Wearable Biofeedback for Swallowing Disorders Rehabilitation in Stroke and Parkinson Disease

Recruiting Phase 2 Interventional Study
Dysphagia Stroke Parkinson Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
50 – 90
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
University of Illinois at Urbana-Champaign · Other
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About This Trial
Dysphagia, or difficulty swallowing, is a common symptom of many neurological diseases but its treatment is not well established or easily accessible. To start addressing this gap, the researchers developed and validated a cost-effective wearable surface electromyography (sEMG) biofeedback sensor technology (i-Phagia), optimized to record muscle activity from the head/neck and provide biofeedback…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 50-90 years old * a confirmed (by a neurologist/physician) diagnosis of stroke at least 3 months post event, or of PD (Hoehn and Yahr Stages II-IV) * score in the normal/mild range on the Montreal Cognitive Assessment (MoCA), determined during an in-house screening * confirmed…
Contacts

Georgia Malandraki, PhD

217-265-7561

georgiam@illinois.edu

CONTACT

Jaime Bauer Malandraki, MS

217-265-7561

jaimebm@illinois.edu

CONTACT