None listed
Conditions
Interventions
Control Intervention1: NIL: NIL
Sponsors
Nuffield department of population health
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male or Female who participated in the previous study (Project No.560) 2. Age: 30-69 (at the time of the enrolment of Project no.560)
Exclusion criteria
Exclusion criteria: 1. Unwilling to participate 2. Has a history of cough, cold, and fever 3. Unable to lie still 4. Unable to hold breath voluntarily or hear instructions 5. Unable to complete the process because of physical disabilities. 6. Pregnant women /lactating women 7. Had surgery in the last 6 weeks 8. Had a scan or x-ray in the last 2 weeks which involved taking a contrast medium
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Describe the detailed anthropometric characteristics in this Indian cohort. 2.Compare conventional measures of adiposity and body fat distribution (derived from weight, height, waist and hip circumference) with DXA-derived measurements in this population. 3.Assess the association between DXA-derived measures of body composition and with cancer and other non- communicable disease risk factors. 4.Enable comparative analyses of the associations between body composition and risk of non- communicable disease (and mediators thereof) in the ISHA cohort and UK Biobank. 5.Undertakethe optical coherence tomography (OCT) imaging to understand association of retinal thickness with cancer and non-communicable disorders. Timepoint: 3 years for enrollment and initial prevalence analysis; further follow up of minimum 10 years Typically longitudinal cohort studies does long-term follow up until all the members of cohort are diseased | — |
Secondary
| Measure | Time frame |
|---|---|
| NATimepoint: NA | — |
Countries
India
Contacts
Public ContactDr Sharayu Mhatre
Center for Cancer Epidemiology, Tata Memorial Center
Outcome results
None listed