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Running Head: SLEEP REHEARSAL OF EXTINCTION LEARNING 1
Having Therapy During Sleep?: Improving Extinction Learning for People with
Blood-Injection-Injury Fears by Rehearsing Memories During Sleep
Ki Eun Shin
Advisor: Richard E. Zinbarg
Second Reader: Ken A. Paller
I extend great thanks to Dr. Richard Zinbarg and Nehjla Mashal for their guidance and
support throughout all the stages of this process. I also thank Dr. Ken Paller.
This paper was supported by the Michael F. Dacey Research Grant from the Mathematical
Methods in the Social Sciences department of Northwestern University.
SLEEP REHEARSAL OF EXTINCTION LEARNING 2
Abstract
Patients often find exposure therapy aversive and sometimes have difficulty complying with
treatment. One method of addressing this problem is to enhance therapeutic learning by
capitalizing on memory consolidation during sleep. This study examined whether presenting
sounds associated with therapeutic information during sleep leads to greater symptom
reduction than exposure alone. Fourteen participants with blood-injection-injury fears
completed exposure and reflected on therapeutic lessons while listening to music. Half the
participants listened to the same music during their sleep for one week. Although not
significant, changes in participant ratings of anxiety and physical sensations in response to
fear-inducing stimuli were in the direction of superiority for the sleep rehearsal condition.
This suggests the possibility of augmenting exposure therapy with auditory-cued rehearsal of
therapeutic learning during sleep.
KEY WORDS: Exposure Therapy, Memory, Sleep, Blood-injection-injury Phobia
SLEEP REHEARSAL OF EXTINCTION LEARNING 3
Having Therapy During Sleep?: Improving Extinction Learning for People
with Blood-Injection-Injury Fears by Rehearsing Memories During Sleep
People find it difficult to face their fears although it is often the necessary first step to
be free of them. The dilemma becomes most prominent for a person with a phobia, an
excessive and irrational fear of an object or situation that poses little or no actual threat. A
common treatment for phobias, exposure therapy, requires patients to experience the feared
object or situation in a safe setting, without the feared negative outcome. Despite the
confirmed efficacy of exposure (Craske, Kircanski, Zelikowsky, Mystkowski, Chowdhury &
Baker, 2008; Norton & Price, 2007), patients with phobias often find the therapy process
aversive, and thus are reluctant to fully comply with treatment. The phenomenon leads to a
dilemma that people who want to be treated have difficulty facing therapy. In order to resolve
this dilemma, it is necessary to find ways to enhance treatment outcome without incurring
emotional burden on patients.
This paper reviews difficulties with patient compliance in exposure therapy and
explores possible avenues for enhancing therapy outcome. Exposure is conceptualized as a
form of inhibitory learning (Bouton, 2002; Craske et al., 2008), and potential methods of
augmenting exposure learning are introduced with an emphasis on sleep rehearsal of memory.
The present research is outlined, which investigates whether sleep rehearsal augments
exposure learning and improves treatment outcome for people with blood-injection-injury
(BII) fears.
Problems with Exposure Therapy
Exposure therapy is a common treatment for phobias and other anxiety disorders.
However, despite its wide use and confirmed efficacy (Craske et al., 2008; Norton & Price,
2007), patients tend to find the treatment difficult to tolerate. The distress of the exposure
process can hinder the efficacy of exposure-based therapy, creating problems before and
SLEEP REHEARSAL OF EXTINCTION LEARNING 4
during treatment. Even before the beginning of therapy, some patients choose to withdraw.
For instance, in a recent clinical trial for panic disorder, 5% of patients dropped out before
treatment (White, Allen, Barlow, Gorman, Shear, & Woods, 2010). Similarly, in an exposure-
based protocol for obsessive-compulsive disorder (OCD), pretreatment dropout was 6%,
(Whittal, Thordarson, & McLean, 2005). In an outpatient treatment for anxiety disorders, the
refusal rate reached 30.4% (Issakidis & Andrews, 2004).
Patients who decide to initiate therapy also may not complete the treatment. A
sizeable fraction of individuals with anxiety disorders do not remain in treatment (Huppert &
Baker-Morissette, 2003; Issakidis & Andrews, 2004; Leahy, 2001; Westen & Morrison,
2001). In an outpatient treatment for anxiety disorders, the dropout rate was 10.3% (Issakidis
& Andrews, 2004). Similarly, 14.5% of OCD patients (Whittal et al. (2005) and 15.6% of
patients with panic disorder (Öst, Thulin, & Ramnero, 2004) prematurely terminated their
treatment in an exposure-based cognitive behavioral therapy. In a clinical trial for panic
disorder, the patient dropout rate was 19%, and patients dropped out most frequently after
treatment sessions entailing exposure (White et al., 2010). A meta-analysis of cognitive-
behavioral treatment for social phobia shows that an average of 16.4% (SD = 7.4, across 8
studies) of patients receiving exposure therapy dropped out (Taylor, 1996).
In addition, patient compliance rates among those who remain in therapy tend to be
low in exposure therapy (Abramowitz, Franklin, Zoellner, & DiBernardo, 2002; Foa et al.,
1983; Scott & Stradling, 1997; Simpson, Huppert, Petkova, Foa, & Liebowitz, 2006). In a
clinical trial for posttraumatic stress disorder (PTSD), only 57% of participants followed the
therapist’s directions for daily exposure homework (Scott & Strandling, 1997). Participant
compliance matters because it affects treatment response (Issakidis & Andrews, 2004). Better
compliance predicts greater improvement in post-treatment functioning (Mischelson,
Mavissakalian, Marchione, Dancu, & Greenwalk, 1986) and long-term maintenance of
SLEEP REHEARSAL OF EXTINCTION LEARNING 5
treatment gains (Park, Mataix-Cols, Marks, Ngamthipwatthana, Marks, Araya, & Al Rescorla,
2001). On the other hand, low compliance can lead to suboptimal therapy outcome despite
completion of treatment (Sanderson & Bruce, 2007).
