# Medical device-based neuromodulation for motor symptoms in Parkinson’s disease: a systematic review and meta-analysis

**Authors:** Paulo E. P. Teixeira, João Victor Ribeiro, João Pedro Serrao Perin, Walter Augusto Fabris Moraes, Elly Angelica Pichardo, Ciro Ramos-Estebanez, Felipe Fregni, Tim Wagner, Laura Dipietro

PMC · DOI: 10.3389/fneur.2026.1731885 · Frontiers in Neurology · 2026-02-12

## TL;DR

This study reviews and analyzes clinical trials to assess how well medical device-based treatments improve motor symptoms in Parkinson's disease.

## Contribution

The first review to calculate separate effect sizes for each active intervention group in multi-arm trials in this field.

## Key findings

- MDBN showed a small but significant improvement in motor symptoms (SMD = -0.18, p = 0.008).
- Effect sizes were larger with intention-to-treat analysis and smaller with sham stimulation comparators.
- Non-invasive and invasive MDBN approaches were both studied, with 30 and 17 trials respectively.

## Abstract

To synthesize randomized clinical trial (RCT) evidence comparing the efficacy of medical device-based neuromodulation (MDBN) techniques for improving motor symptoms in Parkinson’s disease (PD).

Device-based neuromodulation therapies, including deep brain stimulation (DBS), transcranial magnetic stimulation (TMS), and transcranial direct current stimulation (tDCS), are used to target PD motor symptoms, but reported effect sizes vary substantially across trials.

A systematic review was conducted in accordance with PRISMA guidelines. RCTs evaluating MDBN for PD motor function, measured by the Unified Parkinson’s Disease Rating Scale Part III (UPDRS3), were identified through MEDLINE, Embase, and Web of Science. A random-effects meta-analysis was performed for the primary outcome (UPDRS3). Risk of bias was assessed using the Cochrane RoB tool, and certainty of evidence with GRADE. Meta-regression examined methodological, population, and intervention variables associated with effect size variation.

Forty-seven RCTs (56 intervention comparisons; 2,638 participants) were included. Thirty trials investigated non-invasive neuromodulation (mainly rTMS and tDCS) and 17 invasive approaches (DBS). Meta-analysis of 39 effect sizes (from studies during L-Dopa ON, near-term follow-up) showed a small but significant improvement with active MDBN (SMD = −0.18, p = 0.008; I2 = 61%). Meta-regression showed larger effects in studies using intention-to-treat analysis and smaller effects when sham stimulation was used as a comparator.

MDBN is associated with modest yet significant motor improvements in PD. Effect size estimates are influenced by methodological characteristics, particularly analysis strategy and comparator selection. This is the first review in the field to calculate and incorporate separate effect sizes for each active intervention group in multi-arm trials, enabling more precise data inclusion.

## Linked entities

- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}, MAOB (monoamine oxidase B) [NCBI Gene 4129]
- **Diseases:** neurodegenerative condition (MESH:D019636), sleep disturbance (MESH:D012893), PD (MESH:D010300), Alzheimer's disease (MESH:D000544), postural instability (MESH:D054972), bradykinesia (MESH:D018476), resting tremor (MESH:D014202), aphasia (MESH:D001037), depression (MESH:D003866), dyskinesias (MESH:D004409), rigidity (MESH:D009127), cognitive decline (MESH:D003072)
- **Chemicals:** MDBN (-), L-Dopa (MESH:D007980), Dopamine (MESH:D004298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937557/full.md

## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937557/full.md

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Source: https://tomesphere.com/paper/PMC12937557