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NCT06942533Recruiting

Effect of Visual Feedback From the SpiroGym Mobile Application

The Effect of Visual Feedback From the SpiroGym Mobile Application on Expiratory Muscle Strength Training Performance in Patients With Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 1 Dec 2025

Brief summary (registry, in English)

The previous pilot study showed that two weeks of intensive expiratory muscle strength training (EMST) with SpiroGym was sufficient to significantly improve voluntary peak cough flow (PCF). The improvement was quantitatively comparable to that reported in other intensive EMST studies of longer duration. To explain this rapid improvement, we considered the potential contribution of SpiroGym's visual feedback. We assumed that real-time visual feedback increased training effort compared with conventional EMST performed without immediate feedback. The aim of this study is to evaluate the effect of visual feedback provided by the SpiroGym mobile application on performance during expiratory muscle strength training in patients with Parkinson's disease.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
9 Apr 2025
Start date
1 May 2025
Primary completion date
1 May 2026
Lead sponsor
General University Hospital, Prague
NCT number
NCT06942533

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 1 May 2025 to the primary completion date, 1 May 2026
  • 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.

Prior treatment

  • History of head or neck cancer or previous surgical interventions in the neck region.

Other illness

  • Other neurological disorders
  • Significant cognitive impairment
  • Major psychiatric disorder
  • Illness during the study period

Who the study is looking for

  • Diagnosis of Parkinsons disease
  • Stable dopaminergic medication (stable dose for at least 1 month)

Age in the registry: 40 years to 80 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
Department of Neurology and Centre of Clinical Neuroscience First Faculty of Medicine, Charles University and General University Hospital in Prague
Coordinator of this site? Confirm its status
PragueCzechiaRecruiting
General University Hospital
Coordinator of this site? Confirm its status
PragueCzechiaRecruiting

Related publications

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