fig 4. Effect of diazepam (DZP), 5.0 mg p.o., or placebo (PLA) on state-anxiety score (STAI) of subjects with median trait-anxiety level submitted to the Video-Recorder Stroop Color Word Test (VRSCWT). Data represents mean f S.E.M. * significantly different from baseline in PLA group.
Discussion The results of the present study show that experimental change
the state-anxiety
response
also seems that the procedure and video-record)
is a suitable
of normal volunteers
used in Experiment model
procedures
and personal
attributes
to the Stroop Color- Word Test. It
IV (SCWT with limited time, error signal
for experimentally
induced
anxiety
in subjects
with
median trait anxiety. The Role of Trait Anxiety and Instructions In the Experiment submitted
I there was no change in state-anxiety
to the “traditional”
of any trait-anxiety
group when
form of the SCWT. which was similar of results of Palma et al.
Experimentally
(1994). However,
induced anxiety by the Stroop Test
when the level of difficulty of the task was increased
817
by limiting the time to
perform the task and the stress was increased by the signal of the errors committed, with high trait-anxiety
showed a significant
by DZP 5 mg (Experiment baseline (post-drug
measure).
volunteers”
(Brauzer
induction
to study
resemblance clinical
anxiolytic
patients,
use of such subjects The importance
through
The modifications
volunteers”
population
some
and their refuse to participate
in
the negative
with the
results
et al., 1995).
of experimentally-induced response
to the SCWT
results found in some studies
of Palma et al. study (Palma et al.,
in the instruction,
introduced
that
in our study stressed the need
in the SCWT here could have affected
and retention
the state-anxiety
in
made the task more stressful and difficult (Dyer, 1973) and
of the task difficult (Jensen
self- image, which may elicit increase in state-anxiety
and Rohwer,
1966), which could
as a threat to the self-concept
or
(Geller and Shaver, 1976; Boucsein and
1980).
Public Performance The introduction on TV screen,
Simulation of the video-cassette
commonly
al., 1982, Guimaraes
recorder
seen in procedures
is a common
proposed
to represent
However,
besides the speaking,
other situations
fear among
the student anxiety
the public performance
like as psychological
of image (McNair et
in median trait subjects
effect of SCWT with public performance
tests, e.g. memory test (Kohnen and Lienert,
a form of unconditioned
and Savage,
exhibition
public performance
et al., 1987), was able to increase state-anxiety
also seen with other psychological public speaking
and the simultaneous
that simulated
Ill). This increase in the anxiogenic
play (James
of
level on the anxiety
could explain
clinical
problems
advantages
induce more errors. The error signal could be interpreted
(Experiment
some
and to the error signal.
different ways. The time limitation
Wend&Suhl,
share
1988; Pieters et al., 1992; Gorenstein
of trait-anxiety
The discrepancy
of speed and accuracy,
there is no need of anxiety
and thus they have some of the practical
may be due to the differences
made learning
“Symptomatic
eliminated
this experiment
(Tulen et al _, 1991). 1994)
effect.
at only
who can be called “symptomatic
1973; McNair et al., 1980),
drug
had high state-anxiety
could be seen after drug administration
like their low rate in general
models.
suggests
and Goldstein,
which could be reduced
these subjects had already
already
(Glass et al., 1981; Antrobus,
the
anxiety
reduction
This suggests that with the subjects,
with anxious
studies,
experiments Thus,
II). However,
and a significant
increase in state-anxiety,
subjects
population reaction
(Geer,
(Deakin
also increases
was
1980).
The
1965) and it is
and Graeff,
1991).
the state anxiety
in
tests (e.g., Kohnen and Lienert, 1980; this study), music
1984) and physical
exercise
(Ferreira
and Murray,
1983). This
J.R. Leite et al.
818
suggests that the public performance the task performed.
is a potent anxiety eliciting procedure
This can be due to the increase
induced by public performance
of self-awareness
There are some requirements
Anxiety
induced;
that an experimentally-induced
of volunteers;
conditions.
