Description
Write a 2 page paper (2 pages of TEXT, 1 inch margins, Times New Roman 12 point font, double spaced. You do not need an abstract or a title page) summarizing what the researchers did, what they found to be significant and interesting, any critical evaluations of their methods or findings, and your personal response to the article. The paper should be in your own words. You should not cut and paste any content from the article. Send your 2-page paper as a .docx or .doc file
837981
research-article2019
PSSXXX10.1177/0956797619837981Plaisier et al.The Timing of Weight Perception
ASSOCIATION FOR
PSYCHOLOGICAL SCIENCE
Research Article
When Does One Decide How Heavy an
Object Feels While Picking It Up?
Psychological Science
2019, Vol. 30(6) 822–829
© The Author(s) 2019
Article reuse guidelines:
sagepub.com/journals-permissions
https://doi.org/10.1177/0956797619837981
DOI: 10.1177/0956797619837981
www.psychologicalscience.org/PS
Myrthe A. Plaisier, Irene A. Kuling, Eli Brenner,
and Jeroen B. J. Smeets
Department of Human Movement Sciences, Vrije Universiteit Amsterdam
Abstract
When lifting an object, it takes time to decide how heavy it is. How does this weight judgment develop? To answer
this question, we examined when visual size information has to be present to induce a size-weight illusion. We found
that a short glimpse (200 ms) of size information is sufficient to induce a size-weight illusion. The illusion occurred not
only when the glimpse was before the onset of lifting but also when the object’s weight could already be felt. Only
glimpses more than 300 ms after the onset of lifting did not influence the judged weight. This suggests that it takes
about 300 ms to reach a perceptual decision about the weight.
Keywords
size-weight illusion, multisensory perception, time dependency, perceptual decision making
Received 6/22/18; Revision accepted 1/17/19
In order to make perceptual decisions about properties
in our environment, we combine sensory information
with expectations based on prior experience (Kersten,
Mamassian, & Yuille, 2004; Summerfield & de Lange,
2014). For instance, prior experience with one of an
object’s properties, such as its material or size, influences how heavy the object feels (Buckingham, 2014;
Buckingham, Cant, & Goodale, 2009; Buckingham &
Goodale, 2010a; de Brouwer, Smeets, & Plaisier, 2016;
Ellis & Lederman, 1998, 1999; Ross, 1969). The bestknown example of this is the size-weight illusion: a
large object is perceived to be lighter than a smaller
object of the same weight (for a recent review, see
Saccone & Chouinard, 2018). The size-weight illusion
is a robust effect that occurs even if the perceiver
knows that both objects have the same mass (Flournoy,
1894). It also occurs when heaviness is judged by pushing an object instead of lifting it (Plaisier & Smeets,
2012; Platkiewicz & Hayward, 2014), and it occurs when
size is felt instead of seen (Ellis & Lederman, 1993;
Plaisier & Smeets, 2015). As is the case with influences
of other priors, it is possible to alter the size-weight
illusion by training (Flanagan, Bittner, & Johansson,
2008). Size can affect perceived weight even if the
object is shown only prior to lifting (Buckingham &
Goodale, 2010b), suggesting that weight expectations
prior to lifting might play a role (but see Masin &
Crestoni, 1988, for counterevidence). Direct somatosensory information about an object’s weight becomes available as soon as the object loses contact with its supporting
surface. After more time passes, we reach a decision as
to how heavy the object feels. Our question is what is
the time course of this perceptual decision-making
process?
Prior to “liftoff,†the only information that one has
about an object’s mass are expectations based on what
it looks like and a statistical relation between its appearance and weight. After liftoff, the gravitational and inertial forces provide unambiguous sensory information
about the object’s mass. If seeing the size of the object
influences the judged weight because it provides an
expectation of the force required to achieve liftoff, it
should become much less effective as soon as expectations become irrelevant, that is, after the liftoff has
Corresponding Author:
Jeroen B. J. Smeets, Vrije Universiteit Amsterdam, Department of
Human Movement Sciences, Van der Boechorststraat 9, 1081 BT
Amsterdam, The Netherlands
E-mail: j.b.j.smeets@vu.nl
The Timing of Weight Perception
already occurred. If so, information about size presented
after liftoff should not influence the perceived weight.
Alternatively, if size information is considered throughout the judgment, there is no reason to expect the
moment of liftoff to have a special relevance, so presenting size information will remain effective until the decision has been made.
Perceptual decision making is usually studied in situations in which a choice needs to be made between
two alternatives (Shadlen & Kiani, 2013): a one-bit decision. Other judgments involve more alternatives, for
instance, three for judging the color of a traffic light or
four for judging the suit of a playing card. One can
interpret the number of bits of information as the number of binary decisions underlying the judgment (e.g.,
two bits for judging the suit of a playing card). Object
properties such as size or weight can vary on a continuous scale, so a judgment of such properties could
involve an infinite number of alternatives. However,
given the finite precision of such a judgment, one can
regard them as the outcome of a set of binary decisions,
with the number of decisions corresponding to the
relative precision expressed as bits of information (Fitts,
1954; Summerfield & de Lange, 2014).
The time needed for decisions that are more complex
than a binary decision is known to scale with the number of bits of information. For instance, choice reaction
times increase linearly with the number of bits of information processed (Hick, 1952; Hyman, 1953). Therefore, we can expect the time needed to reach a
perceptual decision on a continuous scale to increase
with the relative precision of the percept (expressed in
bits). Here, we monitored the process of judging an
object’s weight by varying the time at which visual
information about its size was made available during a
lifting action. Using three experiments that differed in
when participants were allowed to view the object they
were lifting and what happened after they lifted the
object, we determined the time course of when visual
size information can influence weight judgments.
Method
Participants
Ten participants (2 male; all right handed; age: M = 22
years, SD = 3) were recruited for Experiment 1. A second group of 10 participants (3 male; all right handed;
age: M = 28 years, SD = 3) was recruited for Experiment
2. A third group of 12 participants (6 male; 2 left
handed; age: M = 25 years, SD = 4) was recruited for
Experiment 3. Each participant only completed one
of the experiments. None of the participants was
aware of any relevant sensory or motor deficits. All
823
participants were naive as to the purpose of the experiments. They were treated in accordance with the local
ethical guidelines and gave informed consent prior to
participating. We used 10 participants on the basis of
earlier experience that this sample size allowed for an
easy detection of the illusion using the present stimuli
(Plaisier & Smeets, 2012). We included 2 more participants in Experiment 3 after observing the results of
Experiment 2. The study was part of a program that
was approved by the Scientific and Ethical Review
Board of the Faculty of Behavioural and Movement
Sciences of Vrije Universiteit Amsterdam.
Stimuli and setup
We used objects of two sizes: small (6 × 6 × 6 cm) and
large (6 × 6 × 9 cm; Fig. 1a). A plastic handle was
attached to the top of each object. We let participants
lift the objects by a handle so that they could not
deduce the size from the grip aperture when holding
the object. We made sure that wielding the object could
not provide information about its size (Amazeen &
Turvey, 1996; Kingma, van de Langenberg, & Beek,
2004) by connecting the handle to the object by a rotatable joint. In Experiment 1, we used two pairs of objects
(one pair of 260 g and one pair of 210 g, including the
handle); in Experiments 2 and 3, only the pair of objects
weighing 260 g was used. An infrared marker was
attached to the surface of each object at the center of
one side. Its position was tracked using an Optotrak
3020 system (Northern Digital, Waterloo, Ontario,
Canada). The objects were placed on a force sensor so
we could measure the lifting force (ATI Industrial Automation, Apex, NC; Nano17 F/T Sensor). The position
and force-sensor signals were sampled synchronously
at 500 Hz. Participants wore computer-controlled
PLATO visual-occlusion goggles (Translucent Technology, Toronto, Ontario, Canada).
