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Pulmonary Rehabilitation in Pneumonia patients

Optimising Pulmonary Recovery-An App Based Study On Improving Pulmonary Functions In Patients With Pneumonia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078142
Enrollment
50
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J189- Pneumonia, unspecified organism

Interventions

Intervention1: An app based study on improving pulmonary functions: Pulmonary rehabilitation in patients with pneumonia Duration:3 months Control Intervention1: NIL: NIL

Sponsors

Saveetha medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1,Adult patients (18 years and older) diagnosed with pneumonia. Patients admitted to the designated hospital for treatment of pneumonia. 2,Confirmed diagnosis of pneumonia based on clinical symptoms, radiological findings, and/or laboratory tests. 3,Willingness and ability to participate in the study, including the ability to use a smartphone or access to a caregiver who can assist with app usage. 4,Patients who are clinically stable and able to undergo 6 minutes walt test,spirometry

Exclusion criteria

Exclusion criteria: 1,Patients with pre-existing chronic lung diseases (e.g., COPD, asthma) that may confound pulmonary function test results. 2mPatients with significant comorbidities or medical conditions that may interfere with the study objectives or limit life expectancy. 3,Patients with cognitive impairments or language barriers that may hinder understanding or adherence to the app-based intervention. 4,Patients with contraindications to pulmonary function testing or unable to perform spirometry or lung volume measurements. 5,Non smoker

Design outcomes

Primary

MeasureTime frame
Evaluating the effectiveness of app based interventions against conventional methods pulmonary functions among patients recovering from pneumonia by measuring the pulmonary function test before and after pulmonary rehabilitation Timepoint: Evaluating the effectiveness of app based interventions against conventional methods pulmonary functions among patients recovering from pneumonia by measuring the pulmonary function test before and after pulmonary rehabilitation from the date of discharge After 3 months i.e., 12 weeks of duration

Secondary

MeasureTime frame
Symptoms evaluated by Borgs dyspnea scale,QOL improvement after the pulmonary rehabilitationTimepoint: 3 months

Countries

India

Contacts

Public ContactDR RENUGADEVI V

Saveetha Medical College and Hospital

drguna59@gmail.com09884398420

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026