Effect of a home-based inspiratory muscular training programme on functional capacity in patients with chronic COVID-19 after a hospital discharge: protocol for a randomised control trial (InsCOVID trial)
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Otros documentos de la autoría: Palau, Patricia; Domínguez Mafé, Eloy; Sastre, Clara; Martínez Mas, María Luz; Gonzalez, Cruz; Bondía, Elvira; Albiach, Cristina; Núñez, Julio; López, Laura
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/36080
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INVESTIGACIONMetadatos
Título
Effect of a home-based inspiratory muscular training programme on functional capacity in patients with chronic COVID-19 after a hospital discharge: protocol for a randomised control trial (InsCOVID trial)Autoría
Fecha de publicación
2022Editor
BMJ Publishing GroupISSN
2052-4439Cita bibliográfica
Palau P, Domínguez E, Sastre C, et al. Effect of a home-based inspiratory muscular training programme on functional capacity in patients with chronic COVID-19 after a hospital discharge: protocol for a randomised control trial (InsCOVID trial). BMJ Open Respiratory Research, 2022; 9: e001255. doi: 10.1136/bmjresp-2022-001255Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://bmjopenrespres.bmj.com/content/9/1/e001255Versión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
Introduction: Exercise intolerance and fatigue are the most common symptoms in patients with chronic COVID-19 after hospital discharge. Supervised exercise training programmes improve symptoms, but scarce research has ... [+]
Introduction: Exercise intolerance and fatigue are the most common symptoms in patients with chronic COVID-19 after hospital discharge. Supervised exercise training programmes improve symptoms, but scarce research has been done on home-based exercise programmes on the maximal functional capacity for discharged symptomatic COVID-19 patients. This study evaluates whether a home-based inspiratory muscle training (IMT) programme improves maximal functional capacity in chronic COVID-19 after hospital admission.
Methods and analysis: This single-centre, assessor-blinded randomised controlled trial, powered for superiority, seeks to evaluate maximal functional capacity as the primary endpoint. A total of 26 eligible patients with a previous admission for acute respiratory syndrome coronavirus 2 pneumonia (>3 months after hospital discharge) will be randomised (1:1) to receive a 12-week programme of IMT versus usual care alone. A blinded assessor will measure outcomes at baseline and after the intervention (12 weeks). An analysis of variance will be used to compare continuous outcomes among the two-intervention groups. As of 21 March 2022, eight patients have been enrolled.
Ethics and dissemination: The research ethics committee (Comité Ético de Investigación con Medicamentos de l'Hospital Clínic Universitari de València) approved the protocol following the principles of the Declaration of Helsinki and national regulations (Approval Number: 021/226). Findings will be published in peer-reviewed journals and conference publications. [-]
Publicado en
BMJ Open Respiratory Research, 2022, vol. 9, no 1Entidad financiadora
Sociedad Española de Cardiología: Investigación Clínica en Cardiología
Código del proyecto o subvención
SEC 2021
Derechos de acceso
info:eu-repo/semantics/openAccess
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