Fear reactivation prior to exposure therapy: Does it facilitate the effects of VR exposure in a randomized clinical sample?
Introduction
Although there is little doubt about the efficacy of exposure-based treatments for specific phobias, return of fear after successful treatment is still a major problem (Choy et al., 2007, Lipsitz et al., 1999). Several strategies aiming to prevent, or at least, diminish the return of fear have been explored so far. These include exposure in multiple contexts (Shiban et al., 2013, Thomas et al., 2009), exposure with a reminder cue of the extinction context (Brooks & Bouton, 1993) or pharmacological interventions, e.g., the administration of Propranolol, a beta-blocker, prior to or directly after fear reactivation in order to disrupt memory reconsolidation (Kindt, Soeter, & Vervliet, 2009).
Reactivation of long-term memory initiates a process similar to memory consolidation, namely memory reconsolidation (Bentz, Michael, de Quervain, & Wilhelm, 2010), which requires de novo protein synthesis to restabilize memory traces. The synthesized proteins for these two processes differ at the gene expression level, e.g., BDNF being expressed in the case of consolidation, and Zif268 for reconsolidation (Barnes et al., 2012, Lee and Hynds, 2013).
Pharmacological intervention, such as the blockade of beta-adrenergic receptors, shortly before or just after memory reactivation has been used to alter the reconsolidation process. For example Debiec and LeDoux (2004) demonstrated that an intra-amygdalar infusion of the beta-blocker Propranolol interferes with memory reconsolidation in rats. Comparable results were also reported in human samples. Propranolol either administered prior to memory reactivation (Kindt et al., 2009, Soeter and Kindt, 2010, Soeter and Kindt, 2011) or after memory reactivation (Sevenster et al., 2013, Soeter and Kindt, 2012) reduced conditioned fear responding and prevented the return of fear.
Recent experiments have focused on interfering with the process of memory reconsolidation by a behavioral procedure rather than pharmacologically blocking it. This approach relies on the lability, i.e. the susceptibility to alteration, of the memory trace during reconsolidation. The time window for this state of lability is believed to last 6 h after memory reactivation (Nader, Schafe, & Le Doux, 2000). Monfils, Cowansage, Klann, and LeDoux (2009) examined the effect of reactivation in rats and found that only rats which received extinction training within the reconsolidation window (i.e., 10 min or 1 h after memory reactivation) showed significantly reduced freezing in response to the CS at test, while rats who received extinction training outside this window (6 h or 24 h) did not show reduced freezing. Furthermore, extinction effects remained stable even up to one month after the extinction training. These results implicate that extinction training during memory reconsolidation leads to an incorporation of the new valence of the CS into the original fear memory trace (Monfils et al., 2009). However, there are animal studies that do not support this finding (Chan et al., 2010, Morris et al., 2005).
Nevertheless Schiller et al. (2010) were able to adapt this procedure to a human sample. In their seminal study, three groups of participants underwent a fear conditioning protocol. In one group, fear was reactivated 10 min prior to the extinction training by exposing the participants to a single presentation of the CS+. In the second group, reactivation took place 6 h prior to the extinction training, and in the third group fear was not reactivated at all. In a spontaneous recovery test 24 h after the extinction training, they found that fear was only eliminated in the first group, as indicated by no return of fear (reflected in mean differential SCRs). This result was stable in a follow-up test one year later. Kindt and Soeter (2013) were unable to replicate the findings of Schiller et al. (2010). Instead, they showed that a single retrieval period prior to extinction did not attenuate spontaneous recovery of extinguished conditioned responses, namely startle potentiating, skin conductance response, and US expectancy ratings. Other studies (Golkar et al., 2012, Soeter and Kindt, 2011) were also not able to replicate Schiller's findings. However, using an auditory fear conditioning paradigm, Oyarzun et al. (2012) were able to replicate Schiller at al. (2010).
As far as we know, these results were not translated to clinical practice yet. Such a translational step could advance exposure therapy substantially if the reactivation of fear memory within the reconsolidation window prior to exposure therapy would erase the fear memory and in turn prevent relapses. Therefore, the aim of our study is to apply the Schiller et al. (2010) reconsolidation protocol to exposure therapy of a clinical sample of spider phobic patients. Based on their results we expect that fear reactivation before exposure reduces spontaneous recovery of fear and improves long-term treatment success.
Section snippets
Design
Participants meeting the entry criteria were randomly (simple randomization 1-1) assigned to two groups (reactivation vs. control). Participants and researcher conducting the analysis were blind to the condition (double blind design) up to the moment of pre-exposure as the researcher could see the presented stimulus on the PC monitor. Data was collected during four sessions within two weeks and a 6-month follow-up questionnaire. G*Power 3.1.7 was used to calculate the sample size.5
Process analysis of VRET
Fear ratings and SCL data were subjected to repeated-measures ANOVAs with the within-subject factors exposure trial (exposure trial 1 to exposure trial 10) and time (beginning of exposure trial vs. end of exposure trial) and the between-subjects factor group (RG vs. CG).
Fear ratings. Fig. 3a depicts the fear ratings assessed during the exposure trials, i.e. the average of two ratings, one assessed after the first 10 s and one 10 s before the end of a given exposure trial. These ratings
Discussion
Our results did not confirm the hypothesis that a single reactivation trial prior to exposure therapy for spider phobia attenuates return of fear assessed 24 h later. This finding is in line with several fear-conditioning studies (Golkar et al., 2012, Kindt and Soeter, 2013, Soeter and Kindt, 2011), which were not able to replicate the facilitating effect of a single presentation of the CS prior to extinction.
However, since our study investigated exposure therapy, not fear conditioning and
Acknowledgments
This study is part of Dr. J. Brütting’s PhD thesis.
The authors would like to thank Evelyn Glotzbach-Schoon, Mathias Müller, Henrik Peperkorn, and Christian Tröger for their valuable support in designing and programming the virtual exposure scenario, and Iris Schelhorn for recruiting participants and collecting data. In addition, we would like to thank the participants in this study, for their courage to face their fear and our spider “Murphy” which helped many participants overcoming their fear
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