None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The participant is willing to sign IEC approved Informed consent will be recruited meet the following criteria 1.Adults aged 25-65 years. 2.Representing NDW, SW, and NSW. 3.No history of sleep disorders or psychiatric conditions.
Exclusion criteria
Exclusion criteria: 1.Individuals with type 1 diabetes and secondary diabetes. 2.Pregnant individuals.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The expected outcomes include actionable insights into designing personalized interventions that optimize circadian alignment, potentially improving metabolic outcomes in night shift workers with specific disorders.Timepoint: From baseline to end of study at year1, year 2, year3 and year 4 | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the association between chronotype at morningness to eveningness preference and the severity of metabolic parameters e.g., insulin resistance, BMI, glycaemic variability in shift workers. Helps stratify participants based on intrinsic biological clock tendencies and tailor interventions more precisely. To evaluate the feasibility, adherence, and participant satisfaction with personalized lifestyle interventions aligned with circadian patterns over a 6-month follow-up period. To develop and validate a composite Circadian Disruption Risk Score integrating actigraphy data, gene expression profiles, and metabolic biomarkers for predictive risk stratification in night shift workers.Timepoint: From baseline to end of study at year1, year 2, year3 and year 4 | — |
Countries
India
Contacts
Government Institute of Medical Sciences (GIMS)