HumRes64850
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NCT05739552
Telerehabilitation in the Post-COVID-19 Patient (TRIALS)
Studientyp
Interventional
(ICTRP)
Untersuchte Intervention
Other: Telerehabilitation program
(ICTRP)
Untersuchte Krankheit(en)
Post-COVID-19 Syndrome
(ICTRP)
Kriterien zur Teilnahme
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)
Ausschlusskriterien
nicht verfügbar
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)
Ausschlusskriterien
nicht verfügbar
Studienstandort
Schweiz, Italien
(ICTRP)
Allgemeine Auskünfte
Politecnico di Milano
(ICTRP)
Wissenschaftliche Auskünfte
Politecnico di Milano
(ICTRP)
Wissenschaftlicher Titel
Telerehabilitation in the Post-COVID-19 Patient: the Italy-Switzerland Experience (ICTRP)
Studiendesign
Allocation: N/A. Intervention model: Sequential Assignment. Primary purpose: Supportive Care. Masking: None (Open Label). (ICTRP)
Primäre und sekundäre Endpunkte
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)
nicht verfügbar
Registrierungsdatum
nicht verfügbar
Einschluss des ersten Teilnehmers
nicht verfügbar
Sekundäre Sponsoren
Politecnico di Milano (ICTRP)
Weitere Kontakte
Veronica Cimolin, Politecnico di Milano (ICTRP)
Sekundäre IDs
31A101 (ICTRP)
Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar
Weitere Informationen zur Studie
https://clinicaltrials.gov/ct2/show/NCT05739552 (ICTRP)
Ergebnisse der Studie
Zusammenfassung der Ergebnisse
nicht verfügbar
Link zu den Ergebnissen im Primärregister
nicht verfügbar