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Vibrotactile Foot Device for Freezing of Gait in Parkinson's Disease

Vibrotactile Foot Device for Freezing of Gait in Parkinson's Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06147713
Enrollment
200
Registered
2023-11-28
Start date
2022-05-01
Completion date
2024-11-01
Last updated
2024-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Freezing of Gait, Parkinson Disease

Brief summary

Freezing of gait (FOG) is a common, disabling symptom of later stage Parkinson's disease (PD), and can induce significant morbidity and mortality by increasing risk of falls as the disease progresses. Despite optimum medical management and deep brain stimulation therapy, many patients with PD are incapacitated by FOG and gait disorders. Non-invasive vibrotactile stimulation has been reported to potentially improve FOG of patients with PD. However, results of studies were variable, and there is a lack of convenient vibrotactile devices ready for daily use with reliable clinical trial data. In the proposed study, the investigator will test the effect of a newly developed vibrotactile foot device (Smart shoe) on participants diagnosed with PD and FOG. EEG and fMRI are obtained in order to investigate the underlying neurological mechanism.

Interventions

DEVICEVibrotactile foot device (Smart shoe)

A foot device deliver vibrotactile stimulation triggered by a foot pressure sensor.

Sponsors

Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 30-80 years * Diagnosed with Parkinson's Disease according to MDS Clinical Diagnostic Criteria * Stable drug therapy without any change in the past one month * Subjective presence of FOG more than once per day * Objective presence of FOG by provoking tasks, e.g., gait initiation, rapid full turn, et al. * Able to walk unaided at least 20 meters * Provide written informed consent

Exclusion criteria

* Stroke and other diseases interfering ambulation * Severe foot sensory impairments disabling the individual to perceive vibratory stimulation * History of deep brain stimulation surgery

Design outcomes

Primary

MeasureTime frameDescription
New Freezing of Gait Questionnaire (NFOGQ)2 weeksChanges in the New Freezing of Gait Questionnaire (NFOGQ) score
Freezing severity2 weeksChanges in the quantified freezing severity during walking task, videotape reviewed by movement disorder specialists

Secondary

MeasureTime frameDescription
Berg Balance Scale2 weeksChanges in the Berg Balance Scale score
Number of falls and near falls2 weeksChanges in number of falls and near falls during intervention period
Quantitative Gait parameters2 weeksChanges in gait parameters such as stride length, et al. during walking tasks
Clinical Global Impressions Scale (CGI-I)2 weeksChanges in the Clinical Global Impressions Scale (CGI-I) score
39-item Parkinson's Disease Questionnaire (PDQ-39)2 weeksChanges in the 39-item Parkinson's Disease Questionnaire (PDQ-39) score
MDS-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) part III2 weeksChanges in the MDS-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) part III score

Countries

China

Contacts

Primary ContactPiu Chan, MD. PhD.
pbchan@hotmail.com+86-010-83198677
Backup ContactShanshan Cen, MD. PhD.
censs843@hotmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026