HumRes64850
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NCT05739552
Telerehabilitation in the Post-COVID-19 Patient (TRIALS)
Type of trial
Interventional
(ICTRP)
Intervention under investigation
Other: Telerehabilitation program
(ICTRP)
Disease under investigation
Post-COVID-19 Syndrome
(ICTRP)
Criteria for participation in trial
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)
Exclusion criteria
not available
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)
Exclusion criteria
not available
Trial sites
Switzerland, Italy
(ICTRP)
General Information
Politecnico di Milano
(ICTRP)
Scientific Information
Politecnico di Milano
(ICTRP)
Academic title
Telerehabilitation in the Post-COVID-19 Patient: the Italy-Switzerland Experience (ICTRP)
Trial design
Allocation: N/A. Intervention model: Sequential Assignment. Primary purpose: Supportive Care. Masking: None (Open Label). (ICTRP)
Primary and secondary end points
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)
not available
Registration date
not available
Incorporation of the first participant
not available
Secondary sponsors
Politecnico di Milano (ICTRP)
Additional contacts
Veronica Cimolin, Politecnico di Milano (ICTRP)
Secondary trial IDs
31A101 (ICTRP)
Results-Individual Participant Data (IPD)
not available
Further information on the trial
https://clinicaltrials.gov/ct2/show/NCT05739552 (ICTRP)
Results of the trial
Results summary
not available
Link to the results in the primary register
not available