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Individuals in IT-based intervention will be enrolled via the emergency ward where all personal information is available.
Participants who wear the accelerometer for at least 4 days (≥ 10 hours each day), are willing to accept randomized group assignment, and remain committed to working through potential scheduling conflicts and other logistical issues that may come up during the intervention will be enrolled in the study and subsequently scheduled for baseline measures and randomization procedures.
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Participants allocated in the intervention group will be enrolled in three weekly non-consecutive training sessions for 8 weeks.
Village doctors in the intervention arm will be enrolled and will be given a smart phone with pre-installed app and asked to use the app to manage immunization in their catchment areas.
Women will be enrolled during four enrollment periods.
Recruited patients will be enrolled in the intervention arms by the principal investigator and receive treatment accordingly.
Approximately 674 patients will be enrolled to either the intervention or control group.
Within these eight districts 50 NPCs will be selected and will be enrolled on the training programme (the intervention).
210 patients will be enrolled and randomized to either the LIFE intervention or a standard of care control group, which consists of two dietitian-led diabetes self-management classes.
In a cluster randomized controlled trial, with the general practice as the unit of randomization, 1281 participants from 25 general practices will be enrolled in each condition to compare the intervention with usual care.
Patients And Intervention Two hundred patients with atrial fibrillation >2 days' duration requiring early chemical or electric cardioversion will be enrolled.
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