Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
All Genders
NCT06942533

Effect of Visual Feedback From the SpiroGym Mobile Application

Led by General University Hospital, Prague · Updated on 2025-12-01

30

Participants Needed

2

Research Sites

60 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Effect of Visual Feedback From the SpiroGym Mobile Application

Who Can Participate

Age: 40Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Parkinsons disease
  • Stable dopaminergic medication (stable dose for at least 1 month)
Not Eligible

You will not qualify if you...

  • Other neurological disorders
  • Significant cognitive impairment
  • Major psychiatric disorder
  • History of head or neck cancer or previous surgical interventions in the neck region
  • Illness during the study period

AI-Screening

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Trial Site Locations

Total: 2 locations

1

General University Hospital

Prague, Czechia, 120 00

Actively Recruiting

2

Department of Neurology and Centre of Clinical Neuroscience First Faculty of Medicine, Charles University and General University Hospital in Prague

Prague, Czechia, 16000

Actively Recruiting

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Research Team

M

Martin Srp, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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