# Visual perturbation training to reduce visual dependency in Parkinson’s disease: A randomized controlled trial

**Authors:** Remco J. Baggen, Anke Van Bladel, Maarten R. Prins, Jennifer Stappers, Joke Spildooren, Miet De Letter, Katie Bouche, Dirk Cambier, Leen Maes, Patrick Santens, Leonardo Peyré-Tartaruga, Anne Martin, Anne Martin

PMC · DOI: 10.1371/journal.pone.0343223 · PLOS One · 2026-03-02

## TL;DR

A study shows that visual perturbation training during treadmill walking reduces visual dependency and improves gait in people with Parkinson’s disease.

## Contribution

This is the first randomized controlled trial to demonstrate that visual perturbation training decreases visual dependency in Parkinson’s disease.

## Key findings

- Visual perturbation training significantly decreased visual dependency compared to treadmill-only training.
- Temporal gait parameters like step time, stride time, and cadence improved with visual perturbation training.
- Improvements in visual dependency were more pronounced in participants with earlier disease stages.

## Abstract

Decreased gait automaticity and increased visual dependency are important contributors to falls in people with Parkinson’s disease. The aim of this study was to assess if visual perturbation training during treadmill walking decreases visual dependency in people with Parkinson’s disease.

For this randomized controlled trial 25 early-to-mid-stage people with Parkinson’s disease (age 50-67y) without regular freezing of gait were randomly assigned to a visual perturbation group or treadmill training-only control group. Both groups trained 2 times per week for 6 weeks. Visual perturbation training consisted of self-paced treadmill walking with perturbations applied as rotations around the sagittal axis and medio-lateral translations of the virtual reality environment. The primary outcome was visual dependency. Secondary outcomes included steady-state spatiotemporal gait parameters (gait speed, step time/length/width/frequency, and cadence), as well as self-reported (near) falls.

Group x time interaction effects revealed that visual perturbation training significantly decreased visual dependency (p < 0.001) and improved temporal gait characteristics such as step time (p = 0.012), stride time (p = 0.021) and cadence (p = 0.018) compared to treadmill-only controls. However, no significant effects were found for step width, step length, gait speed, and (near) falls. Improvements in visual dependency were negatively correlated to disease progression (p = 0.004). Discussion: Visual perturbation training decreases visual dependency and improves temporal gait parameters in people with Parkinson’s disease. Participants in earlier disease stages appear to benefit most from visual perturbation training but additional research is needed.

This study was pre-registered at ClinicalTrials.gov (NCT05690308) on 09/01/2023.

## Linked entities

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

## Full-text entities

- **Genes:** SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}
- **Diseases:** VI (MESH:D028243), fear (MESH:C000719212), PD (MESH:D010300), Visual Dependency (MESH:D014786), injuries (MESH:D014947), dopaminergic deficits (MESH:D009461), hyper- or hypotension (MESH:D007022), stroke (MESH:D020521), disorientation (MESH:D003221), fatigue (MESH:D005221), impaired vestibular function (MESH:D015837), Fall-related injuries (MESH:C537863), gait abnormalities (MESH:D020233), dizziness (MESH:D004244), tremor (MESH:D014202), cognitive disability (MESH:D003072), Parkinson and Movement Disorder (MESH:D009069), Parkinson (MESH:D010302), impaired balance control (MESH:D007174), FoG (MESH:D020234), degeneration of dopamine-producing neurons (MESH:D009410), neurological or musculoskeletal disorders (MESH:D009140)
- **Chemicals:** Levodopa (MESH:D007980), PONE-D-25-41463R1 (-), dopaminergic (MESH:D004298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12952592/full.md

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Source: https://tomesphere.com/paper/PMC12952592