It elicits
volunteers
increase in anxiety state; (b) facility
(c) the control the intensity and the quantification
anxiety
researchers
self-limited
more probably
(e) able to detect the effect of
increase
is
easily
aspect,
to perform
met these
state
in normal
since it was found that in pharmacological
refused to participate
anxiety that is detected
the VRSCWT
in anxiety
refused to participated
In this line, none volunteer
The method elicited a subjective Moreover,
and
trait. This is an important
with higher trait anxiety
studies (Antrobusl988).
of anxiety
drugs. The present study showed that the VRSCWT
a quantifiable
with median
subjects
limited.
anxiety have to meet (McNair
(d) it must be simple, easy and rapid to perform; clinical anxiolytic
and self-monitoring
Model
et al., 1982; Griez, 1984): (a) an induction of a reversible
established
of
(Geller and Shaver, 1976).
The VRSCWT as an Experimentallv-induced
in the recruitment
independently
in the VRSCWT.
by the scale used and that is selfand need
only
a small
team
of
to be carried..
The Stroop effect appears 1991). Furthermore, of prior knowledge
to be universal
and
the SCWT is a standardized or familiarity
VRSCVVT over the simulated
of the volunteer
is present in different test (Lezak,
cultures
(MacLeod,
1995), but with low probability
with the test. It may some advantage
public speaking (SPS), probably the most frequently
to
model used
to induced an increase in anxiety state. In the SPS the subject has to prepare a speech about a topic
selected
(Droppleman
at the
moment
of the
test
and
delivered
it before
camera
and McNair, 1971; Lipper and McNair, 1972; McNair et al., 1982). While in some
studies the topic to be selected
is related to a personal
experience
situation
et al., 1997) in others
the topic
of his life (Guimaraes
nonemotional
a video
subject like political or academic
like the most stressful is a non-personal
(McNair et al., 1982; Guimaraes
and
et al., 1987;
1989). Another state-anxiety
aspect that deserves
further consideration
is the sensibility
increase with VRSCWT was blocked by DZP administration.
that the effective
DZP dose used in this study
used in others experimentally
induced anxiety,
of the method.
It is worthy to note
was lower than the effective dose (10 - 20 mg) e.g. simulated
public speaking
(McNair et al.,
1982; Graeff et al., 1985; Guimaraes
et al., 1989). This may suggest a higher sensitivity
VRSCWT.
characteristic
This
is an
interesting
The
since
it can
reduce
the
of the
probability
of
819
Experimentally induced anxiety by the Stroop Test
appearance
of dose-related
Although
side effects in the evaluation
not measured
an objective
index
of new drugs with anxiolytic
in the present study, the performance
of sedation
and cognitive
impairments
Jones, 1987; Tulen et al, 1991), which may be an additional
effect.
in the SCWT can be used as
induced
by drugs (Hooker
advantage
of the VRSCWT.
and
Conclusion The results of the present study suggest that: (1) internal (trait-anxiety) pressure,
error signal and public performance
the state-anxiety Color-Word
response
to the Stroop
simulation)
Color-Word
and external
factors exerts an important
Test; (2) the Video-Recorded
Test is a useful and sensible method to study putative anxiolytic
(time role in Stroop
drugs.
Acknowledqements The authors Palacios supported
would
like to thank Dr. Jose Carlos F. Galduroz
for the assitance by Associacao
in receipt of a fellowship
on drug administration
Fundo de lncentivo
and Esther M. Nakamura-
and medical
a Psicofarmacologia
support.
This study
was
(AFIP). VAS and RA were
from FAPESP and CAPES respectively
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Inquiries and reprint request should be addressed Jose Roberto Leite Departamento de Psicobiologia Universidade Federal de S%o Paulo Escola Paulista de Medicina R. Botucatir, 862, lo andar Sao Paulo, SP, Brazil 04023-062 FAX: 0055-Oll5725092 e-mail:
[email protected]
et al.
function
to:
during
rest
and
mental
stress,