Procedure
Participants were seated at a table with the occlusion
goggles closed. The experimenter placed an object in
front of the participant and indicated that he or she
could grasp the handle with the dominant hand. The
experimenter manually guided the participant’s hand
to the handle. Participants were instructed to wait while
holding the handle until an auditory go cue sounded.
At that moment, they were to lift the object straight up
without shaking or rotating it. In Experiments 1 and 2,
they subsequently placed it back on the table at a specific position. In Experiment 3, the experimenter
removed the object from the participant’s hand, so participants never moved the object down after lifting it.
Plaisier et al.
824
a
b
Experiment 1
No Vision
Force Sensor
Late Vision
c
Experiments 2 & 3
200-ms Vision
Continuous Vision
Fig. 1. Stimuli and procedure. Participants were asked to lift small and large objects (a) using handles connected to each object
by a hinge. Lifting objects in this way removed all haptic size cues. An infrared LED was attached to each object to track its
position. In Experiment 1, there were three conditions (b), which differed in the timing of when the occlusion goggles worn by
participants opened (the gray shading in the figure indicates when they were closed). In the two conditions in which the occlusion goggles opened, the object had to be placed on the square that corresponded to its size. Participants lifted the object off a
force sensor, allowing us to precisely determine the time of liftoff. In Experiment 2 (c), the procedure was largely the same as in
Experiment 1, except that the goggles opened for 200 ms at varying moments with respect to liftoff. The procedure for Experiment 3 (not illustrated) was the same as for Experiment 2, except that participants did not place the object back on the table.
If the object was to be placed on the table, participants
had to complete the whole movement within 3 s. Otherwise they had to reach maximum height within 2 s.
After completing each trial, participants were asked to
indicate the object’s weight using a method of free
magnitude estimation (Zwislocki & Goodman, 1980).
Participants performed 10 practice lifts to become
acquainted with the task prior to starting the main
experiment. Practice was performed with an object that
was not part of the stimulus set.
In Experiment 1, there were three conditions: no
vision, late vision, and continuous vision (Fig. 1b). In
the no-vision condition, the goggles remained closed
throughout the trial. In the late-vision condition, the
goggles opened as soon as the object was raised 5 mm
above the table surface. In the continuous-vision condition, the goggles opened roughly 0.5 s prior to the go
cue. This experiment consisted of three blocks of trials.
The first and third block each consisted of 20 no-vision
trials (5 per object). In these blocks, participants placed
the object on the table in front of them. In the second
block, participants performed a total of 80 late-vision
and continuous-vision trials (10 per object in each condition), which were randomly interleaved. During this
block of trials, drawings of a large and small square on
the table indicated on which side (left or right) to place
each object. Halfway through the block, these locations
were reversed. Participants placed the object at the
correct side on all trials so we could be sure that they
had taken note of the size of the object.
In Experiment 2 (Fig. 1c), the goggles opened for
200 ms during every trial. The moment at which the
goggles opened was varied with respect to the auditory
go cue. The goggles could open 200 ms prior to the go
cue or 100 ms, 400 ms, 700 ms, or 1,000 ms after the
go cue. Given the variability in response times, these
opening times resulted in a more or less uniform distribution of times of visual information relative to lift
The Timing of Weight Perception
onset throughout all phases of lifting. Each of the five
opening times was presented 10 times for both objects,
resulting in 100 trials per participant. Trials were performed in blocks, with one trial of each opening time
for each object randomly interleaved within each block
to ensure an even distribution of all opening times
throughout the experiment. Participants placed the
small object on the left and the large object on the right.
We did not switch left and right placement halfway
through, as in Experiment 1, because in this case the
goggles were always closed during this part of the trial.
Thus, participants could not see the drawings of the
small and large rectangles on the table and had to
remember where to place which object size. On average, participants did this correctly in 98.4% of the trials
(minimum individual trials correct was 92%).
Experiment 3 was identical to Experiment 2 except
that after lifting, participants did not place the object
back on the table but held it in the air until a second
auditory cue (2 s after the go cue) indicated that the
experimenter was going to remove it from their hand.
To ensure that participants noticed the size of the
object, we asked them to report whether it was a large
or a small object after giving their heaviness rating. On
average, participants judged the size correctly in 98.5%
of the trials (minimum was 93%).
Analysis
We first converted heaviness ratings into z scores for
each participant individually to be able to compare the
heaviness ratings across participants. To this end, we
took the heaviness ratings for all trials of an individual
participant and calculated the mean and standard deviation across all trials. To arrive at the z scores, we subtracted the mean from each heaviness rating and
divided the result by the standard deviation.
In Experiments 2 and 3, we determined the moment
of liftoff from the force-sensor signal with a method
that we adapted from the recommendation of Oostwoud
Wijdenes, Brenner, and Smeets (2014). We fitted a line
through the signal between 50% and 80% of the maximum force. We used this period because it was the
smoothest part of the force profile. We excluded a trial
if the R2 value of the fit was below .6 (this happened
in 1.8% of the trials in Experiment 2 and 3.1% of the
trials in Experiment 3). We took the intersection
between the fit line and a line at the level of no force
(the average of the last 100 samples during which there
was no object on the force sensor) as the moment of
liftoff. In the late-vision condition of Experiment 1, the
opening of the goggles happened 120 ms (betweenparticipants SD = 30) after the moment of liftoff that
was determined in this way.
825
In Experiment 1, we calculated a single illusion magnitude for each participant, object mass, and condition
by subtracting the z scores for the large object from
those for the small object of the same mass. We subsequently performed a repeated measures analysis of variance (ANOVA) on the illusion magnitude with object
mass and condition as factors. We followed this up with
post hoc paired-samples t tests to determine whether
the illusion magnitude differed between the conditions.
In all statistical tests, we considered p < .05 to be
significant.
In Experiments 2 and 3, we determined the time at
which the visual size information was provided (“time
of visual informationâ€Â) for each trial as the difference
between the time of liftoff and the center of the 200-ms
time window during which the goggles were open. We
subsequently transformed the heaviness ratings
(expressed as z scores) to smooth functions of the time
of visual information for each participant by calculating
a Gaussian weighted average for each instant and
object. The Gaussian function had a standard deviation
of 50 ms and was shifted in steps of 1 ms. Within the
range that we show in the figures, there was at least 1
data point within every 100-ms interval for each participant and object size. We calculated illusion magnitude as a function of time of visual size information for
each participant by subtracting the heaviness rating function for the large object from that for the small object.
In order to relate the heaviness ratings to the lifting
movement, we determined three parameters in addition
to the moment of liftoff: loading-phase onset, time of
half height, and time of maximum height. We used the
moment at which the loading force first exceeded 0.2
newton as the loading-phase onset. Time of half height
and time of maximum height were determined in a
straightforward manner from the Optotrak position signal. These two experiments were exploratory: No
hypotheses are tested; 95% confidence intervals around
the mean are provided as an indication of precision.
Results
In Experiment 1, we tested whether the size-weight
illusion occurs if size information is provided only
immediately after liftoff, when the decision process has
just started. As was to be expected, we did not find an
illusion in the no-vision condition, and we found a clear
illusion with continuous vision. Limiting vision to the
period after liftoff reduced the illusion to less than half
of its magnitude with continuous vision (late-vision
condition). A repeated measures ANOVA on the illusion
magnitude showed a significant effect of condition, F(2,
18) = 12.18, p < .001, η2 = .575, no effect of object mass,
and no interaction effects. Post hoc paired-samples t
Plaisier et al.
826
a
b
Illusion Magnitude (z score)
1
c
0.8
0.6
0.4
0.2
0
–0.2
Late Vision
Continuous
Vision
No Vision
Loading
–0.2
Half Height
0
0.2
Max Height
0.4
0.6
Time of Visual Information (s)
Loading
–0.2
Half Height
0
0.2
Max Height
0.4
0.6
Time of Visual Information (s)
Fig. 2. Results (averaged across participants). For Experiment 1 (a), the illusion magnitude is shown for each of the three conditions. Data
bars show means, circles indicate values for individual participants, and error bars show 95% confidence intervals. For Experiment 2 (b) and
Experiment 3 (c), the illusion magnitude is shown as a function of the time when visual information was provided with respect to liftoff.
The full illusion magnitude as found in the continuous-vision condition of Experiment 1 is indicated by the red dashed line. The gray horizontal bar indicates the loading phase, and the black dots indicate the moment at which the half height and maximum height were reached.
Shaded bands indicate 95% confidence intervals. Note that in Experiment 3, the full illusion effect did not occur for very late presentations
because participants did not place the object back on the table.
tests with Bonferroni correction showed a significant
difference between the no-vision and continuous-vision
conditions, t(9) = 4.12, p = .008, and between the latevision and continuous-vision conditions, t(9) = 3.94,
p = .010, but not between the late-vision and no-vision
conditions, t(9) = 1.55, p = .47. Thus, the size-weight
illusion decreased considerably when visual information about the object’s size was available only after the
decision process had started, so much so that performance was statistically indistinguishable from having
no visual size information.
Although the illusion effects in the late-vision and
the no-vision conditions were indistinguishable, we cannot conclude that visual size information was ignored
from the moment of liftoff, when the decision-making
process presumably started. The size of the illusion
effect and its associated 95% confidence interval in Figure 2a leave the possibility open that the illusion did
not disappear completely in the late-vision condition
(despite the magnitude not being significantly different
from that in the no-vision condition). It is possible that
visual information influenced perceived weight even
after liftoff up to a certain moment during the decisionmaking process. To test this hypothesis, we conducted
a more detailed investigation of how visually presenting
size information at different times during the decision
process influences the judged weight.
In Experiment 2, the goggles opened very briefly
(200 ms) once every trial. Despite this very short presentation of visual size information, the illusion was
strong. If visual size information was provided before
liftoff, the participants in Experiment 2 were influenced
by the short window of visual information to a similar
extent as the participants in Experiment 1 were influenced by continuous vision of the object (Fig. 2b; curve
slightly above the red dashed line). The illusion magnitude remained approximately the same when vision
was provided up to 300 ms after liftoff. Visual size
information thus influenced the perceived weight until
well after the start of the decision-making process.
The size-weight illusion was reliably lower than for
the full illusion in Experiment 1 only when the visual
size information was provided between 330 ms and 500
ms after liftoff (when the object had already reached
more than half of its maximal height). Surprisingly, the
illusion returned to its full magnitude when vision was
provided around 600 ms after liftoff, at about the
moment at which the maximum height was reached. At
that moment, the object was being held more or less
stationary in these trials, because participants were
waiting for the visual information to appear in order to
decide on which square they should place the object.
Possibly, the start of the downward movement induced
a reevaluation of the perceptual decision, which might
The Timing of Weight Perception
have been responsible for the illusion also occurring
in this situation.
In Experiment 3, we tested the robustness of our
results and investigated the occurrence of the illusion
when size information is provided very late without a
new movement possibly tempting one to reevaluate the
decision. To do so, we repeated Experiment 2 but without letting participants place the objects back on the
table. They were instructed to lift the object and hold
it in the air until the experimenter removed the object
from their hand. In Experiment 3, we replicated the
results of Experiment 2: The illusion decreased only
when vision was provided well after liftoff (Fig. 2c).
The illusion persisted for even slightly later moments
of providing visual size information than in Experiment
2 (up to 400 ms after liftoff). In line with our explanation for the reoccurrence of the illusion in Experiment
2, the illusion did not return to its full magnitude when
vision was provided later after liftoff.
Discussion
The size-weight illusion was markedly reduced when
visual size information became available only after liftoff in Experiment 1 (Fig. 2a), suggesting that the use
of prior information stopped when sensory input about
weight became available. By providing only a short
glimpse of visual information, we could determine the
timing at which this reduction occurred more precisely
in Experiments 2 and 3 (Figs. 2b and 2c). We found that
the illusion did continue to occur for visual information
that was provided briefly up to 400 ms after liftoff (Figs.
2b and 2c). We can thus conclude that information
related to prior experience affected the decisions well
after sensory input about weight became available and
thus after the decision-making process had started.
We can also conclude that the decision process took
at least 330 ms and 400 ms in Experiments 2 and 3,
respectively.
At first glance, this interpretation of Experiments 2
and 3 might seem inconsistent with the results of Experiment 1. In the late-vision condition of Experiment 1,
the illusion was considerably reduced when visual
information was continuously available after the object
had moved 5 mm upward, about 120 ms after liftoff. In
Experiments 2 and 3, we found a full-strength illusion
when visual information was provided briefly at that
time. This difference is probably due to the fact that
we did not control when participants determined the
size of the objects in Experiment 1 as precisely as we
did in Experiments 2 and 3. In the latter experiments,
participants had to look at the objects during the brief
exposure in order to know the size, while in Experiment 1, they could have looked at the object at any
time after the goggles opened and knew that they could
827
do so. This could be why the average illusion effect in
the late-vision condition of Experiment 1 was in
between no effect and a full-strength illusion.
In Experiment 2, the decision about weight appears
to have been reached 70 ms earlier than in Experiment
3. We argued in the introduction that the time needed
for a perceptual decision on a continuous scale depends
on the precision of the percept. If the perceptual decision was indeed made more quickly in Experiment 2
than in Experiment 3, one would expect that the participants in Experiment 2 would have been less precise
than those in Experiment 3. We therefore determined
the precision for each participant on the basis of the
variation of the responses for all trials for a single object
in which the visual information was provided before
liftoff. We indeed found that this coefficient was higher
(less precise) in Experiment 2 (coefficient of variation =
0.15) than in Experiment 3 (coefficient of variation =
0.12).
Our data show that it takes at least 330 ms to reach
a decision on how heavy an object feels. We cannot
exclude the possibility that the decision-making process
was still in progress after 330 ms. On the other hand,
one third of a second has been claimed to be the typical duration of embodied decisions (Ballard, Hayhoe,
Pook, & Rao, 1997). Is 330 ms indeed a reasonable time
for a perceptual decision of this precision? The observed
values for the coefficient of variation in the perceptual
judgments correspond to about three bits of information
(Welford, 1960). If the decision-making process would
indeed have finished at the moment visual information
about size ceased to have an effect, the informationprocessing capacity would have been about 10 bits per
second, which seems a reasonable value for human
sensorimotor processing (Fitts, 1954; Welford, 1960). So
it is likely that the time it took to reach a decision
indeed coincided with the time that visual information
had an effect after liftoff.
