Standardization of assessments or data capture (including historical use of a method in the research group)
|
“A systematic approach based on pharmacovigilance procedures developed by our collaborators”
|
x
|
x
|
x
|
|
“We are used to that”
|
Specificity of data sought (seeking information about particular adverse events, malaria symptoms or drugs)
|
“We wanted to find out about specific symptoms and adverse effects”
|
x
|
x
|
x
|
|
“The named drug questions targeted drugs of special interest”
|
Comprehensiveness of data sought (participant guidance, report clarification, overcoming barriers to reporting such as poor recall or ability to name medicines)
|
“To provide a clear understanding about what investigators are looking for and to be sure they capture all complaints from study participants”
|
|
x
|
x
|
x
|
“To get more information which may have been missed during the initial interview”
|
Avoidance of suggestion
|
“Keeping questions open and not leading so that only events significant to the patient are reported”
|
x
|
|
x
|
|
Feasibility
|
“A simple screen [as the] main focus of the study was not safety/tolerability”
|
x
|
x
|
x
|
|
“Appears simple and not complex”
|
Understand participants’ perceptions about health
|
“[To] know if [symptoms] are related to chronic disease or traditional belief” |
|
x |
x |
|