Trial reportTranslational psychiatry2026
The role of the dorsal attention network in attention bias modification for social anxiety disorder.
Trial report in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Identifying reliable biomarkers of treatment response is central to advancing personalized psychiatry. While whole-brain functional connectivity models have shown promise in predicting clinical outcomes, especially for broad-spectrum interventions like cognitive-behavioral therapy, targeted treatments may benefit from more specific neuromarkers. In social anxiety disorder (SAD), Gaze-Contingent Music Reward Therapy (GC-MRT) is a novel attention bias modification (ABM) intervention designed to reduce preferential attentional allocation to socially threatening stimuli. Given the dorsal attention network's (DAN) key role in top-down attentional control, we tested whether resting-state intra-network DAN connectivity could serve as a neural predictor of response to GC-MRT. Participants with SAD were randomized to either receive GC-MRT (n = 22) or to a waitlist control condition (n = 24). Resting-state fMRI data were collected before and after the intervention. Intra-DAN connectivity at baseline and post-treatment were associated with post-treatment symptom severity in the GC-MRT group. Post-treatment intra-DAN connectivity significantly differed in the GC-MRT group relative to controls. These findings suggest that intra-network connectivity within the DAN may have the potential to function both as a predictive biomarker and as a neural marker of successful intervention. Our findings highlight the role of the DAN in attention-based clinical interventions and show that network-specific connectivity metrics may offer a more precise understanding of how targeted neuromodulation affects symptom change in SAD.
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