We interpreted the fact that visual information
affected weight perception for more than 300 ms after
the haptic information became available as indicating
that the indirect size information was combined with
haptic information to judge heaviness even when it was
presented considerably after direct weight information
became available. One could argue that this is not necessarily the case: If tactile information were processed
more than 300 ms slower than visual size information,
the visual size information might have been available
to the relevant parts of the brain before the haptic
weight information. We consider this to be unlikely
because tactile information is known to be processed
within 100 ms to stabilize the grasp ( Johansson &
Flanagan, 2009). It is known that the judged timing of
signals can shift to some extent with repeated exposure
when judging simultaneity (Sugita & Suzuki, 2003), but
Plaisier et al.
828
it is also known that we do not correct for processingtime differences when using signals to control goaldirected movements (van Mierlo, Louw, Smeets, &
Brenner, 2009), so we may also not adjust the timing for
making judgments on the basis of lifting movements.
Even if the timing of signals would be shifted, it is very
unlikely that such a shift would influence our conclusions
substantially, as reported shifts were less than 100 ms.
Note that in the above-mentioned cue-combination studies, the temporal-integration window was also clearly less
than 100 ms, so a sluggish temporal integration also cannot explain our finding that visual information presented
300 ms after liftoff affected heaviness ratings.
There are two approaches to explain the size-weight
illusion: a top-down and a bottom-up approach. The
top-down approach involves expectations (Buckingham, 2014; Ross, 1969), quantified as anti-Bayesian
(Brayanov & Smith, 2010) or Bayesian priors (Peters,
Ma, & Shams, 2016). Our results are clearly in conflict
with such explanations because the visual information
that is supposed to set the prior was just as effective
when it was presented after the haptic information. The
results are in line with an explanation in terms of a
bottom-up combination of a direct and an indirect cue
(Anderson, 1970; Masin & Crestoni, 1988). For this
approach, one needs to identify the indirect cue. One
suggestion is that object density is this indirect cue
(Wolf, Bergman Tiest, & Drewing, 2018). However, the
size-weight illusion is equally strong for objects that
differ in size but clearly not in amount of material and
thus not in density (Plaisier & Smeets, 2015). So this
explanation of the size-weight illusion is still lacking a
convincing candidate for the indirect cue.
In summary, our results show that perceptual decisions can be affected by prior knowledge that is invoked
at a moment at which direct sensory information is
already available. However, once a perceptual decision
has been reached, prior knowledge does not lead to a
reevaluation of the decision. Changes in direct sensory
information, for instance due to a new motor action,
could lead to reevaluation of the decision, in which
recently invoked prior knowledge is also considered.
Overall, this study provides a first account of the time
course of the use of prior knowledge in making perceptual decisions on a continuous scale.
Action Editor
Philippe G. Schyns served as action editor for this article
Author Contributions
M. A. Plaisier and I. A. Kuling conceived the experiments and
discussed the experimental design with E. Brenner and J. B. J.
Smeets. M. A. Plaisier and I. A. Kuling performed the experiments. M. A. Plaisier analyzed the data and drafted the
manuscript. All authors reviewed the manuscript and
approved the final version for submission.
ORCID iD
Jeroen B. J. Smeets
https://orcid.org/0000-0002-3794-0579
Declaration of Conflicting Interests
The author(s) declared that there were no conflicts of interest
with respect to the authorship or the publication of this
article.
Funding
This research
for Scientific
M. A. Plaisier
grant (12160)
was supported by a Netherlands Organisation
Research Veni grant (MaGW 451-12-040) to
and by a Dutch Technology Foundation STW
to J. B. J. Smeets.
Open Practices
Design and analysis plans for the experiments reported in
this article were not formally preregistered. All data underlying Figure 2 have been made publicly available via the Open
Science Framework and can be accessed at http://osf.io/6e9bv.
All other data and materials for the experiments have not been
made publicly available.
References
Amazeen, E. L., & Turvey, M. T. (1996). Weight perception and the haptic size-weight illusion are functions of
the inertia tensor. Journal of Experimental Psychology:
Human Perception and Performance, 22, 213–232.
Anderson, N. H. (1970). Averaging model applied to the
size-weight illusion. Perception & Psychophysics, 8, 1–4.
doi:10.3758/bf03208919
Ballard, D. H., Hayhoe, M. M., Pook, P. K., & Rao, R. P. N.
(1997). Deictic codes for the embodiment of cognition.
Behavioral & Brain Sciences, 20, 723–742.
Brayanov, J. B., & Smith, M. A. (2010). Bayesian and “anti-Bayesian†biases in sensory integration for action and perception in the size-weight illusion. Journal of Neurophysiology,
103, 1518–1531. doi:10.1152/jn.00814.2009
Buckingham, G. (2014). Getting a grip on heaviness perception: A review of weight illusions and their probable
causes. Experimental Brain Research, 232, 1623–1629.
doi:10.1007/s00221-014-3926-9
Buckingham, G., Cant, J. S., & Goodale, M. A. (2009). Living
in a material world: How visual cues to material properties affect the way that we lift objects and perceive their
weight. Journal of Neurophysiology, 102, 3111–3118.
Buckingham, G., & Goodale, M. A. (2010a). The influence
of competing perceptual and motor priors in the context
of the size-weight illusion. Experimental Brain Research,
205, 283–288.
Buckingham, G., & Goodale, M. A. (2010b). Lifting without
seeing: The role of vision in perceiving and acting upon
the size weight illusion. PLOS ONE, 5(3), Article e9709.
doi:10.1371/journal.pone.0009709
The Timing of Weight Perception
de Brouwer, A. J., Smeets, J. B. J., & Plaisier, M. A. (2016).
How heavy is an illusory length? i-Perception, 7(5).
doi:10.1177/2041669516669155
Ellis, R. R., & Lederman, S. J. (1993). The role of haptic versus
visual volume cues in the size-weight illusion. Perception
& Psychophysics, 53, 315–324.
Ellis, R. R., & Lederman, S. J. (1998). The golf-ball illusion:
Evidence for top-down processing in weight perception.
Perception, 27, 193–201.
Ellis, R. R., & Lederman, S. J. (1999). The material-weight illusion revisited. Perception & Psychophysics, 61, 1564–1576.
Fitts, P. M. (1954). The information capacity of the human
motor system in controlling the amplitude of movement. Journal of Experimental Psychology, 47, 381–391.
doi:10.1037/h0055392
Flanagan, J. R., Bittner, J. P., & Johansson, R. S. (2008).
Experience can change distinct size-weight priors engaged
in lifting objects and judging their weights. Current
Biology, 8, 1742–1747. doi:10.1016/j.cub.2008.09.042
Flournoy, T. (1894). De l’influence de la perception visuelle
des corps sur leur poids apparent [The influence of visual
perception on the apparent weight of objects]. L’ Annee
Psychologique, 1, 198–200.
Hick, W. E. (1952). On the rate of gain of information. The
Quarterly Journal of Experimental Psychology, 4, 11–26.
doi:10.1080/17470215208416600
Hyman, R. (1953). Stimulus information as a determinant of
reaction time. Journal of Experimental Psychology, 45,
188–196. doi:10.1037/h0056940
Johansson, R. S., & Flanagan, J. R. (2009). Coding and use
of tactile signals from the fingertips in object manipulation tasks. Nature Reviews Neuroscience, 10, 345–359.
doi:10.1038/nrn2621
Kersten, D., Mamassian, P., & Yuille, A. (2004). Object perception as Bayesian inference. Annual Review of Psychology,
55, 271–304. doi:10.1146/annurev.psych.55.090902.142005
Kingma, I., van de Langenberg, R., & Beek, P. J. (2004).
