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Recruiting NCT06481540

NCT06481540 SpiroGym App-Aided Cough Rehabilitation

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Clinical Trial Summary
NCT ID NCT06481540
Status Recruiting
Phase —
Sponsor General University Hospital, Prague
Condition Parkinson Disease
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-01-01
Primary Completion 2025-05

Eligibility & Interventions

Sex All sexes
Min Age 40 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Expiratory muscle strength training + SpiroGym applicationExpiratory muscle strength training

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2024-01-01 with a primary completion date of 2025-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The pilot study by Srp et al. (2021) proved that the SpiroGym app was feasible for supporting expiratory muscle strength training (EMST) in Parkinson's disease (PD) patients. Two weeks of intensive EMST coupled with SpiroGym were sufficient to significantly improve the participants' voluntary peak cough flow (PCF). The improvement was quantitatively comparable to the results of other intensive EMST studies with longer durations. When interpreting such rapid improvement, the impact of SpiroGym's visual feedback was considered. It was assumed that visual feedback increased training effort compared to regular training without immediate control. However, comparative studies were required to verify the possible additional effects of visual feedback on voluntary PCF compared to EMST without feedback.

Eligibility Criteria

Inclusion Criteria: * Diagnosis of Parkinsons disease * Stable dopaminergic medication (stable dose for at least 1 month) Exclusion Criteria: * Other neurological disorders * Difficulty complying due to neuropsychological dysfunction (dementia with a score of less - - than 19 on the Montreal Cognitive Assessment) * Breathing disorders or diseases * Smoking in the past 5 years * Uncontrolled hypertension

Contact & Investigator

Central Contact

Martin Srp, PhD

✉ martin.srp@vfn.cz

📞 +420224965513

Frequently Asked Questions

Who can join the NCT06481540 clinical trial?

This trial is open to participants of all sexes, aged 40 Years or older, up to 80 Years, studying Parkinson Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06481540 currently recruiting?

Yes, NCT06481540 is actively recruiting participants. Contact the research team at martin.srp@vfn.cz for enrollment information.

Where is the NCT06481540 trial being conducted?

This trial is being conducted at Prague, Czechia.

Who is sponsoring the NCT06481540 clinical trial?

NCT06481540 is sponsored by General University Hospital, Prague. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology