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Validity of four pain intensity rating scales

TLDR
The validity of 4 common pain intensity measures is supported, although the 0–10 Numerical Rating Scale and Visual Analogue Scale evidenced the most responsivity, while the NRS emerged as being both most responsive and able to detect sex differences in pain intensity.
Abstract
The Visual Analogue Scale (VAS), Numerical Rating Scale (NRS), Verbal Rating Scale (VRS), and the Faces Pain Scale-Revised (FPS-R) are among the most commonly used measures of pain intensity in clinical and research settings. Although evidence supports their validity as measures of pain intensity, few studies have compared them with respect to the critical validity criteria of responsivity, and no experiment has directly compared all 4 measures in the same study. The current study compared the relative validity of VAS, NRS, VRS, and FPS-R for detecting differences in painful stimulus intensity and differences between men and women in response to experimentally induced pain. One hundred twenty-seven subjects underwent four 20-second cold pressor trials with temperature order counterbalanced across 1°C, 3°C, 5°C, and 7°C and rated pain intensity using all 4 scales. Results showed statistically significant differences in pain intensity between temperatures for each scale, with lower temperatures resulting in higher pain intensity. The order of responsivity was as follows: NRS, VAS, VRS, and FPS-R. However, there were relatively small differences in the responsivity between scales. A statistically significant sex main effect was also found for the NRS, VRS, and FPS-R. The findings are consistent with previous studies supporting the validity of each scale. The most support emerged for the NRS as being both (1) most responsive and (2) able to detect sex differences in pain intensity. The results also provide support for the validity of the scales for use in Portuguese samples.

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Validity of four pain intensity rating scales
Maria Alexandra Ferreira-Valente
a,b,c,
, José Luís Pais-Ribeiro
a,c
, Mark P. Jensen
d
a
Faculdade de Psicologia e Ciências da Educação da Universidade do Porto, Porto, Portugal
b
Portuguese Foundation for Science and Technology, Lisbon, Portugal
c
Unidade de Investigação em Psicologia e Saúde (Psychology and Health Unit), Lisbon, Portugal
d
Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA, USA
Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.
article info
Article history:
Received 22 February 2011
Received in revised form 25 June 2011
Accepted 11 July 2011
Keywords:
Pain assessment
Validity
Numerical Rating Scale
Visual Analogue Scale
Faces Pain Scale
Verbal Rating Scale
abstract
The Visual Analogue Scale (VAS), Numerical Rating Scale (NRS), Verbal Rating Scale (VRS), and the Faces
Pain Scale-Revised (FPS-R) are among the most commonly used measures of pain intensity in clinical and
research settings. Although evidence supports their validity as measures of pain intensity, few studies
have compared them with respect to the critical validity criteria of responsivity, and no experiment
has directly compared all 4 measures in the same study. The current study compared the relative validity
of VAS, NRS, VRS, and FPS-R for detecting differences in painful stimulus intensity and differences
between men and women in response to experimentally induced pain. One hundred twenty-seven sub-
jects underwent four 20-second cold pressor trials with temperature order counterbalanced across 1°C,
3°C, 5°C, and 7°C and rated pain intensity using all 4 scales. Results showed statistically significant dif-
ferences in pain intensity between temperatures for each scale, with lower temperatures resulting in
higher pain intensity. The order of responsivity was as follows: NRS, VAS, VRS, and FPS-R. However, there
were relatively small differences in the responsivity between scales. A statistically significant sex main
effect was also found for the NRS, VRS, and FPS-R. The findings are consistent with previous studies sup-
porting the validity of each scale. The most support emerged for the NRS as being both (1) most respon-
sive and (2) able to detect sex differences in pain intensity. The results also provide support for the
validity of the scales for use in Portuguese samples.
Ó 2011 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
1. Introduction
The Visual Analogue Scale (VAS), Numerical Rating Scale (NRS),
Verbal Rating Scale (VRS), and Faces Pain Scale-Revised (FPS-R) are
among the most common measures of pain intensity used by
clinicians and researchers. Evidence supports the reliability and
validity of each of these measures across many populations
[10,26–28]. However, each measure has strengths and weaknesses.
