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Studies swallowing and voice-box function in people with neurodegenerative diseases

Records swallowing tests and questionnaires in adults with Parkinson disease and similar conditions.

Plain-language title generated from the registry record
Registry title: Systematic Assessment of Laryngopharyngeal Function in Patients With Neurodegenerative Diseases

Key facts

Where
Innsbruck, AustriaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with a neurodegenerative disease, such as multiple system atrophy, progressive supranuclear palsy, Parkinson's disease or motor neurone disease. They must have had a swallowing and throat check with a camera (FEES) using a set task protocol.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Probable or possible multiple system atrophy, probable or possible progressive supranuclear palsy, Parkinson's disease (Hoehn and Yahr stage I-V), motor neurone disease, or another neurodegenerative disease.

Main reasons for not taking part

  • People who do not sign the consent form cannot join.
  • Healthy volunteers cannot join.

Read by machine on 9 November 2026.

Where in Austria

  • Department of Neurology and Department of ENT, Medical University InnsbruckInnsbruck, AustriaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Kliniken Beelitz GmbH
Trial code
NCT04706234
Record updated
9 April 2025
Original description
This is a non-interventional observational study designed to systematically record the results of routine laryngeal examinations and specific characteristics of dysphagia in patients with neurodegenerative disorders. The results of a fiberoptic / flexible endoscopic evaluation of swallowing (FEES) while performing a structured task protocol will be recorded. If available, laryngeal electromyography (EMG) results will also be recorded. In addition to the examination results, demographic and disease-specific data are collected, and two questionnaires, the Swallowing Disturbance Questionnaire for Parkinson's Disease (SDQ-PD) and the swallowing specific Quality Of Life Questionnaire (SWALQOL), are administered.Read full original descriptionShow less

Prospective Observational Study for the Systematic Assessment of Laryngopharyngeal Function in Patients With Neurodegenerative Diseases

This is a non-interventional observational study designed to systematically record the results of routine laryngeal examinations and specific characteristics of dysphagia in patients with neurodegenerative disorders. The results of a fiberoptic / flexible endoscopic evaluation of swallowing (FEES) while performing a structured task protocol will be recorded. If available, laryngeal electromyography (EMG) results will also be recorded. In addition to the examination results, demographic and disease-specific data are collected, and two questionnaires, the Swallowing Disturbance Questionnaire for Parkinson's Disease (SDQ-PD) and the swallowing specific Quality Of Life Questionnaire (SWALQOL), are administered.

Inclusion: diagnosis of probable or possible multiple system atrophy according to current consensus criteria (Gilman et al. 2008) or; diagnosis of probable or possible PSP according to the the Movement Disorders Society (MDS) diagnostic criteria (Höglinger et al. 2017) or; diagnosis of Parkinson's disease according to the MDS diagnostic criteria (Postuma et al 2015); Hoehn and Yahr Stage within the range of I-V or; diagnosis of motor neurone disease or; diagnosis of a neurodegenerative disease other than specified above; AND underwent laryngopharyngeal assessment according to the systematic task protocol during FEES (Warnecke et al. 2019).

Exclusion: Patients who do not sign the consent form.

ClinicalTrials.gov NCT04706234