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Electrical Stimulation for the Relief of Freezing of Gait (FOG) in Parkinson's Patients

Electrical Stimulation for the Relief of Freezing of Gait (FOG)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01970891
Enrollment
12
Registered
2013-10-28
Start date
2013-10-01
Completion date
2020-11-30
Last updated
2020-09-18

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

Conditions

Parkinson's Disease

Keywords

Freezing of Gait, Gait, Comfort, Pain tolerance, Pain, Sensory threshold, Motor threshold, Pain threshold

Brief summary

Potential for electrical stimulation to ameliorate Freezing of Gait (FOG)

Detailed description

The purpose of this study is to investigate the potential for an electrical stimulation intervention to ameliorate Freezing of Gait (FOG) and related gait disturbances in Parkinson's patients.

Interventions

DEVICEneuromuscular stimulation device

Effect of neuromuscular stimulation device at specific muscle sites will be examined for freezing of gait amelioration.

Sponsors

University Hospital of Limerick
CollaboratorOTHER
National University of Ireland, Galway, Ireland
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Sensory electrical stimulation for the amelioration of FoG through the continuous delivery of stimulation.

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* A diagnosis of idiopathic Parkinson's Disease (PD) (UK, PD Brain Bank Criteria) * A Hoehn and Yahr stage of 2 - 4 * Exhibiting Freezing of Gait or another gait abnormality in the ON state. * An ability to mobilise independently with or without a walker or walking cane for the purpose of research when in the 'ON' state

Exclusion criteria

* A serious cognitive impairment (MMSE\<24) * Pregnant or currently involved in another clinical trial. * Pacemakers * On opioid or neuropathic pain medication

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Time in FoG PTFAt time of intervention (seconds)We hypothesise that the delivery of continuous sensory electrical stimulation will reduce the percentage of time in FoG.
Number of FoG episodes occurringAt time of intervention (seconds)We hypothesise that the delivery of continuous sensory electrical stimulation will reduce the Number of FoG episodes Occurring (NFO).

Countries

Ireland

Outcome results

None listed

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