For example, research indicates that VASs have more ratio scale
qualities than other pain intensity scales for groups of patients
(but not necessarily for individuals) [13,42,44,45], although some
authors note that VASs scales do not always have linear qualities
and are not always normally distributed [37,55]. Pain scales with
more response levels (eg, the VAS or 0–10 NRS relative to the 6-
point FPS-R or 4-point VRS) have the potential to be more sensitive
[6,9,55], although more response categories do not necessarily
translate to more responsivity [7,19,29]. Furthermore, research
findings suggest that no single measure is consistently more
responsive than any of the other measures [6,9–11,28,30,36],
although the responsivity of the VAS, NRS, VRS, and FPS-R has
yet to be directly compared in the same study. Also, the validity
of these scales has never been examined in a sample of individuals
from Portugal. Evaluations of common pain measures in samples
from different countries and cultures can help establish the
cross-cultural generalizability of validity findings.
Perhaps the most important validity criterion for a pain measure
is its ability to detect changes in pain with pain treatment or proce-
dures known to produce pain. One method for doing this would be to
use an experimental design in which the amount of stimulation is
highly controlled [14]. The cold-pressor test is an experimental
method for inducing pain that is thought to reflect many (but not
all) ofthecritical components of clinical pain [25], and its advantages
are discussed in the literature [14,22,40,53]. Moreover, an increase
in pain intensity as water temperature decreases is well docu-
mented, with small variations in water temperature resulting in sig-
nificant differences in pain intensity [22,53,54].
A number of studies have examined the influence of sex on pain
perceptions and pain response to experimental pain [14,40], with
0304-3959/$36.00 Ó 2011 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
doi:10.1016/j.pain.2011.07.005
Corresponding author. Address: Rua 25 de Abril, n° 5, Idanha Belas, Belas
2605-119, Portugal. Tel.: +351 969082988.
E-mail address: mafvalente@gmail.com (M.A. Ferreira-Valente).
PAIN
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152 (2011) 2399–2404
www.elsevier.com/locate/pain

normally menstruating women usually being more sensitive to
painful stimuli than men [34,36,51,54]. Laboratory pain experi-
ments that include both men and women provide an opportunity
to compare the ability of pain ratings to detect these well-estab-
lished sex differences.
The primary aim of the current study was to compare the relative
validity of VAS, NRS, VRS, and FPS-R for detecting differences in pain-
ful stimulation and for detecting sex effects in response to painful
stimulation. Based on previous research, we hypothesized that all
4 scales would be able to detect a sex effect and differences in pain
resulting from 4 temperatures (1°C, 3°C, 5°C, and 7°C). Given the lar-
ger number of response levels of the VAS and NRS, we also antici-
pated that these would evidence greater responsivity than the VRS
or FPS-R. Finally, this study also sought to evaluate the validity of
the pain intensity rating scales in a Portuguese sample.
2. Methods
2.1. Participants
Participants were 127 volunteer university students. Exclusion
criteria included: (1) being under 18 years of age; (2) reporting a his-
tory of any of the following diagnoses or medical problems: muscu-
loskeletal problems, cancer, heart disease, stroke, epilepsy, diabetes
or Raynaud syndrome; (3) having an open wound, cut, or fracture in
any of the upper limbs; (4) having a cognitive or physical disability
that could prevent participation; or (5) refusal to participate.
Of the 127 subjects who expressed an interest in participating in
the study, 112 were eligible and completed the entire experimental
procedures. Of the 112 completers, 3 subjects were excluded from
the analyses because they were unable to understand how to use
the VAS. Thus, complete data were available for 109 subjects, 56 of
whom were female (51.4%). The ages of the participants ranged from
18 to 40 years old (M = 22.27, SD = 3.92; Female: M = 21.24,
SD = 3.45; Male: M = 23.34, SD = 4.13). Most of the sample had their
permanent residence in an urban area (74.3%), and the remainder
(25.7%) lived in a rural area. Ninety-nine participants were under-
graduate college students (33.0%, 17.4%, 21.1%, 11.0%, and 8.3% in
their first, second, third, fourth, and fifth year, respectively). Ten
(9.2%) of the participants were in graduate school.
