Respiratory Physiotherapy and Neurorehabilitation in Patients With Post-covid19 Sequelae.
- Conditions
- COVID-19 Pandemic
- Interventions
- Other: respiratory treatment
- Registration Number
- NCT05195099
- Lead Sponsor
- Universidad Católica de Ávila
- Brief Summary
The objectives are to reduce dyspnoea, increase exertional capacity, increase vital capacity and respiratory muscle strength.
vital capacity and respiratory muscle strength. In addition to increasing the sensibility of smell and taste, observing if there is a relationship between the decrease of these senses with the senses with appetite and whether appetite has normalised in post-SARS-CoV-2 patients. It is a randomised and blinded experimental study with a control group where the sample recruited will be 30 patients, with a range of of 30 patients, with an age range of 19-42 years, where they carried out an assessment of spirometry, modified Borg dyspnoea scales and modified Medical Research Council (MMRC), Singapure (MMRC), Singapore Smell and Taste Questionnaire (SSTQ) and weekly smell and taste questionnaire.
taste questionnaire.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 200
- age range between 18 and 42 years.
- patients with respiratory sequelae post Covid-19.
- patients with smell and taste sequelae post Covid-19.
- Under 18 years old.
- Over 42 years old.
- Patients not diagnosed with Covid-19 (PCR positive).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description respiratory treatment respiratory treatment - control group respiratory treatment -
- Primary Outcome Measures
Name Time Method smell and taste 1 week smell and taste questionnaire, maximum score (maximum capacity) 40 points. 0 minimum
assessment of spirometry. 1 year modified Borg dyspnoea scales (0, minimum to 10 maximum rated numerical score used to measure dyspnea as reported by the patient during submaximal exercise and is routinely administered during six-minute walk testing)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Universidad Católica de Ávila
🇪🇸Ávila, Spain