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NCT05700825RecruitingPhase 2

Rehabilitation of Airway Protection in Parkinson's Disease

Rehabilitation of Airway Protection in Parkinson's Disease: Comparing In-person and Telehealth Service Delivery Models

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

Airway protective disorders are a prevalent and progressive consequence of Parkinson's Disease (PD), and often result in aspiration pneumonia which is the leading cause of death in PD. Despite this, a large number of patients with PD do not access specialized services to address these critical deficits. The investigators will examine the comparative effectiveness of a novel treatment paradigm delivered in-person versus via telehealth in persons with PD, as well as the role of patient burden and treatment adherence on outcomes; thus, the proposed research is relevant to public health and in line with NIH's mission to identify novel, efficacious, and accessible rehabilitation strategies for short- and long-term improvement of dysfunctional airway protection in PD.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
120 (estimated)
First submitted
22 Dec 2022
Start date
11 Aug 2022
Primary completion date
1 Sept 2027
Lead sponsor
Teachers College, Columbia University
NCT number
NCT05700825

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 120
  • From 11 Aug 2022 to the primary completion date, 1 Sept 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Other neurological disorders (e.g., multiple sclerosis, stroke, brain tumor, etc.)
  • history of head and neck cancer
  • history of breathing disorders or diseases (e.g., COPD)
  • history of smoking in the last five years
  • uncontrolled hypertension
  • difficulty complying due to neuropsychological dysfunction (i.e., severe depression with \>28 on the Beck Depression Index (BDI-II), dementia with \<19 on the Montreal Cognitive Assessment (MoCA))
  • allergy to capsaicin or barium

Other

  • further than 1.5 hours (door to door) distance from either Teachers College, Columbia University or Purdue University.

Who the study is looking for

  • Diagnosed with PD (Hoehn and Yahr Stages II-IV)126,127 confirmed by a Movement Disorders fellowship trained neurologist having reviewed the video recorded Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) assessment for each participant and using strict UK brain bank criteria
  • airway protective deficits as defined as a minimum of penetration of thin liquids (penetration-aspiration score\>3) as determined by instrumental swallowing assessment and/or dystussia as determined by voluntary cough assessment (PEFR ≤4.1 L/s)
  • not actively receiving exercise-based swallowing therapy
  • between the ages of 50 and 90.

Age in the registry: 50 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Teachers College, Columbia University
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Purdue University
Coordinator of this site? Confirm its status
West LafayetteUnited StatesActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.