2.2. Material
The cold-pressor apparatus used consisted of 4 thermal insu-
lated containers with 18.1 L of capacity containing water chilled
to 4 different temperatures. The apparatus was capable of main-
taining water temperatures within ±0.5°C of the desired tempera-
tures throughout the experimental procedures. Each container
had 2 compartments separated by a metal filter, one of which held
water, ice, and a water pump, and the other (the immersion tank)
contained water alone with an armrest; the participants’ hands
therefore never came in direct contact with the ice. Four water
pumps (JAD, model SP-602, 200 L/h, Guangdong, China) made the
water flow continuously between the 2 compartments of each con-
tainer to prevent warm water pockets from forming near the partic-
ipants’ hands [53]. The temperature of the hand and water was
monitored and controlled by asking the participants to hold a mer-
cury thermometer in the palm of their hands and immersing a ther-
mometer in the water, respectively. One extra thermal insulated
container without divisions contained an armrest and tepid water.
2.3. Measures
Fig. 1 presents all the pain intensity rating scales used in this
study. The VAS [23] consists of a horizontal line 100 mm in length,
with the end points ‘‘No pain’’ and ‘‘Worst imaginable pain’’ placed
at each end of the line. Respondents are asked to make a mark on
the line that best represents the level of pain intensity that they are
experiencing. The NRS is an 11-point scale consisting of integers
from 0 through 10; 0 representing ‘‘No pain’’ and 10 representing
‘‘Worst imaginable pain.’’ Respondents select the single number
that best represents their pain intensity. Although validity studies
for the Portuguese versions of these measures have not been pub-
lished, to our knowledge, both the VAS and the NRS used in this
study have been previously used in research with Portuguese sam-
ples [1,16,17,48], and are recommended for use by the Portuguese
Ministry of Health (Normative Circular n° 9/DGCG of June 14,
2003). The VRS is a 5-point scale consisting of a list of phrases
(no pain, mild pain, moderate pain, intense pain, maximum pain)
that describe increasing levels of pain intensity. Respondents select
the single phrase that best characterizes their pain intensity. The
VRS used in this study is commonly used by Portuguese research-
ers (eg, [12]). The FPS-R [4,21] is a 6-point scale, with 6 different
faces that represent increasing levels of pain intensity. Respon-
dents are asked to select the one expression that best characterizes
his or her pain intensity, from the left-most face (‘‘No pain’’), to the
right-most face (‘‘Very much pain’’). Each illustration corresponds
to a numeric score (0, 2, 4, 6, 8, or 10). Research supports the valid-
ity of each of the pain measures used in this study as measures of
pain intensity [24,27,32,39,44,46,47]. Although the FPS-R was ini-
tially developed for use with children, researchers also use the
measure in samples of individuals with cognitive and communica-
tion impairment. The Portuguese (Portugal) translation of the FPS-
R was performed by Batalha [2] and is available online
(www.painsourcebook.ca).
2.4. Procedure
The cold-pressor procedures closely followed the guidelines for
this task described in the literature, and were adapted to fit the
study aims [40,52,53]. The study had Institutional Review Board
approval. The study procedures were described to all potential par-
ticipants and each was given a written consent form to read and
sign before any measures were administered. After signing the
consent form, participants completed a demographic and medical
history questionnaire in order to identify potential medical condi-
tions that would prevent participation. Participants who met any
of the exclusion criteria were then excluded from participation.
Fig. 1. The Numerical Rating Scale, Visual Analogue Scale, Faces Pain Scale
Revised, and Verbal Rating Scale; Faces Pain Scale Revised, copyright Ó2001,
International Association for the Study of Pain, reproduced with permission,
www.painsourcebook.ca.
2400 M.A. Ferreira-Valente et al. / PAIN
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152 (2011) 2399–2404

The nondominant hand temperature was measured in all par-
ticipants, followed by hand washing to the wrist. The nondominant
hand was then immersed to the wrist in the container with tepid
water (36°C±1°C) for 2 minutes, in order to reduce preexisting dif-
ferences in hand temperature [53]. Hand temperature was again
measured, and participants were instructed to immerse the hand
to the wrist in the first cold water container for 20 seconds. Partic-
ipants were also told they could take the hand from the cold water
at any moment if it felt too uncomfortable to continue. For each of
the 4 study conditions, only 3 participants took their hands out
of the water before the established tolerance time (20 seconds).
