Initial consent processes
Having to seek either full consent or nothing—no assent process
Parents not wanting all of the information or not listening
Parents put off by blood samples
What to do where a mother consents and then someone else wants her to change her mind—what if the mother still wants the child to be in the study
Consenting controls
Ending the study
Ending the study when a child has died and verbal autopsies (VAs)
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Some elements of the study emotionally challenging
Blood sampling: Painful to hear children cry and mothers upset
Socioeconomic status, nutrition and mental health questions: Because of the questions that have to be asked, getting to hear about, for example, how hungry families are and about high levels of depression
Levels of compensation of families:
‘Small’ differences between studies in what is given/paid for a routine study clinic—for example, if a banana is given, and 350/=vs 300/=
Lack of clarity on lunch provision for hospital visits over lunch and whether food/fares can be given to others accompanying the mother to hospital
Home visits for research costing household members money (cannot earn) or preventing household (HH) tasks, especially where take longer than expected
Why cannot we give more to people who earn more, otherwise they will drop out?
Referral of inadequate perceived quality or unlikely to be taken up
Where the types of clinical needs are way beyond what’s easily desirable, available or affordable to families
Where does a referral end? For example, depressed mother
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Ability to help as fellow community members
Attending funerals
Levels of compensation of staff for emergency costs incurred
Other
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