Which mechanical invariants are associated with the perception of length and heaviness of a nonvisible handheld rod? Testing the inertia tensor hypothesis. Journal
of Experimental Psychology: Human Perception and
Performance, 30, 346–354. doi:10.1037/0096-1523.30.2.346
Masin, S. C., & Crestoni, L. (1988). Experimental demonstration of the sensory basis of the size-weight illusion.
Perception & Psychophysics, 44, 309–312.
Oostwoud Wijdenes, L., Brenner, E., & Smeets, J. B. J. (2014).
Analysis of methods to determine the latency of online
829
movement adjustments. Behavior Research Methods, 46,
131–139. doi:10.3758/s13428-013-0349-7
Peters, M. A. K., Ma, W. J., & Shams, L. (2016). The sizeweight illusion is not anti-Bayesian after all: A unifying
Bayesian account. PeerJ, 4, Article e2124. doi:10.7717/
peerj.2124
Plaisier, M. A., & Smeets, J. B. J. (2012). Mass is all that matters in the size-weight illusion. PLOS ONE, 7(8), Article
e42518. doi:10.1371/journal.pone.0042518
Plaisier, M. A., & Smeets, J. B. J. (2015). Object size can influence perceived weight independent of visual estimates
of the volume of material. Scientific Reports, 5, Article
17719. doi:10.1038/srep17719
Platkiewicz, J., & Hayward, V. (2014). Perception-action dissociation generalizes to the size-inertia illusion. Journal
of Neurophysiology, 111, 1409–1416. doi:10.1152/jn
.00557.2013
Ross, H. E. (1969). When is weight not illusory? The Quarterly
Journal of Experimental Psychology, 21, 346–355.
Saccone, E. J., & Chouinard, P. A. (2018). The influence of
size in weight illusions is unique relative to other object
features. Psychonomic Bulletin & Review. Advance online
publication. doi:10.3758/s13423-018-1519-5
Shadlen, M. N., & Kiani, R. (2013). Decision making as a
window on cognition. Neuron, 80, 791–806. doi:10.1016/j
.neuron.2013.10.047
Sugita, Y., & Suzuki, Y. (2003). Implicit estimation of soundarrival time. Nature, 421, 911. doi:10.1038/421911a
Summerfield, C., & de Lange, F. P. (2014). Expectation in
perceptual decision making: Neural and computational
mechanisms. Nature Reviews Neuroscience, 15, 745–756.
doi:10.1038/nrn3838
van Mierlo, C. M., Louw, S., Smeets, J. B. J., & Brenner, E.
(2009). Slant cues are processed with different latencies
for the online control of movement. Journal of Vision,
9(3), Article 25. doi:10.1167/9.3.25
Welford, A. T. (1960). The measurement of sensory-motor performance: Survey and reappraisal of twelve years’ progress. Ergonomics, 3, 189–230. doi:10.1080/0014013600
8930484
Wolf, C., Bergman Tiest, W. M., & Drewing, K. (2018). A
mass-density model can account for the size-weight illusion. PLOS ONE, 13(2), Article e0190624. doi:10.1371/
journal.pone.0190624
Zwislocki, J. J., & Goodman, D. A. (1980). Absolute scaling of sensory magnitudes: A validation. Perception &
Psychophysics, 28, 28–38.
835147
research-article2019
PSSXXX10.1177/0956797619835147StavrovaLife Satisfaction and Mortality
ASSOCIATION FOR
PSYCHOLOGICAL SCIENCE
Short Report
Having a Happy Spouse Is Associated
With Lowered Risk of Mortality
Psychological Science
2019, Vol. 30(5) 798–803
© The Author(s) 2019
Article reuse guidelines:
sagepub.com/journals-permissions
https://doi.org/10.1177/0956797619835147
DOI: 10.1177/0956797619835147
www.psychologicalscience.org/PS
Olga Stavrova
Department of Social Psychology, Tilburg University
Abstract
Studies have shown that individuals’ choice of a life partner predicts their life outcomes, from their relationship
satisfaction to their career success. The present study examined whether the reach of one’s spouse extends even further,
to the ultimate life outcome: mortality. A dyadic survival analysis using a representative sample of elderly couples
(N = 4,374) followed for up to 8 years showed that a 1-standard-deviation-higher level of spousal life satisfaction was
associated with a 13% lower mortality risk. This effect was robust to controlling for couples’ socioeconomic situation
(e.g., household income), both partners’ sociodemographic characteristics, and baseline health. Exploratory mediation
analyses pointed toward partner and actor physical activity as sequential mediators. These findings suggest that life
satisfaction has not only intrapersonal but also interpersonal associations with longevity and contribute to the fields of
epidemiology, positive psychology, and relationship research.
Keywords
life satisfaction, mortality, dyadic analyses, couples, open materials
Received 8/2/18; Revision accepted 12/30/18
Research has consistently shown that life satisfaction is
associated with longevity (for a review, see Diener &
Chan, 2011). For example, meta-analyses of long-term
prospective studies have shown that higher life satisfaction predicts lower risk of mortality over decades (Chida
& Steptoe, 2008). Although this literature has demonstrated an intrapersonal effect of life satisfaction (i.e.,
an effect of an individual’s life satisfaction on that individual’s mortality), it is less clear whether life satisfaction has interpersonal effects as well. In particular, does
an individual’s life satisfaction affect the mortality risk
of his or her spouse?
Epidemiological studies have demonstrated the importance of contextual characteristics (e.g., neighborhood
characteristics; Bosma, Dike van de Mheen, Borsboom,
& Mackenbach, 2001) for individuals’ longevity. Adopting
the interpersonal perspective (Zayas, Shoda, & Ayduk,
2002), I propose that the characteristics (e.g., life satisfaction) of the people who are close to an individual can
also make up that person’s context and, potentially,
affect his or her life outcomes. For example, life satisfaction has been associated with healthy behaviors such
as physical exercise (Kim, Kubzansky, Soo, & Boehm,
2017). Given that spouses tend to affect each other’s
lifestyle ( Jackson, Steptoe, & Wardle, 2015), having a
happy spouse might increase one’s likelihood of engaging in healthy behaviors. In addition, happiness has been
associated with helping behavior (O’Malley & Andrews,
1983). Hence, having a happy partner might be related
to experiencing support from that partner and, consequently, might improve one’s health and longevity.
Indeed, a recent study found that spousal life satisfaction was associated with individuals’ self-rated health
(Chopik & O’Brien, 2017), although such interpersonal
effects were not detected for doctor-diagnosed chronic
conditions (Chopik & O’Brien, 2017) or for inflammation
markers (Uchino et al., 2018). None of the existing studies
have explored whether spousal life satisfaction predicts
individuals’ mortality. The present research examined this
question using panel data of approximately 4,400 elderly
couples in the United States. In addition, a set of
Corresponding Author:
Olga Stavrova, Department of Social Psychology, Tilburg University,
Warandelaan 2, 5000 LE, Tilburg, The Netherlands
E-mail: O.Stavrova@uvt.nl
Life Satisfaction and Mortality
exploratory mediation analyses tested the role of partner
support as well as partner and actor physical activity as
potential mechanisms for such an association.
