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Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia

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...

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Autores principales: Elsey, James W. B., Kindt, Merel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632940/
https://www.ncbi.nlm.nih.gov/pubmed/34867558
http://dx.doi.org/10.3389/fpsyt.2021.775770
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author Elsey, James W. B.
Kindt, Merel
author_facet Elsey, James W. B.
Kindt, Merel
author_sort Elsey, James W. B.
collection PubMed
description 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.
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spelling pubmed-86329402021-12-02 Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia Elsey, James W. B. Kindt, Merel Front Psychiatry Psychiatry 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. Frontiers Media S.A. 2021-11-12 /pmc/articles/PMC8632940/ /pubmed/34867558 http://dx.doi.org/10.3389/fpsyt.2021.775770 Text en Copyright © 2021 Elsey and Kindt. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Elsey, James W. B.
Kindt, Merel
Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title_full Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title_fullStr Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title_full_unstemmed Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title_short Placebo and Non-specific Effects in Reconsolidation-Based Treatment for Arachnophobia
title_sort placebo and non-specific effects in reconsolidation-based treatment for arachnophobia
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632940/
https://www.ncbi.nlm.nih.gov/pubmed/34867558
http://dx.doi.org/10.3389/fpsyt.2021.775770
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