After the 20-second cold immersion, when we anticipated that
pain would be at its most intense, we administered paper-and-
pencil versions of the 4 pain measures (VAS, NRS, VRS, and FPS-
R). The measures were presented in a random order using a Latin
Square design. After a 3-minute break, the participants were asked
to immerse his or her hand into the tepid warm water again for
2 minutes, and hand temperature was again assessed. Participants
underwent 4 trials with 4 different water temperatures (1°C, 3°C,
5°C, and 7°C), in counterbalanced order, as proposed by Mitchell
and colleagues [40]. Each participant experienced each water tem-
perature only once, and provided ratings using each of the 4 scales
for each temperature; thus, each participant provided 16 ratings.
Participants were not given any information regarding the water
temperature in each container.
2.4.1. Data analysis
We first computed medians, means, and SDs for demographic
and study variables for descriptive purposes. We next computed
Pearson correlations between the VAS, NRS, FPS-R, and VRS, for
descriptive purposes. In order to compare the ability of VAS, NRS,
FPS-R, and VRS to detect differences in pain stimuli resulting from
4 different temperatures, as well as the hypothesized sex main ef-
fect on pain intensity ratings, we then performed 4 mixed-design
repeated-measures analyses of variance (ANOVAs), with the pain
intensity ratings as the dependent variables, and sex and temper-
ature as the independent variables. Prior to these analyses, we
evaluated test assumptions, namely normality and sphericity of
the variance–covariance matrix, by analysing skewness (Sk) and
kurtosis (Ku), with values of Sk and Ku lower than 1 indicating ab-
sence of severe violation of normality assumption and Mauchly
test, respectively [5,18]. If a violation of the assumption of spheric-
ity was found, we planned to use Huynh-Feldt epsilon to set the
degrees of freedom [8,38]. In the event that a significant tempera-
ture effect was found, we planned to perform between-tempera-
ture comparisons using post hoc Fisher’s least significant
difference tests. Effect sizes were estimated using
g
2
p
, and, along
with P values and F statistic magnitudes, were used to compare
the hypothesized differences in responsivity of the 4 pain mea-
sures, with larger
g
2
p
and F statistics, as well as smaller P values,
indicating greater sensitivity [10,11,24,49]. Finally, we performed
power analyses to determine the sample size required to obtain
significant effects for each of the 4 measures, both for the omnibus
ANOVA and for each planned temperature paired comparison. Al-
pha was set at 0.05 and power at 0.95 for these analyses. Statistical
analyses were computed using software PASW Statistics 18 (v. 18,
SPSS Inc. Chicago, IL, USA) and G
Power (v. 3.1) [15].
3. Results
Table 1 lists the descriptive statistics of the study variables, and
Table 2 presents the correlation coefficients between the pain mea-
sures. As can be seen, the pain scales showed strong to very strong
and statistically significant inter-scale correlations (rs ranging
from 0.79 to 0.96) for all 4 water temperatures.
Pain ratings, as measured by VAS, NRS, VRS, and FPS-R, showed
normal distributions for each of the 4 temperatures (Sk <1 and Ku
<1). However, for each measure, we noted a violation of the
assumption of sphericity [VAS: W = 0.70, X2 (5) = 38.28,
p < 0.001; NRS: W = 0.59, X2 (5) = 55.53, p < 0.001; VRS: W = 0.82,
X2 (5) = 20.54, p < 0.01; FPS-R: W = 0.81, X2 (5) = 21.74, p < 0.01].
We therefore used Huynh-Feldt epsilon to determine the degrees
of freedom in the analyses [8,38].
As hypothesized, there were statistically significant tempera-
ture main effects for each of the 4 scales used in the study [VAS:
F
Huynh-Feldt
(2.48, 265.24) = 85.74; p < 0.001,
g
2
p
= 0.45;
p
= 1; NRS:
F
Huynh-Feldt
(2.28, 243.64) = 93.49; p < 0.001,
g
2
p
= 0.47;
p
= 1; VRS:
F
Huynh-Feldt
(2.74, 287.48) = 76.36; p < 0.001,
g
2
p
= 0.42;
p
=1;
FPS-R: F
Huynh-Feldt
(2.70, 286.42) = 72.62; p < 0.001,
g
2
p
= 0.32;
p
= 1]. Moreover, all of the effect sizes associated with the temper-
ature main effects in the omnibus ANOVAs for each measure were
large. Effect sizes for the comparisons for each pair of temperature
differences ranged from medium (0.17) to large (0.59), consistent
with the differences between temperatures. These differences also
follow the same pattern for each scale (Table 3 and Fig. 2).