Finally, it is possible that the level of spousal life
satisfaction per se matters much less than the extent to
which it is similar to individuals’ own life satisfaction.
A growing body of research has underscored the level
of congruence between partners’ dispositional characteristics as an important factor for their relationship and
life outcomes (Dyrenforth, Kashy, Donnellan, & Lucas,
2010). Therefore, in an additional set of analyses, I
explored whether the level of actor-partner similarity
in life satisfaction was associated with actor mortality.
Method
Participants
The data for this study came from the Health and Retirement Study (HRS; http://hrsonline.isr.umich.edu/), a
nationally representative panel study of American
adults ages 50 and older and their spouses. It is sponsored by the National Institute on Aging (Grant No. NIA
U01AG009740) and is conducted by the University of
Michigan. HRS is particularly well suited for the present
investigation because it collects data from both spouses.
Starting in 2006, the study has included a measure of
life satisfaction, as part of a self-report questionnaire
that participants are asked to complete on their own
and return by mail. For one half of the sample, life satisfaction was first measured in 2006, and for the other
half, it was first measured in 2008. These data were
combined into a baseline assessment. I selected participants who had a spouse or a live-in partner at baseline
(95.7% of the participants who had a live-in partner
were officially married).1 After I removed cases with
missing values on key variables (actor life satisfaction,
partner life satisfaction, survival time), the final sample
consisted of 8,748 individuals (mean age at baseline =
67.17, SD = 9.75; 50.0% male). This sample size was large
enough for even small effects to be detected with 80%
power (at α = .05). Of the 4,374 couples, 99.5% were
heterosexual. Data from participants who remained alive
throughout the observation period (n = 6,643) or were
lost to follow-up (n = 656) were censored.2
The data and materials for HRS can be accessed at its
Website (http://hrsonline.isr.umich.edu/). The computer
code for the analyses reported here can be accessed at
the Open Science Framework (https://osf.io/geq9x/).
Measures
Life satisfaction. Life satisfaction was measured with
the Satisfaction With Life Scale (Diener, Emmons, Larsen,
& Griffin, 1985). This scale includes five items (e.g., “I am
799
satisfied with my lifeâ€Â). Because a 6-point response scale
was used in 2006 and a 7-point response scale was used
in 2008 (both scales ranged from strongly disagree to
strongly agree), I rescaled the responses to range from 1
to 10.3 The scale had good reliability (2006 subsample:
α = .89; 2008 subsample: α = .88). The analyses included
both partner and actor life satisfaction.
Mortality. The HRS data set included information on
participants’ vital status (1 = deceased, 0 = alive) through
December 2014. This information came from the National
Death Index (Centers for Disease Control and Prevention,
2017), the spouse’s report, or both. Survival time was
computed in months, starting from the month of the
baseline interview and ending with death or censoring
(in December 2014).
Additional variables. Perceived partner support was
measured by participants’ ratings of the extent to which
their partners provided them with social support (seven
items; e.g., “How much can you rely on [your partner] if
you have a serious problem?†“How much can you open
up to [your partner] if you need to talk about your worries?†“How much does [your partner] let you down when
you are counting on him/her?â€Â; all items are provided in
the Supplemental Material available online). Responses
were given on a 4-point scale (1 = a lot, 4 = not at all)
and were recoded such that higher values reflected stronger support. Each person’s recoded responses were then
averaged (2006 subsample: α = .82; 2008 subsample: α =
.84).
Actor and partner physical activity were assessed
with two questions. Both partners indicated how often
they engaged in vigorous activities (e.g., jogging,
cycling, digging with a spade or shovel) and moderately
energetic activities (e.g., gardening, cleaning the car,
walking at a moderate pace, dancing). Responses to
both questions were given on a 4-point scale (1 = more
than once a week, 2 = once a week, 3 = one to three
times a month, 4 = hardly ever or never) and were
recoded such that higher values reflected higher frequency. The frequencies of vigorous and moderately
energetic activity were related to each other (r = .36,
p < .001), so I combined the responses to these two
questions to form an indicator of physical activity.
To make sure that any observed association between
partner life satisfaction and actor mortality was not
driven by an overlap with sociodemographic characteristics or baseline health (e.g., one spouse’s health
problems might negatively affect both spouses’ life satisfaction and mortality), I included a range of control
variables in the analyses. Specifically, I controlled for
actor and partner self-rated health (1 = poor, 5 = excellent), as well as morbidity, measured with the number of
doctor-diagnosed chronic conditions (hypertension,
800
diabetes, cancer, lung disease, coronary heart disease,
stroke, arthritis, incontinence, psychiatric problems;
although this list is not comprehensive, it covers major
causes of death). Further control variables included
actor gender (1 = male, 0 = female), actor and partner
age at baseline, actor and partner ethnicity (1 =
Caucasian, 0 = other), actor and partner education (1 =
less than high school, 2 = general education diploma,
3 = high school diploma, 4 = some college, 5 = college
and above), and baseline year (1 = 2008, 0 = 2006). Given
that the household financial situation is likely to affect
both partners’ life satisfaction and longevity, the analyses
also included baseline household income (total annual
household income in dollars, log transformed). To
account for partner mortality, the analyses included a
variable indicating whether the partner died during the
observation period (1 = deceased, 0 = alive).
Results
Means and standard deviations of the variables, as well
as their zero-order correlations, are provided in Table
S1 in the Supplemental Material. During the observation
period, 16.6% (n = 1,449) of the sample died. The survival time ranged from 2 to 104 months (8.67 years)
and averaged 50.5 months (4.21 years). An examination
of differences between survivors and decedents
revealed that the latter were older, t(8746) = 33.57, p <
.001; were more likely to be male, Ç2(1, N = 8,748) =
191.90, p < .001; were less educated, t(8745) = 11.33,
p < .001; and were less wealthy, t(2703) = 14.43, p <
.001. They also were more likely to have chronic diseases, t(1955) = 20.66, p < .001; were less likely to
engage in physical activity, t(8591) = 17.84, p < .001;
and reported poorer self-rated health, t(1959) = 23.51,
p < .001, and lower life satisfaction, t(1976) = 6.55, p <
.001. Similarly, decedents’ spouses, compared with survivors’ spouses, were older, t(8746) = 24.53, p < .001;
were less educated, t(2031) = 9.70, p < .001; reported
more chronic conditions, t(8745) = 11.00, p < .001;
reported a lower level of physical activity, t(8591) = 10.91,
p < .001; and had poorer self-rated health, t(8741) = 8.13,
p < .001. They also reported lower relationship satisfaction, t(1922) = 7.97, p < .001, and lower life satisfaction,
t(1986) = 5.09, p < .001. Finally, decedents’ spouses were
more likely than survivors’ spouses to die within the
observation period, Ç2(1, N = 8,748) = 202.61, p < .001.
To determine whether partner life satisfaction predicted actor mortality, I used multilevel (dyadic) survival analysis. Specifically, because time was measured
on a continuous scale (in months), I used the Cox
proportional hazards model. Given the clustered timeto-event data (individuals were clustered within dyads),
I used an extension of the Cox model that accounts for
Stavrova
correlated observations by implementing robust sandwich variance estimators. The analyses were conducted
with the survival package (Therneau, 2015) in R. Note
that using a frailty model with penalized likelihood
estimation produced the same results (see Table S4 in
the Supplemental Material).
Time to event was measured in months, from the
baseline measurement of life satisfaction until death or
censoring. I additionally checked for robustness of the
results by conducting analyses using participants’ age
as a time scale. These analyses provided the same
results and are reported in the Supplemental Material
(Table S4). All continuous variables were standardized
before analysis, so the coefficients can be interpreted
in terms of standard deviations.
The full estimation results are presented in Table S2 in
the Supplemental Material. Model 1 showed that greater
partner life satisfaction at baseline was associated with
lower actor mortality risk. Specifically, a 1-standarddeviation-higher level of spousal life satisfaction was associated with a 13% lower risk of dying within the following
8 years (hazard ratio, or HR = 0.87, 95% confidence interval, or CI = [0.83, 0.91], p < .001). Figure 1 plots the
cumulative hazard of death during the observation period,
separately for individuals with a happy spouse (life satisfaction above the median) and individuals with an
unhappy spouse (life satisfaction below the median). The
figure shows that as time went by, the mortality risk of
individuals with a happy spouse rose more slowly than
the mortality risk of individuals with an unhappy spouse.
To make sure that this effect was not just a result of
confounding with participants’ own life satisfaction, I
added actor life satisfaction at baseline in Model 2 (see
Table S2 in the Supplemental Material). The results
showed that both greater actor life satisfaction at baseline (HR = 0.86, 95% CI = [0.82, 0.91], p < .001) and
greater partner life satisfaction at baseline(HR = 0.92,
95% CI = [0.87, 0.97], p = .001) were associated with
lower mortality risk.
Model 3 (see Table S2 in the Supplemental Material)
showed that these effects were robust to controlling for
major sociodemographic variables: actor gender, actor
and partner age, actor and partner ethnicity, actor and
partner education level, household income, baseline
year, and couple type (same-sex vs. heterosexual 4). A
1-standard deviation-higher level of actor life satisfaction was associated with an 18% lower mortality risk
(HR = 0.82, 95% CI = [0.78, 0.86], p < .001), and a
1-standard deviation-higher level of partner life satisfaction was associated with a 10% lower mortality risk
(HR = 0.90, 95% CI = [0.85, 0.95], p < .001).
In Model 4, I added actor and partner health indicators (self-rated health and morbidity) and partner mortality (whether the partner died during the observation
Life Satisfaction and Mortality
801
Partner Life Satisfaction Below Median
Partner Life Satisfaction Above Median
0.25
Cumulative Hazard
0.20
+
0.15
+
0.10
0.05
0.00
0
25
50
75
100
Survival Time (Months Since Baseline)
Fig. 1. Cumulative hazard of death (including 95% confidence
bands) during the observation period. Results are shown separately
for individuals whose spouses reported life satisfaction below the
median at baseline and those whose spouses reported life satisfaction
above the median at baseline.
period). The effect of actor life satisfaction on actor
mortality was rendered nonsignificant (HR = 0.96, 95%
CI = [0.90, 1.02], p = .155). In contrast, the effect of
partner life satisfaction remained (HR = 0.92, 95% CI =
[0.87, 0.97], p = .005).
Similarity effect
To explore whether the level of actor-partner similarity
in life satisfaction was associated with actor mortality,
I used a dyadic polynomial regression analysis, the
state-of-the-art approach to testing similarity effects
(Weidmann, Schönbrodt, Ledermann, & Grob, 2017).
Actor mortality was regressed on actor and partner life
satisfaction (xa and xp), their interaction term (x axp),
and the quadratic terms (xa2 and xp2). The quadratic
and interaction terms were not significant (ps > .57).
The only terms with significant effects were the linear
terms of actor life satisfaction (HR = 0.85, 95% CI = [0.79,
0.92], p < .001) and partner life satisfaction (HR = 0.93,
95% CI = [0.86, 0.996], p = .039). Hence, I concluded
that the data do not provide evidence for a similarity
effect. Overall, these results suggest that having a partner who is more satisfied with life is associated with
lower mortality regardless of one’s own level of life
satisfaction.
Exploratory mediation analyses
The variables available in the data set allowed me to
explore two potential mediation processes. First, I
hypothesized that individuals with a happier partner
experience more partner support, and that greater perceived partner support is associated with lower mortality. However, an examination of the zero-order
associations among partner life satisfaction, perceived
partner support, and actor mortality revealed that this
mediation path is unlikely: Although having a happier
partner was indeed associated with greater perceived
partner support (r = .27, 95% CI = [.25, .29], p < .001),
perceived partner support was not related to actor mortality (HR = 0.99, 95% CI = [0.94, 1.04], p = .69).
Second, I explored the role of partner and actor
physical activity as sequential mediators. Specifically,
on the basis of previous research (Kim et al., 2017), I
hypothesized that greater partner life satisfaction is
associated with increased partner physical activity,
which in turn is associated with greater actor physical
activity ( Jackson et al., 2015) and, consequently, lower
actor mortality. A look at the zero-order associations
showed that, indeed, partner life satisfaction was positively associated with partner physical activity (r = .17,
95% CI = [.15, .19], p < .001), partner and actor physical
activity were positively related to each other (r = .24,
95% CI = [.22, .26], p < .001), and actor physical activity
negatively predicted actor mortality (HR = 0.75, 95%
CI = [0.71, 0.79], p < .001).
Therefore, I proceeded to test for sequential mediation using multilevel structural equation modeling.
The model (see Fig. S1 in the Supplemental Material
included a set of multilevel (participants nested within
couples) regression equations, in which partner life
satisfaction predicted partner physical activity (path
a, multilevel linear regression), partner physical activity predicted actor physical activity (path d, multilevel
linear regression), and actor physical activity predicted actor mortality (path b, multilevel Cox regression). The indirect effect was computed by multiplying
the a, d, and b paths, and its significance was tested
using the delta method. The model included random
intercepts for actor and partner physical activity and
actor mortality and used clustered robust standard
errors. The analyses were conducted with Stata/MP
Version 14.2.
The results showed that partner life satisfaction was
positively associated with partner physical activity (b =
0.08, 95% CI = [0.07, 0.09], p < .001), which in turn was
positively associated with actor physical activity (b =
0.23, 95% CI = [0.20, 0.26], p < .001), which was negatively associated with actor mortality (HR = 0.64, 95%
CI = [0.61, 0.68], p < .001). The coefficient for the
indirect effect was significant, b = −0.008, 95% CI =
[−0.01, −0.006], p < .001, which provided support to the
sequential mediation. The indirect effect was robust to
adding the control variables as predictors of both the
mediators and the dependent variable (see Table S5 in
the Supplemental Material).
Stavrova
802
Exploratory moderation analyses
I explored whether the effect of partner life satisfaction
on actor mortality depended on various actor and partner characteristics: gender, age, ethnicity, education,
income, health indicators, physical activity, perceived
partner support, and partner mortality. I ran 16 models
testing the interactions between partner life satisfaction
and these variables (by adding the respective interaction
terms, one at a time, to Model 4; see Table S2 in the
Supplemental Material). The only significant interaction
was between partner life satisfaction and partner mortality (HR = 1.15, 95% CI = [1.02, 1.31], p = .027). Partner
life satisfaction was negatively associated with actor
mortality only when the partner remained alive through
the end of the observation period (partner alive: HR =
0.90, 95% CI = [0.83. 0.96], p = .003; partner deceased:
HR = 1.03, 95% CI = [0.93, 1.15], p = .553). Yet the
exploratory nature of these analyses and the multiple
testing do not allow strong conclusions to be drawn.
