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Clinical Trials in India / NCT07815730
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Development and Validation of the Indian Asthma Care Bundle for Reducing Readmission and Improving Post-hospitalisation Care After Discharge From Hospital Due to an Acute Asthma Exacerbation

NCT07815730 · tracked via the Priya Life Science India tracker
Sponsor
Ahmedabad University
Phase
N/A
Started
2026-12-01
Last updated
2026-09-11

Condition(s) studied

Asthma ExacerbationAsthma (Diagnosis)ExacerbationsHospitalisation

Investigational drug(s) / intervention(s)

Indian Asthma Care Bundle (I-ACB)

Indian Asthma Care Bundle (I-ACB): I-ACB is a structured hospital-initiated asthma care bundle (I-ACB), a contextual and India-specific post-discharge care bundle tailored for adult asthma patients hospitalised for asthma.

Study summary

The goal of this study is to assess the effectiveness of the Indian Asthma Care Bundle (I-ACB) in improving post-discharge asthma management among patients with asthma in India, specifically targeting adults and children experiencing severe asthma exacerbations.

The main questions it aims to answer are:

1. Does the I-ACB reduce the rate of hospital readmissions within 30, 60, and 90 days post-discharge?
2. How does the I-ACB impact treatment adherence, lung function, symptom control, and overall quality of life, compared to usual care?

Researchers will compare outcomes among participants receiving the I-ACB with those receiving standard asthma care (usual care) to determine whether the I-ACB improves health outcomes and reduces the need for emergency department visits.

Participants will be asked to:

* Engage in a structured asthma management program that includes education on inhaler techniques and adherence to treatment plans.
* Report their symptoms and treatment adherence regularly.
* Participate in follow-up assessments that monitor lung function and quality of life over a specified period.

The importance of this study lies in its potential to address significant gaps in asthma management in India, which currently lead to high hospitalisation rates and substantial healthcare costs. By developing a tailored care strategy, the I-ACB aims to improve health outcomes for millions of asthma patients, reducing the burden on families and healthcare systems alike, and ultimately transforming the approach to asthma care in the region.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Adults (≥ 18 years of age) participants with a doctor-diagnosed asthma * admitted to a tertiary care facility/hospital due to an acute asthma exacerbation * attended at least a primary school to read, comprehend, and write English/Hindi/local language * provide informed consent Exclusion Criteria: * a diagnosed co-pulmonary condition, such as chronic obstructive pulmonary disease, bronchiectasis, interstitial lung disease or other chronic respiratory disorders * a recent (in the past 6 months) history of hospitalisation due to influenza, pneumonia, or any respiratory tract infections * a recent (in the past 6 months) hospital admission due to a cardiologic condition or under medications such as statins, beta-blockers, blood thinners, etc. * a significant cognitive impairment * very low educational attainment (≤ primary school education) * transferred to another healthcare facility before discharge * discharged against medical advice.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Vardhman Mahavir Medical College and Safdarjung Hospital Delhi National Capital Territory of Delhi
Apollo Multispeciality Hospitals (previously Apollo Gleneagles Hospital) Kolkata West Bengal
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07815730 on ClinicalTrials.gov ↗ ← All trials in India