Statistically significant sex main effects emerged for the NRS
[F(1, 107) = 4.40; p < 0.05,
g
2
p
= 0.04;
p
= 0.55], VRS [F(1, 107) =
8.38; p < 0.01,
g
2
p
= 0.07;
p
= 0.82], and FPS-R [F(1, 107) = 14.13;
p < 0.001,
g
2
p
= 0.12;
p
= 0.96], and a nonsignificant trend emerged
for the main effect of gender on pain ratings on VAS
[F(1, 107) = 3.49; p = 0.07,
g
2
p
= 0.03;
p
= 0.46], with women report-
ing higher pain ratings in every experimental condition.
Post hoc Fisher’s least significant difference paired tempera-
tures comparisons for each pain scale found statistically significant
differences between all observations (p < 0.001). As would be ex-
pected, in every case, lower temperatures resulted in higher pain
intensity ratings for all 4 scales.
The NRS and VAS evidenced slightly higher effect sizes (0.47
and 0.44, respectively) and higher F statistics (93.49 and 85.74,
respectively) than VRS (0.42 effect size and F statistic of 76.36)
and FPS-R (0.32 effect size and F statistic of 72.62). Power analyses
based on these effect sizes indicated that the number of partici-
pants needed to be able to detect an overall difference between
temperatures, as tested by an ANOVA, would be 5, 5, 5, and 7 for
the NRS, VAS, VRS, and FPS-R, respectively. Power analyses to
Table 1
Means and SDs of the pain ratings for each temperature condition.
Overall
Mean (SD)
Male
Mean (SD)
Female
Mean (SD)
VAS
7°C 3.65 (2.35) 3.23 (2.29) 4.03 (2.36)
5°C 4.38 (2.23) 3.90 (2.10) 4.82 (2.28)
3°C 5.04 (2.24) 4.67 (2.31) 5.38 (2.14)
1°C 5.83 (2.17) 5.58 (2.24) 6.05 (2.12)
NRS
7°C 3.87 (2.39) 3.43 (2.38) 4.29 (2.33)
5°C 4.64 (2.21) 4.13 (2.17) 5.12 (2.15)
3°C 5.32 (2.15) 4.96 (2.24) 5.66 (2.01)
1°C 6.18 (2.21) 5.83 (2.29) 6.52 (2.10)
FPS-R
7°C 3.33 (2.51) 2.52 (2.30) 4.11 (2.48)
5°C 4.15 (2.32) 3.32 (2.19) 4.95 (2.21)
3°C 4.95 (2.55) 4.08 (2.60) 5.78 (2.23)
1°C 5.76 (2.46) 5.17 (2.46) 6.29 (2.35)
VRS
7°C 2.49 (0.93) 2.26 (0.88) 2.67 (0.93)
5°C 2.79 (0.86) 2.55 (0.82) 3.00 (0.85)
3°C 3.08 (0.83) 2.87 (0.81) 3.30 (0.79)
1°C 3.50 (0.80) 3.34 (0.85) 3.63 (0.71)
VAS, Visual Analogue Scale; NRS, Numerical Rating Scale; FPS-R, Faces Pain Scale-
Revised; VRS, Verbal Rating Scale.
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compute the number of participants needed to detect differences
between each pair of temperatures for each of the pain scales are
presented in Table 3, and range from 5 to 19. These are consistent
with the distance between temperatures, with larger distances
(and effect sizes) corresponding to fewer participants needed.
4. Discussion
The results of this study provide strong support for the validity
of all 4 scales studied for detecting changes in pain intensity in Por-
tuguese university students. All of the scales were able to detect
differences in pain resulting from 4 different temperatures, with
variations in temperature resulting in statistically significant dif-
ferences in pain intensity ratings, and lower temperatures result-
ing in higher pain ratings for each of the 4 scales studied. These
results are consistent with previous studies that support each
scale’s validity [9,10,24,33,44,45], and show that small variations
in water temperature result in significant differences in pain inten-
sity ratings [22,40,53,54].
