Effectiveness of spirometry and neurophysiological facilitation technique to reduce the level of dyspnea in post covid-19 patient-A randomized controlled trial
Not Applicable
- Conditions
- Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhereHealth Condition 2: B968- Other specified bacterial agents as the cause of diseases classified elsewhereHealth Condition 3: J988- Other specified respiratory disordersHealth Condition 4: F- Physical Rehabilitation and Diagnostic Audiology
- Registration Number
- CTRI/2021/03/032135
- Lead Sponsor
- Patel Preet Sureshbhai
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who recovered from COVID-19
According to modified borg scale patient with score greater than or equal 2 to 10
Between period of 8-12 week after recovering from COVID-19
Exclusion Criteria
Geriatric age group
According to modified borg dyspnea scale patients with score 0 to 1
Patients with other disorder and diseases
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modified Borg Scale <br/ ><br>6-Minutes walk testTimepoint: 3 Weeks
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI