Resumen
We aim to develop fMRI neurofeedback as a treatment for obsessive compulsive disorder (OCD). In prior work, we found that providing neurofeedback of activity in the anterior prefrontal cortex (aPFC) improved control over contamination anxiety in a subclinical population. Here, we present the results of a randomized, double-blind clinical trial (NCT02206945) testing this intervention in patients with OCD. We recruited patients with primary symptoms in the fear-of-harm/checking or contamination/washing domains. During neurofeedback, they viewed symptom provocative images and attempted to up- and down-regulate the aPFC during different blocks of time. The active group received two sessions of neurofeedback and the control group received yoked sham feedback. The primary outcome measure was the Yale-Brown Obsessive-Compulsive Symptom scale. The secondary outcome was control over aPFC. Thirty-six participants completed feedback training (18 active, 18 control). The active group had a slightly but significantly greater reduction of obsessive-compulsive symptoms after neurofeedback compared to the control group (p<.05) but no significant differences in control over the aPFC. These data demonstrate that neurofeedback targeting the aPFC can reduce symptoms in OCD. Future investigations should seek to optimize the training protocol to yield larger effects and to clarify the mechanism of action.
| Idioma original | English |
|---|---|
| Número de artículo | 115458 |
| Publicación | Psychiatry Research |
| Volumen | 328 |
| DOI | |
| Estado | Published - oct 2023 |
Nota bibliográfica
Publisher Copyright:© 2023 Elsevier B.V.
Financiación
This work was supported by NIMH ( R01 MH100068 , M. Hampson; K24 MH121571 , C. Pittenger), the state of Connecticut through its support of the Ribicoff Research Facilities at the Connecticut Mental Health Center, and by the Taylor Family Foundation (C. Pittenger). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health, the State of Connecticut, or other sponsors . This work was supported by NIMH (R01 MH100068, M. Hampson; K24 MH121571, C. Pittenger), the state of Connecticut through its support of the Ribicoff Research Facilities at the Connecticut Mental Health Center, and by the Taylor Family Foundation (C. Pittenger). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health, the State of Connecticut, or other sponsors.
| Financiadores | Número del financiador |
|---|---|
| Connecticut Mental Health Center | |
| Taylor Family Foundation | |
| National Institutes of Health (NIH) | |
| National Institute of Mental Health | R01 MH100068, K24 MH121571 |
| National Institute of Mental Health | |
| Southern Connecticut State University |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Psychiatry and Mental health
- Biological Psychiatry
Huella
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