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Clinical Trials/NCT06918938
NCT06918938RecruitingNot Applicable

Unraveling Visuomotor Control in Parkinson Disease With and Without Freezing of Gait

National Taiwan University Hospital2 sites in 1 country63 target enrollmentStarted: July 19, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
63
Locations
2
Primary Endpoint
Root-mean square-error

Study Overview

Brief Summary

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • age above 18
  • able to follow the researchers' instructions
  • normal or correct-to-normal vision to view a computer screen

Exclusion Criteria

  • neurological disorders other than PD
  • diagnosed psychological disorders or a tendency of anxiety and/or depression
  • a self-history of seizure or a family history of epilepsy
  • deep brain stimulation or pacemaker implanted
  • unstable cardiovascular diseases or other uncontrolled medical conditions
  • surgical history, severe injury, or severe tremor of their upper extremities that can affect their movements in the past 6 months

Arms & Interventions

FOG

Participants with Parkinson disease and freezing of gait

NFOG

Participants with Parkinson disease without freezing of gait

CON

Age-matched healthy adults

Outcomes

Primary Outcomes

Root-mean square-error

Time Frame: Day 1

Overall performance accuracy relative to the target waveform, which is the mean difference between the target waveform and the participant's movement trajectory calculated over their actual movement time.

Squared mean jerk

Time Frame: Day 1

The squared mean of the jerk of the visuomotor trajectory, which a minor JSM is assumed a major smoothness by better controlling the movement.

Directional error

Time Frame: Day 1

The value of the instantaneous component of the hand movement vector, perpendicular to the target trajectory in every sampled time point, which will be calculated and expressed as a percentage of the total movement vector

Movement time

Time Frame: Day 1

Total movement time of a trial will be recorded.

Tracking interruption

Time Frame: Day 1

Frequency and duration of tracking interruptions will be recorded when the participant's cursor exits the target circle.

Secondary Outcomes

  • Benton Judgment of Line Orientation Test(Day 2)
  • National Eye Institute Visual Function Questionnaire-25(Day 2)
  • Random dot cinematogram(Day 2)
  • Purdue Pegboard Test(Day 2)
  • Timed Up and Go Test(Day 2)
  • Movement Disorder Society Unified Parkinson's Disease Rating Scale(Day 1)
  • New Freezing of Gait Questionnaire(Day 1)
  • Cortical excitability(Day 1 and Day 2)
  • Corticocortical connectivity(Day 1 and Day 2)
  • Movement Disorder Society Unified Parkinson's Disease Rating Scale(Day 1)
  • New Freezing of Gait Questionnaire(Day 1)
  • Cortical excitability(Day 1 and Day 2)
  • Corticocortical connectivity(Day 1 and Day 2)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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