HumRes64850
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NCT05739552
Telerehabilitation in the Post-COVID-19 Patient (TRIALS)
Tipo di studio
Interventional
(ICTRP)
Intervento studiato
Other: Telerehabilitation program
(ICTRP)
Malattie studiate
Post-COVID-19 Syndrome
(ICTRP)
Criteri di partecipazione
Gender: All
Maximum age: N/A
Minimum age: 18 Years
Inclusion Criteria:
- Adult patients admitted to a rehabilitation facility for functional recovery in
disabling motor and/or respiratory outcomes of severe acute respiratory syndrome
COronaVirus 2 (SARS-CoV2) infection and residing in cross-border regions with a low
density of rehabilitation offerings.
Exclusion Criteria:
- Psychiatric disorders/cognitive impairments that do not allow proper use of tablets
and breathing training devices. (ICTRP)
Criteri di esclusione
non disponibile
Gender: All
Maximum age: N/A
Minimum age: 18 Years
Inclusion Criteria:
- Adult patients admitted to a rehabilitation facility for functional recovery in
disabling motor and/or respiratory outcomes of severe acute respiratory syndrome
COronaVirus 2 (SARS-CoV2) infection and residing in cross-border regions with a low
density of rehabilitation offerings.
Exclusion Criteria:
- Psychiatric disorders/cognitive impairments that do not allow proper use of tablets
and breathing training devices. (ICTRP)
Criteri di esclusione
non disponibile
Luogo dello studio
Svizzera, Italia
(ICTRP)
Informazioni generali
Politecnico di Milano
(ICTRP)
Informazioni scientifiche
Politecnico di Milano
(ICTRP)
Titolo accademico
Telerehabilitation in the Post-COVID-19 Patient: the Italy-Switzerland Experience (ICTRP)
Disegno dello studio
Allocation: N/A. Intervention model: Sequential Assignment. Primary purpose: Supportive Care. Masking: None (Open Label). (ICTRP)
Endpoint primari e secondari
Change from baseline aerobic endurance.;Change from baseline balance and functional mobility.;Change from baseline isometric strength.;Change from baseline in several respiratory measures.;Change from baseline in the pulmonary function test. (ICTRP)
non disponibile
Data di registrazione
non disponibile
Inclusione del primo partecipante
non disponibile
Sponsor secondari
Politecnico di Milano (ICTRP)
Contatti aggiuntivi
Veronica Cimolin, Politecnico di Milano (ICTRP)
ID secondari
31A101 (ICTRP)
Risultati-Dati individuali dei partecipanti
non disponibile
Ulteriori informazioni sullo studio
https://clinicaltrials.gov/ct2/show/NCT05739552 (ICTRP)
Risultati dello studio
Riepilogo dei risultati
non disponibile
Link ai risultati nel registro primario
non disponibile