Enhancing Exposure Therapy
Exposure therapy has been widely conceptualized as a form of inhibitory learning
(Bouton, 2002; Craske et al., 2008). Phobias are considered to be often a product of fear
conditioning in which an individual develops a negative association for an object or situation
and becomes fearful of related stimuli (Bouton, 2002; Craske et al., 2008). Exposure therapy
may alleviate fears by inducing new inhibitory learning rather than deleting or weakening
previous excitatory (fearful) learning (Bouton, Woods, & Pineno, 2004; Rescorla, 2001). The
fearful association remains intact, but the newly learned safety association competes with the
old fear learning (Bouton, 2002). Successful exposure treatment occurs when the new
association becomes a dominant response to the once fear-inducing stimuli. The
establishment of new safety association is called extinction.
Based on the learning mechanism of extinction, previous attempts to enhance
exposure therapy focused on memory consolidation and retrieval of inhibitory learning
(Craske et al, 2008). One line of research examined effects of varying phobic stimuli and
spaced scheduling of exposure sessions on treatment outcome. Varying phobic stimuli in
exposure sessions helps patients remember the learned information better because it provides
multiple memory cues instead of a single cue (Bjork, 1988; Bjork & Bjork, 1992; Magill &
Hall, 1990). For instance, one study showed that exposure to varied phobic stimuli (i.e.,
multiple spiders) led to better maintenance of treatment gains at follow-up than did exposure
to the same stimulus (i.e., a single spider) (Rowe & Craske, 1998).
Another method is to space out exposure sessions over a longer time period rather
than to cluster them over a short time period. Spaced learning trials improve retrieval of
SLEEP REHEARSAL OF EXTINCTION LEARNING 6
learned information (Fanselow, DeCola, & Young, 1993; Josselyn et al., 2001; Kogan et al.,
1997; Scharf et al., 2002) possibly because partial forgetting between the learning trials leads
to greater storage strength of the memory (Bjork & Bjork, 1992). For instance, spaced
exposure (20 minutes on 4 days) produced better treatment response than massed exposure
(40 minutes on 2 days) for specific phobia (Ramsay, Barenda, Breuker, & Kruseman, 1966).
However, there are also discrepant findings. In another study (Foa, Jameson, Turner, & Payne,
1980), massed (daily) rather than spaced (weekly) exposure sessions led to greater symptom
reduction in individuals with agoraphobia. Many other studies did not find a significant
difference between massed and spaced exposure schedules (Berah, 1981; Chambless, 1990;
Ning & Liddell, 1991).
Supplementing exposure therapy with a biochemical substance such as D-cycloserine
(DCS) has been also explored. DCS has been shown to enhance consolidation of extinction
learning in both animals (Richardson, Ledgerwood, & Cranney, 2004; Santini, Muller, &
Quirk, 2001; Woods & Bouton, 2006; Davis, 2002) and humans (Ressler et al., 2004; Davis,
Ressler, Rothbaum, & Richardson, 2006). The use of DCS in exposure therapy led to better
maintenance of treatment gains at both post-treatment and follow-up compared with a
placebo condition (Norberg, Krystal, & Tolin, 2008). Other biological agents such as
yohimbine and glucocorticoid cortisone also improved treatment outcome in claustrophobia
and social phobia respectively (Powers, Smits, Otto, et al., 2009; Soravia, Heinrich, Aerni, et
al., 2006). However, despite the initial promising results, the effect of DCS does not always
appear significant (Guastella, Dadds, Lovibond, Mitchell, & Richardson, 2007). Thus, further
evaluation is necessary to elucidate the role of DCS in extinction learning.
Sleep, Memory, and Extinction
The literature on sleep and memory suggests another way to enhance extinction
learning. Previous studies showed that sleep aids in encoding and consolidation of new
SLEEP REHEARSAL OF EXTINCTION LEARNING 7
memories (especially emotional memories; Walker, & van der Helm, 2009) and may
facilitate integration of new memories with old ones (Diekelmann & Born, 2010; Walker &
Stickgold, 2010). Researchers have also demonstrated that sleep generalizes the extinction
response to novel phobic stimuli not specifically targeted in an exposure session (Pace-Schott
et al., 2009). In this study, participants were conditioned to fear two differently colored lamps
using mild electric shocks. Experimenters extinguished participants’ fear response to one of
the lamps by repeatedly presenting the lamp without shocks. Later, the fear conditioning was
measured by skin conductance response, and participants who slept for twelve hours showed
decreased fear response to both the extinguished and unextinguished stimuli whereas those
who stayed awake for twelve hours showed decreased fear response only to the extinguished
stimulus.
A recent study provides an insight on how to apply enhancing memory consolidation
during sleep to exposure therapy (Rudoy, Voss, Westerberg, & Paller, 2009). In this study,
participants saw 50 images, individually appearing on different parts of a computer screen
and memorized the images’ locations. When an image appeared on a screen, a related sound
was played (e.g. cat-meow). Later, participants took a nap, and their brainwaves were
measured by EEG equipments. During slow wave sleep, half of the 50 different sounds were
replayed. The result showed better recall of the images cued by related sounds during sleep
than those not cued during sleep.