As predicted, we found some differences in the relative respon-
sivity, with NRS being the most responsive, followed by VAS, VRS,
and FPS-R. This is consistent with previous studies demonstrating
the superiority of VAS and NRS responsiveness, due perhaps to the
larger number of response levels that these 2 scales provide
[6,9,41,50,55]. In our study, the NRS has shown to be slightly more
responsive than the VAS, as indicated by its larger effect size and F
statistic value. This is consistent with a group of studies showing a
similar sensitivity between the NRS and VAS or a slight superiority
of the NRS over the VAS [6,9–11]. Nevertheless, the results of
power analyses to determine the number of subjects needed to de-
tect a significant effect indicate that the 4 measures have very sim-
ilar levels of responsivity, with very small differences between
scales in the numbers of subjects needed to detect differences. This
finding is consistent with the strong to very strong associations we
found among the study measures (a finding also consistent with
previous research, eg, [11,24,33,46]), indicating that all 4 measures
tap into the same overall dimension (ie, pain intensity).
Thus, the results indicate that all else being equal, any of the 4
scales could be used for detecting changes in pain, although the
NRS and VAS might be considered first when particularly sensitive
and responsive measures of pain intensity are needed. Based on
other considerations, however, researchers and clinicians may
Table 2
Inter-scale correlation coefficients between the VAS, NRS, FPS-R, and VRS.
7°C5°C3°C1°C
VAS NRS FPS-R VAS NRS FPS-R VAS NRS FPS-R VAS NRS FPS-R
VAS––– ––– ––– –––
NRS 0.96 0.95 0.94 0.95
FPS-R 0.84 0.85 0.79 0.81 0.80 0.80 0.84 0.84
VRS 0.80 0.82 0.81 0.80 0.79 0.82 0.81 0.81 0.86 0.80 0.80 0.84
VAS, Visual Analogue Scale; NRS, Numerical Rating Scale; FPS-R, Faces Pain Scale-Revised; VRS, Verbal Rating Scale.
Table 3
Effect sizes (and number of participants required to obtain significant effects) for the VAS, NRS, FPS-R, and VRS.
Effect size (n)
VAS NRS FPS-R VRS
5°C3°C1°C5°C3°C1°C5°C3°C1°C5°C3°C1°C
7°C 0.22 (14) 0.47 (6) 0.58 (5) 0.25 (12) 0.49 (6) 0.59 (5) 0.20 (16) 0.44 (7) 0.55 (5) 0.17 (18) 0.42 (7) 0.58 (5)
5°C 0.20 (16) 0.46 (7) 0.22 (14) 0.48 (6) 0.20 (16) 0.45 (7) 0.17 (19) 0.29 (10)
3°C 0.30 (10) 0.36 (8) 0.20 (15) 0.29 (10)
VAS, Visual Analogue Scale; NRS, Numerical Rating Scale; FPS-R, Faces Pain Scale-Revised; VRS, Verbal Rating Scale.
Fig. 2. Average pain intensity ratings across temperatures. Error bars represent SD.
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elect to choose the NRS over the VAS in many settings. First,
although the NRS has not consistently been shown to have ratio
properties [43,45], its scores can provide data for parametric anal-
ysis [6,13,25,55]. Also, the NRS has been shown to be at least as
sensitive as the VAS, whether a 0–10 NRS or a 0–100 NRS is used
[6,9–11,24]. Third, the NRS is preferred over the VAS by patients
and clinicians for its relative simplicity and ease of administration
and scoring even when administered verbally [3,6,10,11,
13,20,24,55]. Fourth, the VAS tends to have higher failure rates
than the NRS or VRS, probably because both the NRS and the VRS
are very easy to understand and complete by patients
[3,6,10,11,13,20,24]. This latter point was also supported in the
current study, given our finding that the only participants excluded
from the sample for not being able to understand the measures
were excluded because they were unable to understand the VAS.