Discussion
Previous research has shown that individuals’ career
success and relationship and life satisfaction are predicted by their spouses’ dispositional characteristics
(Dyrenforth et al., 2010; Solomon & Jackson, 2014). The
present research suggests that spouses’ reach might
extend even further. A dyadic survival analysis using
the data from 4,374 couples showed that having a
spouse who was more satisfied with life was associated
with reduced mortality.
What explains this interpersonal effect of life satisfaction? Exploratory mediation analyses established
partner and actor physical activity as sequential mediators. One partner’s life satisfaction was associated with
his or her increased physical activity, which in turn was
related to increased physical activity in the other partner, which predicted that partner’s mortality. Yet, given
the correlational nature of these data, these results
should be interpreted with caution.
It is noteworthy that the effect of spousal life satisfaction was comparable in size to the effects of other
well-established predictors of mortality, such as education and income (in the present study, HRs = 0.90 for
partner life satisfaction, 0.93 for household income, and
0.91 for actor education). In fact, spousal life satisfaction predicted mortality as strongly as (and even more
robustly than) an individual’s own life satisfaction and
as strongly as basic personality traits, such as neuroticism and extraversion, predicted mortality in previous
work ( Jokela et al., 2013).
Although most existing research on predictors of
mortality has focused nearly exclusively on individuals’
own characteristics, the present analyses revealed that
the characteristics of a person who is close to an
individual, such as a spouse, might be an equally
important determinant of that individual’s mortality.
Continuing this line of research, future studies might
explore whether the interpersonal effect of life satisfaction on mortality is restricted to (marital) dyads or
whether it extends to larger social networks.
To conclude, happiness is a desirable trait in a
romantic partner, and marriage to a happy person is
more likely to last than is marriage to an unhappy person (Lucas, 2005). The present study showed that having a happier spouse is associated not only with a
longer marriage but also with a longer life.
Action Editor
James K. McNulty served as action editor for this article.
Author Contributions
O. Stavrova is the sole author of this article and is responsible
for its content.
ORCID iD
Olga Stavrova
https://orcid.org/0000-0002-6079-4151
Acknowledgments
I would like to thank Anthony M. Evans for his statistical
advice and general support.
Declaration of Conflicting Interests
The author(s) declared that there were no conflicts of interest
with respect to the authorship or the publication of this
article.
Supplemental Material
Additional supporting information can be found at http://
journals.sagepub.com/doi/suppl/10.1177/0956797619835147
Open Practices
All analysis code for this study has been made publicly available via the Open Science Framework and can be accessed
at https://osf.io/geq9x/. The data are available through the
Health and Retirement Study’s Web site (http://hrsonline.isr
.umich.edu/). The design and analysis plans for this study were
not preregistered. The complete Open Practices Disclosure for
this article can be found at http://journals.sagepub.com/doi/
suppl/10.1177/0956797619835147. This article has received the
badge for Open Materials. More information about the Open
Practices badges can be found at http://www.psychological
science.org/publications/badges.
Notes
1. Additional analyses using only married couples produced
identical results (see Table S4 in the Supplemental Material).
Life Satisfaction and Mortality
2. These two groups of censored observations did not differ from each other on any variable included in the analyses,
except for the number of chronic conditions: Participants who
dropped out reported fewer chronic conditions (M = 1.87, SD =
1.40) than did participants who stayed in the panel (M = 2.07,
SD = 1.46), t(7296) = 3.46, p = .001.
3. As a robustness check, I used standardization to normalize
the data instead (i.e., I standardized the values within the two
subsamples). The analyses using the standardized scale produced the same results as the analyses presented in the main
text (see Table S3 in the Supplemental Material).
4. Being part of a same-sex couple positively predicted mortality (HR = 2.72, p = .018; there were 9 gay and 11 lesbian couples
in the sample). The interaction between couple type (gay vs.
lesbian) and actor gender was not significant (HR = 0.38, p =
.260).
References
Bosma, H., Dike van de Mheen, H., Borsboom, G. J. J. M.,
& Mackenbach, J. P. (2001). Neighborhood socioeconomic status and all-cause mortality. American Journal
of Epidemiology, 153, 363–371.
Centers for Disease Control and Prevention. (2017). National
Death Index [Data file]. Retrieved from http://www.cdc
.gov/nchs/ndi.htm
Chida, Y., & Steptoe, A. (2008). Positive psychological wellbeing and mortality: A quantitative review of prospective observational studies. Psychosomatic Medicine, 70,
741–756.
Chopik, W. J., & O’Brien, E. (2017). Happy you, healthy me?
Having a happy partner is independently associated with
better health in oneself. Health Psychology, 36, 21–30.
Diener, E., & Chan, M. Y. (2011). Happy people live longer:
Subjective well-being contributes to health and longevity. Applied Psychology: Health and Well-Being, 3, 1–43.
Diener, E., Emmons, R. A., Larsen, R. J., & Griffin, S. (1985).
The Satisfaction With Life Scale. Journal of Personality
Assessment, 49, 71–75.
Dyrenforth, P. S., Kashy, D. A., Donnellan, M. B., & Lucas,
R. E. (2010). Predicting relationship and life satisfaction
803
from personality in nationally representative samples
from three countries: The relative importance of actor,
partner, and similarity effects. Journal of Personality and
Social Psychology, 99, 690–702.
Jackson, S. E., Steptoe, A., & Wardle, J. (2015). The influence of partner’s behavior on health behavior change:
The English Longitudinal Study of Ageing. JAMA Internal
Medicine, 175, 385–392.
Jokela, M., Batty, G. D., Nyberg, S. T., Virtanen, M., Nabi, H.,
Singh-Manoux, A., & Kivimäki, M. (2013). Personality and
all-cause mortality: Individual-participant meta-analysis
of 3,947 deaths in 76,150 adults. American Journal of
Epidemiology, 178, 667–675.
Kim, E. S., Kubzansky, L. D., Soo, J., & Boehm, J. K. (2017).
Maintaining healthy behavior: A prospective study of
psychological well-being and physical activity. Annals
of Behavioral Medicine, 51, 337–347.
Lucas, R. (2005). Time does not heal all wounds: A longitudinal study of reaction and adaptation to divorce.
Psychological Science, 16, 945–950.
O’Malley, M. N., & Andrews, L. (1983). The effect of mood
and incentives on helping: Are there some things money
can’t buy? Motivation and Emotion, 7, 179–189.
Solomon, B. C., & Jackson, J. J. (2014). The long reach of
one’s spouse: Spouses’ personality influences occupational success. Psychological Science, 25, 2189–2198.
Therneau, T. M. (2015). A package for survival analysis in S
(Version 2.38) [Computer software]. Retrieved from
https://CRAN.R-project.org/package=survival
Uchino, B. N., Kent, R. G., Cronan, S., Smith, T. W., Diener, E.,
Joel, S., & Bosch, J. (2018). Life satisfaction and inflammation in couples: An actor–partner analysis. Journal of
Behavioral Medicine, 41, 22–30.
Weidmann, R., Schönbrodt, F. D., Ledermann, T., & Grob, A.
(2017). Concurrent and longitudinal dyadic polynomial
regression analyses of Big Five traits and relationship
satisfaction: Does similarity matter? Journal of Research
in Personality, 70, 6–15.
Zayas, V., Shoda, Y., & Ayduk, O. N. (2002). Personality in
context: An interpersonal systems perspective. Journal of
Personality, 70, 851–900.
Purchase answer to see full
attachment