Similar methodology can be applied to exposure therapy. If cued sleep enhances
extinction learning as it did for spatial memory learning, it would have meaningful clinical
applications. For instance, the number of exposure sessions necessary to achieve symptom
reduction might decrease because a part of the work can be done during sleep outside
sessions. As the sleep rehearsal would cause less emotional distress than actual exposure
sessions, previously reluctant patients might be more willing to initiate, engage in, and
SLEEP REHEARSAL OF EXTINCTION LEARNING 8
remain in therapy. Noncompliant patients may still be able to achieve desirable treatment
outcomes with reinforced learning during sleep. Furthermore, continued use of auditory
enhancement during sleep might help patients to maintain treatment gains for a longer time
period, preventing early relapse.
A previous study (Panton, 2011) examined effects of sleep rehearsal on treatment
outcome of exposure therapy for blood-injection-injury (BII) phobia. BII phobia refers to an
intense fear and avoidance of blood and blood-related items or events such as needles,
injections, injuries, and surgeries (Sarlo et al, 2008). In this study, participants with BII fears
completed an exposure session and after the session, listened to a music clip while reviewing
the exposure learning. Participants in the sleep rehearsal condition were instructed to listen to
the same music clip during their sleep at each night for one week. The study compared
degrees of symptom reduction in the sleep rehearsal condition and the control condition.
The result showed a trend in the direction of superiority for the sleep rehearsal
condition to the control condition, but the difference was not significant (Panton, 2011). Two
limitations of the study may account for the non-significant result. Participants were from the
Introduction to Psychology student pool, who participated to fulfill their class requirement.
Because they did not voluntarily choose to participate in the study, participants might have
had little motivation to complete the daily assignments for sleep rehearsal. In addition, the
study solely relied on participants’ self-reports for a manipulation check, thus lacking other
objective measures to test the reports’ accuracy.
The Present Research
The current study aimed to replicate the previous research by Panton (2011) and
explore whether adding sounds presented during encoding of therapeutic information and
later presented during sleep leads to greater symptom reduction than exposure alone. The
current study focused on exposure therapy for BII phobia for two practical reasons: 1) BII
SLEEP REHEARSAL OF EXTINCTION LEARNING 9
phobia can be effectively treated by one exposure session of three to five hours (Öst, 1989),
and 2) the phobic stimuli to be used in sessions are more readily available for BII phobia than
for other phobias (e.g. images of blood vs. housing a spider). The goal of the current study
was to address limitations of the previous study (Panton, 2011). Improvements from the
previous study included participant recruitment from community samples instead of
Introduction to Psychology student pool and addition of a manipulation check (the play
counts in an MP3 player). In addition, the previous music clip was modified to have more
positive valence, and white noise was inserted at the beginning of the clip for sleep rehearsal
to facilitate sleep.
Method
Participants
Fourteen participants (5 male, 9 female) were recruited in the Northern Chicagoland
area via online advertisements, newspaper advertisements, and posted flyers. Participants
were pre-selected based on a 15-minute structured clinical interview to determine whether
they met the DSM-IV-TR criteria for specific phobia, Blood-Injection-Injury (BII) Type.
Block randomization was used to pair up participants and assign half the pairs to the sleep
rehearsal condition, and the other half to the control condition. The age of participants ranged
from 18 to 73 years (M = 32.1, SD = 14.5). Eighty percent of participants identified
themselves as Caucasian, 13% East Asian, and 7% African American. All participants
received $20.00 compensation at the end of the study.
Materials
Diagnostic Interview. To determine eligibility for this study, a graduate student
trained in administration of the Structured Clinical Interview for DSM-IV-TR Axis I
Disorders (SCID I; First, Spitzer, Gibbon, & Williams, 2002) interviewed potential
participants. The interview included the specific phobia section of the SCID, which indicated
SLEEP REHEARSAL OF EXTINCTION LEARNING 10
whether participants met the DSM-IV TR criteria for specific phobia, Blood-Injection-Injury
(BII) Type. The criteria include excessive and persistent fear of BII related situations (e.g.
surgery, venipuncture) and anxiety upon encountering such situations. The person either
avoids the situations or endures them with considerable distress. He or she also perceives the
fear as irrational or excessive, and the fear and avoidance cause functional impairment (e.g.
reluctance to receive necessary medical care).
Self-report Measures of BII Fear. Participants filled out three questionnaires in the
pre and the post session: The Mutilation Questionnaire (MQ), the Blood-Injection Symptom
Scale (BISS), and nine items from the Fear Survey Schedule (FSS). The MQ (Klorman,
Weerts, Hastings, Melamed, & Lang, 1974) is a 30 true/false item questionnaire that
measures the verbal/cognitive component of mutilation and BII fear (e.g. “I dislike looking at
pictures of accidents or injuries in magazines”). The MQ has been used as a predictor of BII
phobia and fainting (Kleinknecht, & Thorndike, 1990; Oliver & Page, 2008). The BISS (Page,
Bennett, Carter, Smith, & Woodmore, 1997) is a 17 item yes/no questionnaire measuring
phobic symptoms experienced in situations involving blood or injections (e.g. “Were you
dizzy or lightheaded?”). The nine items from the FSS (Wolpe & Lang, 1974) measure
fearfulness for BII-related stimuli (e.g. “Open Wounds,” “Receiving Injections”) on a 7-point
scale (0 = None, 3 = Some fear, 6 = Terror).
