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Effects of Unsupervised Inspiratory Muscle Training on Ventilation Variability in Post-covid-19 Patients. - Trial NCT06362499

Access comprehensive clinical trial information for NCT06362499 through Pure Global AI's free database. This phase not specified trial is sponsored by Universidade Federal do Rio Grande do Norte and is currently Recruiting. The study focuses on COVID-19. Target enrollment is 24 participants.

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Trial Details
ClinicalTrials.gov โ€ข NCT06362499
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Effects of Unsupervised Inspiratory Muscle Training on Ventilation Variability in Post-covid-19 Patients.
Effects of Unsupervised Inspiratory Muscle Training on Ventilation Variability in Post-covid-19 Patients: Protocol for Randomized Clinical Trial.

Study Focus

COVID-19

Experimental Group

Interventional

device

Sponsor & Location

Universidade Federal do Rio Grande do Norte

Natal,Natal, Brazil

Timeline & Enrollment

N/A

Apr 01, 2024

Jul 31, 2024

24 participants

Primary Outcome

Ventilation variability and ventilation efficiency

Summary

Dysfunctional breathing and persistent hypocapnia can be associated with many of the symptoms
 experienced by patients such as dyspnea, fatigue, chest pain and palpitations. The
 identification of dysfunctional breathing and hypocapnia in these patients is important as it
 may represent a target for treatment.
 
 In many of these patients, tachypnea at low levels of exertion suggests increased respiratory
 muscle activity, which can lead to the sensation of dyspnea. Sympathetic hyperactivity leads
 to excessive and irregular ventilation during exercise. In this way, inspiratory muscle
 training can improve symptoms (dysfunctional breathing), possibly by attenuating the
 metaboreflex (vagal modulation-attenuation of the sympathetic response) of the inspiratory
 muscle in post-covid-19 subjects, reducing ventilatory variability.

ICD-10 Classifications

COVID-19, virus identified
COVID-19, virus not identified
Coronavirus infection, unspecified site
Viral infection, unspecified
Rift Valley fever

Data Source

ClinicalTrials.gov

NCT06362499

Device Trial