The VRS is a categorical measure that might not have ratio prop-
erties [43]. As a result, VRSs do not necessarily have equal intervals
between levels, which limits the conclusions that can be drawn
about the magnitude of differences over time or between patient
groups [25,26]. Also, when differences in responsivity are found,
VRSs, as well as the FPS-R, tend to be less sensitive than VAS and
NRS, consistent with the results from our study. This lower level
of responsivity may be related to the lower number of response
categories of these measures. However, we did find that both of
these scales were able to detect changes in pain associated with
differences in water temperature, indicating that they are valid
and could be used when responsivity is not a critical issue
[6,9,24,25,31]. Also, statisticians note that it is possible to draw va-
lid conclusions using parametric analysis with ordinal data, such as
data from VRSs, especially if number of categories in the scale is 5
or more [5,18,38]. Thus, the VRS can be considered a viable choice
in settings with patients or research subjects who might be less
able to use the NRS (eg, very young individuals or individuals with
significant cognitive impairment). Likewise, our findings provide
support for the validity of the FPS-R in adults, supporting its use
in clinical and research settings. Although the FPS-R has been
developed for use with children and proven useful with people
with cognitive and communication disabilities, there may be situ-
ations or settings in which it might be useful for other populations.
For example, the FPS-R might be useful for samples that include
both adults without cognitive impairment and children (or the el-
derly) in the same study, and a measure is needed that all partici-
pants can complete. The FPS-R might also be considered for use in
cross-cultural studies with adults, where researchers cannot be
certain of the meaning equivalence of the verbal endpoint descrip-
tors. In this situation, a measure based on facial expressions might
show a greater cultural equivalence.
Regarding sex effect on pain intensity ratings, our results are in
line with previous research showing significant sex effects on
intensity ratings following painful stimulation [34,35,51,54], with
women reporting higher pain intensity ratings across tempera-
tures. The sex effects were statistically significant for 3 of the scales
(NRS, VRS, FPS-R), and showed a nonsignificant trend for the VAS. It
is interesting to note that other researchers have not found sex
main effects when they used the VAS to test for these effects
[40,45]. These findings suggest the possibility that for experiments
specifically designed to test for or explain sex effects in pain inten-
sity, it might be best to avoid using the VAS.
One significant limitation of the study is that it was performed
with healthy young participants. Although it has been argued by
some that the cold-pressor test mimics the effects of chronic pain
conditions [40,53] due to its unpleasantness and to the fact that
the painful stimuli is conducted by the C fibers, which are impli-
cated in chronic pain, experimental pain is different from clinical
pain. Clinical pain, for example, is less predictable and controllable.
Also, participants in experimental pain studies can be assured that
the pain is not associated with any tissue damage, whereas pa-
tients with clinical pain cannot always be so sure of this. For these
reasons, clinical pain has an emotional significance and quality-of-
life implications that may influence pain perception [14]. There-
fore, the study findings do not necessarily generalize to patients
with clinical pain conditions. It would be useful to examine the rel-
ative responsivity of the 4 pain measures in response to treatments
or procedures known to impact clinical pain conditions to help
determine their generalizability.
Nevertheless, the findings provide support for the validity and
sensitivity of all 4 pain scales studied, with the exception that it
might be best to avoid the use of VAS in studies seeking to examine
sex effects. The findings also suggest that the NRS may be (very)
slightly more sensitive than the other measures in our sample of
individuals from Portugal; a finding consistent with some other
studies that have compared the NRS to other pain measures, and
supporting their cross-cultural reliability. Research is needed to
compare these measures in clinical settings to confirm the general-
izability of the current findings to clinical populations.
Conflict of interest statement
None of the authors have any conflicts of interest with respect
to this study.
Acknowledgements
The authors gratefully acknowledge José Elísio Pereira for his
contribution in the construction of the apparatus, and to Rita Ferre-
ira and Vera Melo for their assistance in data collection. M. Alexan-
dra Ferreira-Valente received PhD grant SFRH/BD/40956/2007 in
the past year from the Portuguese Foundation for Science and
Technology. José L. Pais Ribeiro received a sabbatical grant from
FCT (SFRH/BSAB/982/2010) between January and April 2010. Mark
P. Jensen received research support, consulting fees, or honoraria in
the past year from Analgesic Research, Consultants in Behavioral
Research, Endo, Fralex, Medtronic, Merck, Pfizer, Smith & Nephew,
US Department of Education, US Department of Veterans Affairs,
and the US National Institutes of Health.
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