Behavioral Avoidance Task (BAT). A 10-minute behavioral avoidance task (BAT)
was used in the pre and the post session to measure levels of fear and anxiety. In the BAT,
participants saw each of the 12 pictures related to BII fears on a computer screen (e.g. a
picture of a syringe or open wounds). The task began with the least fear-inducing image, and
at each step, images became progressively more fear-inducing. Throughout the task,
participants proceeded at their own pace. When participants felt uncomfortable or unwilling
to continue, they could exit the BAT. Fear was measured by the number of steps participants
SLEEP REHEARSAL OF EXTINCTION LEARNING 11
made during the BAT. A greater number of completed steps meant a lower level of BII fears.
The BAT paradigm has been successfully used in other studies on specific phobia (Oliver &
Page, 2008; Tsao & McKay, 2004) to compare the pre- and the post-treatment levels of fear.
During the BAT, participants’ looking time was measured to examine gaze aversion.
Exposure to fear-related stimuli in individuals with phobias leads to visual avoidance (Tolin,
Lohr, Lee, & Sawchuk, 1999). The looking time was measured via each participant’s reaction
time during the BAT, aggregated across the 12 pictures. The longer looking time indicated
less visual avoidance.
Subjective Units of Distress Scale (SUDS) & Physiological Rating. During the
BAT and the exposure tasks, a Subjective Units of Distress Scale (SUDS; Wolpe, 1969) and
a 10-point scale for physiological sensations were used to measure within- and between-
session changes in fear reduction. After viewing each picture in the BAT and completing an
exposure task, participants rated their level of distress on a SUDS from 0 (no fear) to 10
(highest fear) and also rated the intensity of physiological sensations (e.g. nausea or light-
headedness) on a scale from 0 to 10. The SUDS rating indicates the subjective level of
distress experienced by an individual (Wolpe, 1969). The scale has been used to evaluate
treatment progress in studies on posttraumatic stress disorder, obsessive-compulsive disorder,
and specific phobia (Devilly & Spence, 1999; Oliver & Page, 2008; Taylor, 1998).
Procedure
This study included the pre and the post sessions, administered a week apart. To have
an equal number of participants in each condition, block randomization was used.
Experimenters paired up participants and randomly assigned one person from each pair to the
sleep rehearsal condition, and the other, to the control condition.
Pre Session. Participants came to the lab and first filled out the informed consent
forms. Participants also filled out a questionnaire packet including the MQ, the BISS, and the
SLEEP REHEARSAL OF EXTINCTION LEARNING 12
FSS. The experimenter provided brief explanation about BII phobia and exposure therapy
and introduced the Behavioral Avoidance Task. For the next ten minutes, participants
completed the BAT, viewing 12 BII-related images and rating their level of distress and
physiological sensations on the SUDS and the 10-point physiological sensation scale.
Throughout the BAT, participants’ faces were video recorded using a 9000 Logitech camera.
Participants then moved to another room and began the exposure session. The
exposure session consisted of four tasks in the order of the least to the most anxiety-
provoking. The first task involved watching three brief videos of blood and surgery. The task
continued until participants felt comfortable watching the most fear-inducing video. The
second task was holding a bag of stage blood for as long as participants felt comfortable. In
the third task, participants watched a set of needles while the experimenter held them in her
hand, and they also held the needles themselves. The last task involved watching the
experimenter prick herself with a sterile mini lancet. Participants who were willing also
pricked themselves with a lancet. After each task, participants rated their level of distress and
physiological sensations on the SUDS and the physiological sensation scale. Throughout the
exposure session, participants proceeded at their own pace and could stop at any point they
felt uncomfortable. The entire exposure session took approximately 40 minutes.
After the exposure session, participants reflected on the exposure tasks for 10
minutes. The experimenter guided them by going over each task and benefits of the exposure
experience. During the reflection period, participants listened to a music clip in the
background. The music was a novel piece created for the use in this study and had neutral to
positive valence. After the reflection period, participants in the control condition left, and
those in the sleep rehearsal condition received instructions for sleep rehearsal. The
experimenter gave them a sleep record sheet and an MP3 player with a music clip. The clip
SLEEP REHEARSAL OF EXTINCTION LEARNING 13
included white noise for the first 30 minutes, and the rest was 6 hours of the same music
participants listened to during the reflection period.
Sleep Rehearsal. For one week after the pre session, participants in the sleep
rehearsal condition were instructed to listen to the clip during their sleep at each night. They
recorded on the sleep record sheet the time they went to sleep and woke up and the hours they
listened to the clip. The self reports were later compared with the music play counts
automatically stored in the MP3 player distributed to participants.
Post Session. After one week from the pre session, participants visited the lab again.
For the sleep rehearsal condition, the experimenter retrieved the MP3 player and the sleep
record sheet. As in the pre session, participants filled out a questionnaire packet of the MQ,
the BISS, and the FSS. Participants also completed the second BAT with the same 12 images
used in the first BAT and provided the SUDS and physiological sensation ratings. After the
BAT, the experimenter verbally debriefed participants and answered if they had any question.
Results
Manipulation Check
Participant self-reports and MP3 player play counts were used as a manipulation
check. Seven participants in the sleep rehearsal condition recorded on the sleep record sheet
duration of their sleep and the number of hours they listened to the clip each night. MP3
player play counts were used to measure how many times each participant listened to the
music clip. Due to a technical failure, the play counts were only collected from four
participants in the sleep rehearsal condition.
