ePoster

NEURAL CORRELATES OF THE IMPROVEMENT OF MOTOR AND NON-MOTOR SYMPTOMS IN PARKINSON’S DISEASE FOLLOWING A COMBINED DIGITAL AND LEVODOPA THERAPY

Tal Tamirand 8 co-authors

Remepy health Ltd.

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS01-07AM-466

Presentation

Date TBA

Board: PS01-07AM-466

Poster preview

NEURAL CORRELATES OF THE IMPROVEMENT OF MOTOR AND NON-MOTOR SYMPTOMS IN PARKINSON’S DISEASE FOLLOWING A COMBINED DIGITAL AND LEVODOPA THERAPY poster preview

Event Information

Poster Board

PS01-07AM-466

Abstract

Despite the availability of pharmacological treatments, Parkinson’s disease (PD) remains associated with significant unmet clinical needs. We aimed to demonstrate the parallel neural mechanisms underlying the effects of combining standard levodopa treatment with the DopApp digital intervention on motor and non-motor symptoms.
Forty-two PD patients treated with levodopa participated in a prospective, double-blind, randomized, placebo-controlled trial. The 3-week digital treatment consisted of a proprietary daily protocol combining multisensory motor, psychological, and cognitive training. This included fine-motor exercises and rehabilitation-focused modules, along with sensory-depravation tasks and daily walking. Patients were assessed pre- and post-treatment using clinical and psychological scales and resting-state fMRI (rsFC) scans.
DopApp treatment significantly improved the total MDS-UPDRS score compared to placebo-app (inter-group difference of 7.8 points, p=0.0005). Several exploratory endpoints were also statistically significant, including MDS-UPDRS-II,III and Beck Depression Inventory (BDI-II) scores. These effects were associated with parallel modulation of rsFC within the thalamocortical motor and limbic networks. Moreover, increased engagement with sensorimotor and emotion regulation activities correlated with both enhanced clinical effects and rsFC alterations, suggesting a digital dose-response relationship and task-specific neural plasticity.
This study provides preliminary clinical and neurobiological evidence that a targeted, digital therapeutic can augment standard dopaminergic treatment in PD. Dose-response relationships between engagement and outcomes suggest that adaptive, task-specific digital tools may drive circuit-selective plasticity. These findings support the integration of scalable digital interventions into precision drug-digital strategies for neurodegenerative disease treatment, representing an early step toward hybrid approaches that personalize care, enhance efficacy, and extend reach beyond traditional setting.

Multi-panel figure (a–f) summarizing clinical and connectivity outcomes for DopApp™ versus placebo. (a) Scatter and bar plot showing a greater mean reduction (improvement) in total MDS-UPDRS score from baseline in the DopApp™ group compared with placebo. (b) Cumulative distribution of change in total MDS-UPDRS score demonstrating a higher proportion of DopApp™ participants achieving clinically meaningful improvement thresholds relative to placebo. (c) Positive correlation between increased thalamic VL–M1 resting-state functional connectivity and engagement with the DopApp™ sensorimotor deprivation task. (d) Positive correlation between increased thalamic AV–mPFC connectivity and engagement with DopApp™ emotion regulation activities. (e) Negative correlation between increased thalamic VL–M1 connectivity and reduction in MDS-UPDRS III scores, indicating greater improvement in motor symptoms in the DopApp™ group, with no significant relationship in the placebo group. (f) Negative correlation between increased thalamic AV connectivity and reduction in BDI-II scores, indicating greater improvement in depressive symptoms in the DopApp™ group, with no significant relationship in the placebo group.

Recommended posters

Cookies

We use essential cookies to run the site. Analytics cookies are optional and help us improve World Wide. Learn more.