Actively Recruiting
The Effect of an Auditory Rhythmic Cue on the Frequency of Rolling in Patients with Dysphagia and Parkinson's Disease
Led by Hopital La Musse · Updated on 2024-11-19
18
Participants Needed
1
Research Sites
126 weeks
Total Duration
On this page
Sponsors
H
Hopital La Musse
Lead Sponsor
F
France Parkinson Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main objective of this clinical study is to measure the effect of rhythmic auditory cueing, introduced in rehabilitation with three weekly sessions over a period of 7 weeks, on the frequency of rolling in idiopathic Parkinson's disease patients using pharyngography (swallowing radiography). The primary question of this study is: Does the rhythmic cueing introduced in rehabilitation significantly reduce the frequency of rolling in dysphagic Parkinson's patients? The researchers will assess the various stages of swallowing before, after, and 3 months after the rehabilitation protocol, focusing on the oral phase to determine if rhythmic auditory cueing reduces the frequency of rolling. Participants will be required to: * Perform three complete assessments (clinical speech therapy examination + pharyngography) before the protocol, after the protocol, and 3 months post-protocol. * Attend three times per week for 7 weeks at the La Musse hospital to participate in the protocol sessions under the supervision of a speech therapist.
CONDITIONS
Official Title
The Effect of an Auditory Rhythmic Cue on the Frequency of Rolling in Patients with Dysphagia and Parkinson's Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of idiopathic Parkinson's disease confirmed by neurologist using DAT SCAN and clinical exam
- Presence of a swallowing disorder with rolling
- Affiliated with the social security system
- Age 18 years or older
You will not qualify if you...
- Severe pharyngeal dysphagia causing aspiration with nectar and pudding textures
- Severe cognitive impairment with Mini Mental Parkinson test score below 24
- Known deafness or profound hearing loss
- Under legal protection measures
- History of reconstructive ENT surgery at the oropharyngeal level
- Neurological history causing swallowing disorder (e.g., stroke)
- Having a gastrostomy with no oral feeding
- Currently receiving speech therapy for swallowing
- Enrolled in another research protocol
- Pregnant or suspected pregnancy
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hôpital La Musse - La Renaissance Sanitaire
Saint-Sébastien-de-Morsent, Normandy, France, 27180
Actively Recruiting
Research Team
H
Héloïse BAILLET, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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