Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified
Conditions
Interventions
Intervention1: Integrated Yoga-Pulmonary rehabilitation program delivered through a web-based application: Intervention: Non-pharmacological intervention, pulmonary rehabilitation integrated that incl
Sponsors
University of Leicester
Eligibility
Inclusion criteria
Inclusion criteria: Patients - The physician diagnosed or spirometry confirmed chronic obstructive pulmonary disease Should have access to any of the electronic devices like smart phones, tablets, computers or laptops of their own or their family members or friends so as to be able to use the web-app Ability to comprehend verbal and/or written information in Marathi or Hindi or English
Exclusion criteria
Exclusion criteria: Co-morbidities, significant cardio-vascular, hepatic, renal, neurological, orthopaedic, cognitive impairments, neoplastic diseases or recent surgery that may hamper the participation of the patient and outcome of the program Potential or eligible participants not willing to participate in study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Since this is a feasibility trial, following non-clinical outcome measures will be documented and analyzed 1. Number of participants identified, approached, consented, randomized and completed 2. Performance of participants 3. Record of patient login, accessibility and adherence and other app analytics 4. Feasibility and appropriateness of using the clinical outcome measuresTimepoint: Baseline, at 8 weeks and 12 weeks which include 6 visits along with patient initiated or required visits | — |
Secondary
| Measure | Time frame |
|---|---|
| clinical outcome measures are based on a standard international data set for pulmonary rehabilitation. Considering the risk of contagion during any surge in the covid-19 pandemic, we will conduct only remotely measurable outcomes. Medical screening, muscle strength testing, endurance and functional capacity testing, spirometry and impulse oscillometryTimepoint: Baseline, at 8 weeks and 12 weeks | — |
Countries
India
Contacts
Public ContactDr Sundeep Salvi
Symbiosis Medical College for women and Symbiosis University Hospital and Research centre
Outcome results
None listed