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Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials
What happens when an emerging programme of medical research overlaps with a surging social movement? In this article we draw on the anthropological term ‘chemosociality’ to describe forms of sociality born of shared chemical exposure. Psychedelic administration in the context of recent clinical tria...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520581/ https://www.ncbi.nlm.nih.gov/pubmed/37466178 http://dx.doi.org/10.1017/S0033291723001289 |
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author | Noorani, Tehseen Bedi, Gillinder Muthukumaraswamy, Suresh |
author_facet | Noorani, Tehseen Bedi, Gillinder Muthukumaraswamy, Suresh |
author_sort | Noorani, Tehseen |
collection | PubMed |
description | What happens when an emerging programme of medical research overlaps with a surging social movement? In this article we draw on the anthropological term ‘chemosociality’ to describe forms of sociality born of shared chemical exposure. Psychedelic administration in the context of recent clinical trials appears to have been particularly chemosocial in nature. We argue that one consequence is that psychedelic-assisted therapy (PAT) clinical research trials tend to breach key assumptions underlying the logic of causal inference used to establish efficacy. We propose the concept of dark loops to describe forms of sociality variously emerging from, and impacting participant experiences in, PAT trials. These dark loops are not recorded, let alone incorporated into the causal pathways in the interpretation of psychedelic trial data to date. We end with three positions which researchers might adopt in response to these issues: chemosocial minimisation where research is designed to attenuate or eliminate the effects of dark loops in trials; chemosocial description where dark loops (and their impacts) are openly and candidly documented and chemosocial valorisation where dark loops are hypothesised to contribute to trial outcomes and actively drawn upon for positive effect. Our goal is to fold in an appreciation of how the increasingly-discussed hype surrounding psychedelic research and therapeutics continues to shape the phenomena under study in complex ways, even as trials become larger and more rigorous in their design. |
format | Online Article Text |
id | pubmed-10520581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105205812023-09-27 Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials Noorani, Tehseen Bedi, Gillinder Muthukumaraswamy, Suresh Psychol Med Review Article What happens when an emerging programme of medical research overlaps with a surging social movement? In this article we draw on the anthropological term ‘chemosociality’ to describe forms of sociality born of shared chemical exposure. Psychedelic administration in the context of recent clinical trials appears to have been particularly chemosocial in nature. We argue that one consequence is that psychedelic-assisted therapy (PAT) clinical research trials tend to breach key assumptions underlying the logic of causal inference used to establish efficacy. We propose the concept of dark loops to describe forms of sociality variously emerging from, and impacting participant experiences in, PAT trials. These dark loops are not recorded, let alone incorporated into the causal pathways in the interpretation of psychedelic trial data to date. We end with three positions which researchers might adopt in response to these issues: chemosocial minimisation where research is designed to attenuate or eliminate the effects of dark loops in trials; chemosocial description where dark loops (and their impacts) are openly and candidly documented and chemosocial valorisation where dark loops are hypothesised to contribute to trial outcomes and actively drawn upon for positive effect. Our goal is to fold in an appreciation of how the increasingly-discussed hype surrounding psychedelic research and therapeutics continues to shape the phenomena under study in complex ways, even as trials become larger and more rigorous in their design. Cambridge University Press 2023-10 2023-07-19 /pmc/articles/PMC10520581/ /pubmed/37466178 http://dx.doi.org/10.1017/S0033291723001289 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use and/or adaptation of the article. |
spellingShingle | Review Article Noorani, Tehseen Bedi, Gillinder Muthukumaraswamy, Suresh Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title | Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title_full | Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title_fullStr | Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title_full_unstemmed | Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title_short | Dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
title_sort | dark loops: contagion effects, consistency and chemosocial matrices in psychedelic-assisted therapy trials |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520581/ https://www.ncbi.nlm.nih.gov/pubmed/37466178 http://dx.doi.org/10.1017/S0033291723001289 |
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