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Visuomotor Control in Parkinson Disease

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary completion moved earlier from Jul 31, 2028 to Jul 31, 2027 Completion moved earlier from Dec 31, 2028 to Dec 31, 2027 · Eligibility criteria expanded, about 10 words · Secondary endpoints: details revised at 5 of 9 entries · 1 more Show 4 more changesShow less
    • Completion moved earlier from Dec 31, 2028 to Dec 31, 2027
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 5 of 9 entries
    • Publications: details revised at 2 of 2 entries
  2. Minor Start date: Jul 1, 2025 to Jul 19, 2025 Secondary endpoints: details revised at 5 of 9 entries · Publications: details revised at 2 of 2 entriesv3 Show 2 more changesShow less
    • Secondary endpoints: details revised at 5 of 9 entries
    • Publications: details revised at 2 of 2 entries
  3. Notable Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Start date changed from estimate of Apr 14, 2025 to Jul 1, 2025 · Publications: details revised at 2 of 2 entriesv2 Show 3 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Apr 14, 2025 to Jul 1, 2025
    • Publications: details revised at 2 of 2 entries
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Visuomotor processing is the ability to integrate visual information into motor plans and movement correction, which is highly required in daily activities such as writing and walking. As visual impairments have been reported in people with Parkinson's disease (PD), it is likely that those impairments may affect visuomotor processing ability and subsequently impair motor performance. Furthermore, people with PD and freezing of gait (FOG) have exhibited poorer visual perception than those without FOG, yet the differences of visuomotor control have not been well investigated. Additionally, little did the studies apply neurophysiological assessment to investigate the associated neural mechanisms. This study aims to investigate behavioral and neurophysiological differences in visuomotor control among people with PD and FOG (freezers), without FOG (non-freezers), and age-matched healthy controls. Sixty-three participants, 21 freezers, 21 non-freezers, and 21 age-matched healthy controls, will be enrolled in this study. Behavioral assessments, including a manual control task and visual perception tests will be used to evaluate visuomotor and visual perceptual abilities. Neurophysiological correlates, including corticomotor excitability and corticocortical connectivity between V1-M1 and PPC-M1, will be examined using transcranial magnetic stimulation. It is hypothesized that freezers will demonstrate the greatest visuomotor impairments and disrupted corticocortical connectivity compared to non-freezers and controls. By integrating behavioral and neurophysiological outcomes, this study seeks to unravel the mechanisms linking visual and motor impairments to FOG, ultimately providing insights into targeted interventions to improve visuomotor processing and motor performance in PD.
Trial Details
NCT Number NCT06918938
Lead Sponsor National Taiwan University Hospital
Conditions Parkinson Disease
Enrollment 63 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov