About this trial
The ICRAG-2 project aims to assess the impact, cost-effectiveness, and sustainability of a low-cost, multipronged intervention package to reduce cardiovascular disease (CVD) burden in India. Given the high CVD mortality rate in India, this study addresses the urgent need for scalable, evidence-based solutions. The project will unfold in three steps: first, formative research including systematic reviews, cross-sectional studies, and qualitative studies will identify key barriers, facilitators, and refine interventions. Next, a matched-pair cluster randomized controlled trial (CRCT) across 26 clusters will evaluate the intervention's impact on CVD outcomes over three years, focusing on therapeutic lifestyle changes, fixed-dose medications, and task-sharing with non-physician health workers. Finally, the project will engage stakeholders through policy dialogues to support potential national-scale implementation. This trial offers a promising model to reduce CVD incidence through customized, sustainable interventions targeting patients, providers, and the health system.
Eligibility criteria
Qualifiers
None
Disqualifiers
Severe cognitive impairment of any aetiology and have no reliable caregivers.
Medical conditions with a survival prognosis of less than 12 months.
Unable to follow-up for the study period
Trial design
Treatments tested in this trial
- FDC and TLC and medication adherance
- Patients will Enhanced Usual Care (EUC)
Treatment groups
Sponsors and collaborators
St. John's Research Institute
Lead sponsor
Assam Medical College, Dibrugarh, India
Collaborator
SRM Medical College Hospital & Research Centre
Collaborator
Jawaharlal Institute of Postgraduate Medical Education & Research
Collaborator
Indian Council of Medical Research
Collaborator
All India Institute of Medical Sciences, Bhopal
Collaborator