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Multisensory Training in PD

N

National Yang Ming Chiao Tung University

Status

Unknown

Conditions

Parkinson Disease

Treatments

Other: Conventional training
Other: Multisensory training

Study type

Interventional

Funder types

Other

Identifiers

NCT05027555
21MMHIS153e

Details and patient eligibility

About

People with Parkinson's disease (PD) were characterized by many motor symptoms, including rigidity, postural instability, bradykinesia, and resting tremor. These motor symptoms might cause gait dysfunction. Gait dysfunction represented a common sign of PD, including reduced gait velocity, reduced stride length, reduced arm swing, and increased gait variability. Poor postural control in people with PD might result to increase gait variability and then increase fall risk. Previous studies reported that proprioceptive-vestibular multisensory training improved postural stability in people with PD. However, no literature investigated the effects of proprioceptive-vestibular multisensory training on gait variability. Therefore, the purpose of this study is to examine the effect of proprioceptive-vestibular multisensory training on gait variability in people with PD.

Enrollment

40 estimated patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Idiopathic PD
  • Hoehn and Yahr stage I to III
  • Age 60~80 y/o
  • Mini-Mental State Examination (MMSE) ≥24
  • Ability to ambulate independently (with or without walking aid)

Exclusion criteria

  • Affecting the peripheral vestibular system
  • Medical condition that substantially influenced their gait and balance performance
  • People had joined any rehabilitation past 1 month

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Multisensory training group
Experimental group
Description:
The intervention is a 50-minute session and 2-sessions/week, totaling 6 weeks
Treatment:
Other: Multisensory training
Conventional training group.
Active Comparator group
Description:
The intervention is a 50-minute session and 2-sessions/week, totaling 6 weeks
Treatment:
Other: Conventional training

Trial contacts and locations

0

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Central trial contact

Yang Yea-Ru, PhD

Data sourced from clinicaltrials.gov

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