According to self-reports, participants in the sleep rehearsal condition listened to the
music clip for 25.4 hours on average (SD = 22.4). See Figure 1 for the distribution of self-
reported listening hours. For the four participants from whom both measures were collected,
there was a discrepancy between self-reports and play counts (see Figure 2). According to
SLEEP REHEARSAL OF EXTINCTION LEARNING 14
self-reports, the participants listened to the music clip for 19.6 hours on average (SD = 21.6).
According to play counts, they listened to it for 13.7 hours on average (SD = 21.5). Based on
self-reports and play counts, three participants in the sleep rehearsal condition listened to the
clip for less than three hours. Because the three participants clearly did not receive the
manipulation as intended, their data was excluded from analysis.
Subjective Distress Rating & Physiological Rating.
We predicted that the sleep rehearsal condition would show a greater pre to post
decrease in subjective distress and physiological ratings than controls. Independent samples t-
tests with an alpha level of .05 did not reveal a significant effect of group for the pre to post
changes in subjective distress and physiological ratings. However, the group difference was
in the direction of superiority for the sleep rehearsal condition, t(9) = -.98, p = .35, d = .67
and t(9) = -1.59, p = .15, d = 1.01, respectively. Whereas participants in the control condition
showed a mean decrease of .71 in subjective distress ratings (SD = 1.55) and of -.07 in
physiological ratings (SD = 1.43), participants in the sleep rehearsal condition showed a mean
decrease of 1.75 in subjective distress ratings (SD = 1.94) and of 1.38 in physiological ratings
(SD = 1.49).
Looking Time & Self-report Questionnaires
We predicted that the sleep rehearsal condition would also show a greater pre to post
increase in looking time and a greater pre to post decrease in self-report measures of BII fears
than controls. Independent samples t-tests with an alpha level of .05 did not reveal significant
differences between the control and the sleep rehearsal condition. Participants in the control
condition showed a mean decrease of 1936.64 in looking time (SD = 6755.30), and
participants in the sleep rehearsal condition showed a mean decrease of 3603.50 in looking
time (SD = 6491.30), t(9) = .40, p = .70, d = .25. Participants in the control condition also
showed a mean decrease of .49 in the Fear Survey Schedule scores (SD = .70) and a mean
SLEEP REHEARSAL OF EXTINCTION LEARNING 15
increase of .01 in the Blood-Injection Symptom Scale scores (SD = .09) whereas participants
in the sleep rehearsal condition showed a mean decrease of .64 in the FSS scores (SD = 1.17)
and a mean increase of .03 in the BISS scores (SD = .25), t(9) = -.28, p = .79, d = .21 and t(9)
= .17, p = .87, d = .22, respectively. However, results concerning the Mutilation
Questionnaire were in the direction of superiority for the sleep rehearsal condition, t(9) = -
1.66, p = .13, d = 1.67. While participants in the control condition had a mean decrease of .05
(SD = .09), participants in the sleep rehearsal condition had a mean decrease of .20 in MQ
scores (SD = .22).
Discussion
The present study aimed to investigate whether the addition of music presented
during encoding of therapeutic information and later, during sleep, enhances the outcome of
exposure. Results failed to support that exposure with auditory-cued sleep rehearsal leads to
superior treatment outcomes compared to exposure alone. However, because of the low
participant compliance and restricted sample size, the current study did not provide an
adequate test of the hypotheses. The lack of an effect might be due to insufficient
manipulation of the variable of interest and/or low statistical power. Given that results were
generally in the direction of superiority for the sleep rehearsal condition, a future study with a
larger sample size and better implementation of the manipulation is warranted.
Another limitation of this study involves lack of facial coding data. Participants’ faces
were video-recorded to examine gaze aversion and facial disgust during Behavioral
Avoidance Task, but the data could not be included in this report as the coding is not yet
complete. In the current study, looking time was measured via reaction times during
Behavioral Avoidance Task. However, individuals with phobias tend to avert their eyes from
fear-inducing stimuli (Tolin et al., 1999), and therefore, it is necessary to record duration of
visual avoidance during BAT and adjust the reaction time to obtain a more accurate measure
SLEEP REHEARSAL OF EXTINCTION LEARNING 16
of looking time. In addition, previous studies showed that disgust, rather than fear, is a
dominant response of people with BII fears during pictorial exposure to blood and bodily
injury (Olantunji, Lohr, Sawchuk, & Patten, 2007). Thus, facial coding of participants’
disgust reactions during BAT would have been a useful measure of pre-to-post symptom
reduction in addition to subjective distress and physiological ratings.
One of the goals of the current study was to improve on a past study (Panton, 2011)
by addressing the problem of low participant compliance by recruiting from a different pool
of subjects. In the previous study (Panton, 2011), participants were recruited from the
Introduction to Psychology student pool, who participated to satisfy research participation
requirements for the class. In the current study, participants were recruited from the
community to better ensure that participants were interested in reducing their fears and
motivated to listen to the clip during sleep each night for a week. However, recruiting from
the community instead of the Introduction to Psychology student pool did not lead to greater
participant compliance. According to participant self-reports, the participants in the sleep
rehearsal condition listened to the clip for 3.6 hours per day on average. Three participants in
the sleep rehearsal condition listened to the clip for less than three hours during a week. As a
result of low participant compliance, the study failed to provide an adequate test of whether
listening to sounds associated with therapeutic information during sleep leads to greater
symptom reduction than exposure alone.
Different factors may account for the low participant compliance in the current study.
