Web-based rehabilitation program for people living with chronic obstrutive lung disease in India
Phase 2
- Conditions
- Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified
- Registration Number
- CTRI/2021/11/037969
- Lead Sponsor
- niversity of Leicester
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Since this is a feasibility trial, following non-clinical outcome measures will be documented and analyzed <br/ ><br>1. Number of participants identified, approached, consented, randomized and completed <br/ ><br>2. Performance of participants <br/ ><br>3. Record of patient login, accessibility and adherence and other app analytics <br/ ><br>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 Outcome Measures
Name Time Method clinical outcome measures are based on a standard international data set for pulmonary rehabilitation. Considering the risk of contagion during any surge in <br/ ><br>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