Disease, Infectious, Effectiveness, Respiratory Disease, Safety Issues
Conditions
Brief summary
A randomized controlled clinical trial will be carried out using inspiratory and expiratory training devices on healthy subjects recruited in social networks and university environments. The aim will be to determine the effectiveness and safety in the prevention and severity of COVID-19 disease by a respiratory training with inspiratory and expiratory devices.
Interventions
DEVICEInspiratory training device
Inspiratory training by a Power-breath device
DEVICEExpiratory training device
Expiratory training a Winner-flow device
Sponsors
Universidad Complutense de Madrid
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Healthy subjects
Exclusion criteria
* Drugs * Surgery * Neurology diseases * Rheumatic diseases * Systemic diseases * Smokers
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| COVID-19 disease diagnosis | Change from Baseline COVID-19 disease diagnosis at 8 weeks | Dichotomous categorical variable measured by yes or no responses |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| COVID-19 disease symptoms severity | Change from Baseline COVID-19 disease symptoms severity at 8 weeks | Dichotomous categorical variable measured by slight or severe responses |
| Adverse effects | Change from Baseline adverse effects at 8 weeks | Polytomous categorical variable measured by adverse effects responses |
Contacts
Primary ContactCésar Calvo Lobo, PhD
Outcome results
None listed