First, some participants might not have been interested in reducing their fears and therefore
were not motivated enough to comply with the experimental protocol. When asked during the
post session, several participants answered that their primary reason for participating was
monetary compensation rather than overcoming their fears. Alternatively, participants might
have found it uncomfortable to listen to the clip during sleep or had difficulty falling asleep
SLEEP REHEARSAL OF EXTINCTION LEARNING 17
because of the sounds. In addition, participants could have associated the music clip with
aversive experiences of exposure and were thus reluctant to listen to it during sleep. In the pre
session, participants completed exposure tasks and had a reflection period to review positive
therapeutic gains from the tasks while simultaneously listening to a music clip. The purpose
of the reflection period was to establish an association between therapeutic learning and the
music clip. However, reflecting on therapeutic gains might have reminded participants of
their anxiety during the exposure tasks, resulting in an association between the music clip and
anxiety as well as therapeutic learning. Given that emotional salience enhances memory
(Parent et al., 2011), strong emotions such as fear or disgust could have been paired more
strongly with the clip than therapeutic learning. As a result, participants might have been
reluctant to listen to the clip because it reminded them of aversive experiences of exposure.
Depending on its potential cause, the low participant compliance of this study has
different implications for the use of auditory-cued sleep rehearsal in a therapeutic setting. If
the reason for the low compliance is lack of motivation in participants, there is a potential for
better compliance in a therapeutic setting. Patients participating in actual therapy are
treatment-seekers who are motivated to overcome their fears and thus, are likely to comply
with the instruction better. On the other hand, if the low compliance is due to discomfort
during auditory-cued sleep rehearsal or the music clip’s evocation of anxiety, patients are less
likely to show improved compliance in a therapeutic setting. If patients find the experience of
auditory-cued sleep rehearsal uncomfortable or anxiety-provoking, despite their desire to
overcome fears, they might not be willing to comply with the intervention. These possibilities
raise questions about feasibility of implementing auditory-cued sleep rehearsal in a
therapeutic setting. Although the current study lacked a sufficient sample size to confirm
whether auditory-cued sleep rehearsal is effective, the low compliance rate casts doubt on
whether auditory-cued sleep rehearsal is a practical method of augmenting exposure therapy.
SLEEP REHEARSAL OF EXTINCTION LEARNING 18
Despite the possibly limited therapeutic application, however, a future study on
auditory-cued sleep rehearsal of therapeutic learning would still be valuable. It can contribute
to the understanding of the relationship between extinction learning (exposure) and memory
consolidation during sleep. In conducting such a study, it is necessary to address limitations
of the current study by using a larger sample and changing the experimental protocol to
ensure that manipulation is delivered. One way to implement the manipulation, independent
of participant motivation for compliance on their own would be bringing in participants to a
lab to take a nap (e.g. Lau, Alger, & Fishbein, 2011; Spoormaker et al., 2010).
If a larger sample size and successful implementation of manipulation leads to an
enhancement effect, the result would replicate previous findings that sleep plays a role in
memory consolidation of extinction learning (Pace-Schott et al., 2009; Spoormaker et al.,
2010). The result would also illuminate the application of the auditory-cued sleep rehearsal
paradigm to different kinds of learning other than spatial memory learning (Rudoy et al.,
2009).
Overall, the results of the present study failed to support the hypothesis that listening
to sounds associated with therapeutic learning leads to greater symptom reduction than
exposure alone. However, due to limitations of the study, including low participant
compliance and small sample size, the current study did not provide an adequate test of this
hypothesis. Given that some of the results were in the direction of superiority for the sleep
rehearsal condition, future research should be conducted to confirm the effectiveness of
auditory-cued sleep rehearsal, with a larger sample size and more effective implementation of
the manipulation. In addition, the low participant compliance in a past study (Panton, 2011)
and the current study suggests that auditory-cued sleep rehearsal needs to be carefully
thought through before it could be a viable method of augmenting exposure therapy.
SLEEP REHEARSAL OF EXTINCTION LEARNING 19
References
Abramowitz, J. S., Franklin, M. E., Zoellner, L. A., & DiBernardo, C. L. (2002). Treatment
compliance and outcome in obsessive-compulsive disorder. Behavior Modification,
26(4), 447-463.
Berah, E. F. (1981). Influence of scheduling variations on the effectiveness of a group
assertion-training program for women. Journal of Counseling Psychology, 28(3),
265–268.
Bjork, R. A. (1988). Retrieval practice and the maintenance of knowledge. In M. M.
Gruneberg, P. E. Morris, & R. N. Sykes (Eds.), Practical aspects of memory:
Current research and issues: Memory in everyday life, Vol. 1 (pp. 196–401). Oxford,
England: Wiley.
Bjork, R. A., & Bjork, E. L. (1992). A new theory of disuse and an old theory of stimulus
fluctuation. In A. Healy, S. Kosslyn, & R. Shiffrin (Eds.), From learning processes
to cognitive processes: Essays in honor of William K. Estes (pp. 35–67). Hillsdale,
NJ: Erlbaum.
Bouton, M. E. (2002). Context, ambiguity, and unlearning: Sources of relapse after
behavioral extinction. Biological Psychiatry, 52(10), 976-986.
Bouton, M. E., Woods, A. M., & Pineño, O. (2004). Occasional reinforced trials during
extinction can slow the rate of rapid reacquisition. Learning and Motivation, 35(4),
371-390.
Chambless, D. L. (1990). Spacing of exposure sessions in treatment of agoraphobia and
simple phobia. Behavior Therapy, 21, 217–229.
