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The placebo effect and its clinical associations in gambling disorder

The placebo effect and its clinical associations in gambling disorder
The placebo effect and its clinical associations in gambling disorder

Background: although gambling disorder is prevalent and functionally impairing, no FDA-approved medications exist for its treatment. The ability of clinical trials to detect the benefits of active treatment has been hindered by an unusually high placebo response. Virtually nothing is known about baseline clinical characteristics that might predict placebo response in those with gambling disorder.

Methods: participants (N = 152) assigned to placebo were pooled from multiple double-blind trials of gambling disorder. Participants were classified as placebo responders or non-responders based on a cut-off of 35% reduction in symptom severity on the Gambling Symptom Assessment Scale. Baseline group differences were characterized using t tests and equivalent non-parametric tests as appropriate.

Results: fifty-one percent of individuals assigned to placebo showed a significant clinical response. Compared with non-responders, placebo responders remained in treatment for significantly longer, were more likely to report "enjoyment" as a trigger for gambling, and were less likely to state that "boredom" or "loneliness" triggered their gambling. Placebo responders and non-responders did not differ significantly in age, sex, age at symptom onset, baseline symptom severity, comorbidities, or likelihood of having received a previous treatment.

Conclusions: Predictors of placebo response for gambling disorder appear markedly different from those reported for other mental illnesses.

1040-1237
167-172
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Grant, Jon E.
07372bd5-8a0d-42b4-b41b-e376c652acf3
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f

Grant, Jon E. and Chamberlain, Samuel R. (2017) The placebo effect and its clinical associations in gambling disorder. Annals of clinical psychiatry : official journal of the American Academy of Clinical Psychiatrists, 29 (3), 167-172.

Record type: Article

Abstract

Background: although gambling disorder is prevalent and functionally impairing, no FDA-approved medications exist for its treatment. The ability of clinical trials to detect the benefits of active treatment has been hindered by an unusually high placebo response. Virtually nothing is known about baseline clinical characteristics that might predict placebo response in those with gambling disorder.

Methods: participants (N = 152) assigned to placebo were pooled from multiple double-blind trials of gambling disorder. Participants were classified as placebo responders or non-responders based on a cut-off of 35% reduction in symptom severity on the Gambling Symptom Assessment Scale. Baseline group differences were characterized using t tests and equivalent non-parametric tests as appropriate.

Results: fifty-one percent of individuals assigned to placebo showed a significant clinical response. Compared with non-responders, placebo responders remained in treatment for significantly longer, were more likely to report "enjoyment" as a trigger for gambling, and were less likely to state that "boredom" or "loneliness" triggered their gambling. Placebo responders and non-responders did not differ significantly in age, sex, age at symptom onset, baseline symptom severity, comorbidities, or likelihood of having received a previous treatment.

Conclusions: Predictors of placebo response for gambling disorder appear markedly different from those reported for other mental illnesses.

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More information

Published date: 1 August 2017

Identifiers

Local EPrints ID: 493246
URI: http://eprints.soton.ac.uk/id/eprint/493246
ISSN: 1040-1237
PURE UUID: 5f5b3dc3-abb5-4e37-8923-8ef58e93c513
ORCID for Samuel R. Chamberlain: ORCID iD orcid.org/0000-0001-7014-8121

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Date deposited: 29 Aug 2024 16:30
Last modified: 30 Aug 2024 02:00

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Contributors

Author: Jon E. Grant
Author: Samuel R. Chamberlain ORCID iD

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