Abstract

The idea that maladaptive memories may be rendered susceptible to interference after reactivation raises the possibility of reactivating and neutralizing clinically-relevant emotional memories. In this study, we sought to investigate the feasibility of such a “reconsolidation-based” intervention for arachnophobia, drawing upon previous research that successfully reduced fear of spiders in a subclinical sample. In Experiment 1, we piloted several reactivation procedures for conducting a reconsolidation-based treatment for arachnophobic individuals. All procedures involved some form of brief exposure to a fear-provoking spider, followed by the administration of 40 mg propranolol. In Experiment 2, we conducted a double-blind, placebo-controlled assessment of one procedure tested in Experiment 1. In Experiment 1, we found that most reactivation procedures produced drops in self-reported fear of spiders from pre- to post-treatment, including fear declines that were apparent up to 6- and even 14-months later. However, in Experiment 2, we found no evidence that the participants receiving propranolol were better off than those who received placebo. While our findings are limited by the small sample sizes used, they nevertheless show a different pattern of responses than was observed in a previous reconsolidation-based intervention for subclinical spider fearful participants. Alterations to the protocol made to accommodate the clinical participants may have led to greater opportunities for non-specific effects (e.g., exposure, placebo effects) to drive change in the participants. Our findings highlight both the challenges of translating reconsolidation-based procedures into clinical interventions, as well as the importance of controls for non-specific effects in reconsolidation-based research.

Highlights

  • Cognitive behavioral therapies (CBT) are currently the most empirically supported method of treatment for anxiety disorders [1]

  • There was no evidence for differences in baseline Spider Phobia Questionnaire (SPQ), Patient Health Questionnaire (PHQ), or State-Trait Anxiety Index (STAI)-T scores, with slight evidence for differences in Anxiety Sensitivity Index (ASI) scores, which tended to be slightly lower in the Standard and Observe groups than in the Enclosure and Loose Tarantula groups

  • Correlations were run to determine whether baseline SPQ, ASI, PHQ, STAI-T, or Age might be predictive of change over time in, or baseline assessments of, key variables in the analyses below (Supplementary Material section ANOVAs and Contingency Tables for Baseline Measures)

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Summary

Introduction

Cognitive behavioral therapies (CBT) are currently the most empirically supported method of treatment for anxiety disorders [1]. Many patients undergoing CBT fail to benefit, and of those who do show an initial response, many relapse [2,3,4]. Influential models of the principal components of CBT—cognitive therapy [5] and exposure [6, 7]—may help to explain relapse. These models suggest that, rather than directly altering maladaptive cognitions, learned behaviors, and affective responses, cognitive behavioral interventions generate alternative adaptive representations in memory that compete with maladaptive ones for control over behavior. Because maladaptive memory traces remain intact even after successful therapy, they can resurface with the passage of time, in novel situations, or when the patient is highly stressed, leading to relapse

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