Craske, M.G., Kircanski, K., Zelikowsky, M., Mystkowski, J., Chowdhury, N., & Baker, A.
(2008). Optimizing inhibitory learning during exposure therapy. Behaviour Research
SLEEP REHEARSAL OF EXTINCTION LEARNING 20
and Therapy, 46, 5–27
Davis, M., Ressler, K., Rothbaum, B. O., & Richardson, R. (2006). Effects of D-cycloserine
on extinction: Translation from preclinical to clinical work. Biological Psychiatry,
60(4), 369-375.
Devilly, G. J. & Spence, S. H. (1999). The relative efficacy and treatment distress of EMDR
and a cognitive behavior trauma treatment protocol in the amelioration of post
traumatic stress disorder, Journal of Anxiety Disorders, 13, 131-157.
Foa, E. B., Grayson, J. B., Steketee, G. S., Doppelt, H. G., Turner, R. M., & Latimer, P. R.
(1983). Success and failure in the behavioral treatment of obsessive-compulsives.
Journal of Consulting and Clinical Psychology, 51(2), 287-297.
Foa, E. B., Jameson, J. S., Turner, R. M., & Payne, L. L. (1980). Massed vs. spaced exposure
sessions in the treatment of agoraphobia. Behaviour Research and Therapy, 18(4),
333–338.
Guastella, A. J., Dadds, M. R., Lovibond, P. F., Mitchell, P., & Richardson, R. (2007). A
randomized controlled trial of the effect of D-cycloserine on exposure therapy for
spider fear. Journal of Psychiatric Research, 41(6), 466–471.
Guastella, A.J., Richardson, R., Lovibond, P.F., Rapee, R.M., Gaton, J.E., Mitchell, P., &
Dadds, M.R. (2008). A randomized controlled trial of D-cycloserine enhancement of
exposure therapy for social anxiety disorder, Biological Psychiatry, 63(6), 544-549.
Hofmann, S.G., Meuret A. E., Smits, J., Simon, N. M., Pollack, M. H., Eisenmenger, K.,
Shiekh, M., & Otto, M.W. (2006). Augmentation of exposure therapy with D-
cycloserine for social anxiety disorder. Archives of General Psychiatry, 62, 298-304.
Huppert, J. D., & Baker-Morrisette, S. L. (2003). Beyond the manual: The insider's guide to
panic control treatment. Cognitive and Behavioral Practice, 10(1), 2-13.
SLEEP REHEARSAL OF EXTINCTION LEARNING 21
Issakidis, C., & Andrews, G. G. (2004). Pretreatment attrition and dropout in an outpatient
clinic for anxiety disorders. Acta Psychiatrica Scandinavica, 109(6), 426-433.
Kushner, M.G., Kim S.W., Donahue C., Thuras, P., Adson, D., Kotlyar, M., McCabe, J.,
Peterson, J., & Foa, (2007). D-Cycloserine augmented exposure therapy for
obsessive-compulsive disorder. Biological Psychiatry, 62(8), 835-838.
Lau, H., Alger, S.E., & Fishbein, W. (2011). Relational memory: A daytime nap facilitates
the abstraction of general concepts. PLoS ONE, 6(11), doi:
10.1371/journal.pone.0027139
McDonald, R., Marks, I.,& Blizard, R. (1988). Quality assurance in mental health care: A
model for routineusein clinical settings. Health Trends, 20, 111-114.
Michelson, L., Mavissakalian, M., Marchione, K., Dancu, C., & Greenwald, M. (1986). The
role of self directed in vivo exposure in cognitive, behavioral, and
psychophysiological treatments of agoraphobia. Behavior Therapy, 17, 91–108.
Ning, L., & Liddell, A. (1991). The effect of concordance in the treatment of clients with
dental anxiety. Behavior Research and Therapy, 29(4), 315–322.
Norberg, M.M., Krystal, J.H., & Tolin, D.F. (2008). A meta-analysis of D-cycloserine and
the facilitation of fear extinction and exposure therapy. Biological Psychiatry, 63,
1118-1126.
Norton, P. J., & Price, E. C. (2007). A meta-analytic review of adult cognitive-behavioral
treatment outcome across anxiety disorders. Journal of Nervous and Mental Disease,
195(6), 521–531.
Olatunji, B.O., Lohr, J.M., Sawchuk, C. N.,&Patten,K. (2007). Fear and disgust responding
to heterogeneous blood-injection-injury stimuli: Distinctions from anxiety symptoms.
Journal of Psychopathology and Behavioral Assessment, 29, 1–8
Öst, L. (1989). One-session treatment for specific phobias. Behaviour Research and Therapy,
SLEEP REHEARSAL OF EXTINCTION LEARNING 22
27(1), 1-7.
Pace-Schott, E. F., Milad, M. R., Orr, S. P., Rauch, S. L., Stickgold, R., & Pitman, R. K.
(2009). Sleep promotes generalization of extinction of conditioned fear. Sleep, 32(1),
19–26.
Panton, Christina (2011). Improving Therapy Outcomes by Enhancing Learning During
Sleep (Unpublished undergraduate honors thesis). Northwestern University,
Evanston, IL.
Parent, M.B., Krebs-Kraft, D. L., Ryan, J.P., Wilson, J.S., Harenski, C., & Hamann, S. (2011).
Glucose administration enhances fMRI brain activation and connectivity related to
episodic memory encoding for neutral and emotional stimuli. Neuropsychologia,
49(5), 1052-1066.
