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2. A small sample of client participants and service providers will be interviewed to assess establishment of the new pathway within routine care.
At all follow-up visits, participants in both study groups will be interviewed to assess adverse events, changes in insulin regimen or in non-insulin medications, including supplements and vitamins, and diabetes complications.
In brief, the following types of data will be collected in the respective samples: Sample 1: Caregivers and teachers will complete questionnaires while caregivers and children will be interviewed to assess maltreatment experiences, social support, emotion regulation (see Tables 1 and 2).
After randomization (visit 1) at visits 2 to 5, both study groups, intervention and control, will be interviewed to assess and document adverse events including severe hypoglycemia requiring assistance, hospitalization, any changes in non-insulin medications, supplements and vitamins from previous visit.
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In this research adults were interviewed to assess whether they promote children's participation in DRR.
In addition, the staff in the Department of Civil Affairs and the Department of Medical Insurance was interviewed to assess health equity in the reform.
A convenience sample of 30 men and 30 women who had CABG surgery at least 1 year earlier and were enrolled in a follow-up program through a cardiovascular surgeon's office were interviewed to assess coronary artery disease risk.
Health workers (medical assistants) were interviewed to assess their capacity in diagnosis and treatment of leprosy.
Finally, all participants were interviewed to assess their knowledge of patient interview and examine whether the groups were well-balanced.
The staff responsible for the units were interviewed to assess whether the infection control measures were being followed.
One month prior to the expected date of delivery, the women were interviewed to assess retention of knowledge.
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CEO of Professional Science Editing for Scientists @ prosciediting.com