None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: We will include all permanent residents of the selected cluster who are 60 years or above of age as participants for the trial. The participants should be able to provide written informed consent and agree to follow up for 24 months
Exclusion criteria
Exclusion criteria: We will exclude those with severe cognitive impairment (as assessed by the Dementia assessment rapid test- DART), those unable to comprehend/communicate, seriously ill/bed ridden patients and those who plan to move out of the study site during the trial period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of interest is a change in Quality-of-life scores (WHO-BREF-Odia version) between baseline & at 12, 18 & 24 months.Timepoint: 12, 18 & 24 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes in terms of self-rated health, hospitalization, emergency/out-patient visits, out-of-pocket expenditure & compliance with treatments will be assessed. The outcomes will be evaluated at the individual levels and at same time points as the primary outcomes.Timepoint: 12, 18 & 24 months | — |
Countries
India
Contacts
ICMR-RMRC, Bhubaneswar