Park, J., Mataix-Cols, D., Marks, I. M., Ngamthipwatthana, T., Marks, M., Araya, R., & Al
Rescorla, R. A. (2001). Experimental extinction. In R. R. Mowrer, S. B. Klein (Eds.),
Handbook of contemporary learning theories (pp. 119-154). Mahwah, NJ US:
Lawrence Erlbaum Associates Publishers.
Ressler, K. J., Rothbaum, B. O., Tannenbaum, L., Anderson, P., Graap, K., Zimand, E., &
Davis, M. (2004). Cognitive enhancers as adjuncts to psychotherapy: Use of D-
cycloserine in phobic individuals to facilitate extinction of fear. Archives of
General Psychiatry, 61(11), 1136-1144.
Rowe, M. K., & Craske, M. G. (1998). Effects of varied-stimulus exposure training on fear
reduction and return of fear. Behavior Research and Therapy, 36, 719-734.
Rudoy, J. D., Voss, J. L., Westerberg, C. E., & Paller, K. A. (2009). Strengthening individual
memories by reactivating them during sleep. Science, 326, 1079.
SLEEP REHEARSAL OF EXTINCTION LEARNING 23
Sanderson, W. C., & Bruce, T. J. (2007). Causes and management of treatment-resistant
panic disorder and agoraphobia: A survey of expert therapists. Cognitive and
Behavioral Practice, 14(1), 26-35.
Sarlo, M., Buodo, G., Munafò, M., Stegagno, L., & Palomba, D. (2008).
Cardiovasculardynamics in blood phobia: Evidence for a key role of sympathetic
activity in vulnerability to syncope. Psychophysiology, 45(6), 1038-1045.
Scott, M. X. & Stradling, S. G. (1997). Client compliance with exposure treatments for
posttraumatic stress disorder. Journal of Traumatic Stress, 10(3), 523-526.
Simpson, H. B., Huppert, J. D., Petkova, E., Foa, E. B., & Liebowitz, M. R. (2006).
Response versus remission in obsessive-compulsive disorder. Journal of Clinical
Psychiatry, 67(2), 269-276.
Soravia, L.M., Heinrichs, M., Aerni, A., Maroni, C., Schelling, G., Ehlert, U., Roozendaals,
B., de Quervain, D. (2006). Glucocorticoids reduce phobic fear in humans.
Proceedings of the National Academy of Sciences of the United States of America,
103(14), 5585-5590.
Spoormaker, V. I., Sturm, A., Andrade, K.C., Schroter, M.S., Goya-Maldonado, R., Holsboer,
F., Wetter, T.C., Samann, P.G., & Czisch, M. (2010). The neural correlates and
temporal sequence of the relationship between shock exposure, disturbed sleep and
impaired consolidation of fear extinction. Journal of Psychiatric Research, 44(16),
1121-1128.
Taylor, S. (1998). Assessment of Obsessive-compulsive Disorder. In R. P. Swinson, M. M.
Antony, S. Rachman & M. A. Richter, (Eds.), Obsessive-compulsive disorder:
Theory, research, and treatment (pp. 229-257). New York, NY: The Guilford Press.
Taylor, S. (1996). Meta-analysis of cognitive-behavioral treatment for social phobia. Journal
of Behavior Therapy and Experimental Psychiatry, 27(1), 1-9.
SLEEP REHEARSAL OF EXTINCTION LEARNING 24
Tolin, D. F., Lohr, J. M., Lee, T. C., & Sawchuk, C. N. (1999). Visual avoidance in specific
phobia. Behavioral Research and Therapy, 37, 63-70.
Tsao, S. D. & McKay, D. (2004). Behavioral avoidance tests and disgust in contamination
fears: distinctions from trait anxiety. Behavioral Research and Therapy, 42, 207-216.
Westen, D., & Morrison, K. (2001). A multidimensional meta-analysis of treatments for
depression, panic, and generalized anxiety disorder: An empirical examination of the
status of empirically supported therapies. Journal of Consulting and Clinical
Psychology, 69(6), 875-899.
White, K. S., Allen, L. B., Barlow, D. H., Gorman, J. M., Shear, M., & Woods, S. W. (2010).
Attrition in a multicenter clinical trial for panic disorder. Journal of Nervous and
Mental Disease, 198(9), 665-671.
Whittal, M. L., Thordarson, D. S., & McLean, P. D. (2005). Treatment of obsessive-
compulsive disorder: Cognitive behavior therapy vs. exposure and response
prevention. Behaviour Research and Therapy, 43(12), 1559-1576.
Wilhelm, S., Buhlmann, U., Tolin, D. F., Meunier, S. A., Pearlson, G. D., Reese, H. E.,
Cannistraro, P., Jenike, M. A., Rauch, S. L. (2008). Augmentation of behavior
therapy with D-cycloserine for obsessive-compuslive disorder, American Journal of
Psychiatry, 165, 335-341.
Wolpe, J. (1969). The Practice of Behavior Therapy. New York, NY: Pergamon Press.
SLEEP REHEARSAL OF EXTINCTION LEARNING 25
Figure 1. Histogram of self-reported listening hours in the sleep rehearsal condition.
0
0.5
1
1.5
2
2.5
0-5 5-10 10-15 15-20 20-30 30-40 40-45 45-50 50-55
Fre
quen
cy
Number of Hours
SLEEP REHEARSAL OF EXTINCTION LEARNING 26
Figure 2. Number of listening hours based on self-reports and play counts for four
participants in the sleep rehearsal condition.
0
10
20
30
40
50
60
1 2 3 4
Num
ber
of H
ours
Participant
Self-reports
Play counts