Ben Littenberg, Mariana Wingood,
Justine Dee, Levi, Bonnell, Juvena Hitt, CvE
1. Poster
presentations
a.
Choose 3-4 key items from each trial
b. Match
to the PRECIS diagram
c.
Add conclusions at the bottom
d. Left
side: methods, goal, objectives...
e.
Why NAPCRG
i.
PC studies
ii.
Pragmatic
iii.
Complex
iv.
Here’s what we learned
1. Generalizable
(externally valid) vs internally valid – essentially true of all science
a.
Pragmatic trials are different by degree
b. Are
they more complex – i.e. unpredictable
c.
The volume of challenges
i.
Data sampling frame / recruitment
ii.
Data collection
iii.
Intervention
d. Good
research is hard; what makes pragmatic trials hard magnifies these issues: high
levels of external/internal validity with complex interventions on complex
population. Complexity exists in all science; pragmatic trials bite them
off all at once, rather than trying them one at a time. We are understanding
the world of people, necessarily complex.
2. Flexibility
3. Team
work
2. Content
a.
Too dense
i.
Simplify to “this is the challenge” and “this is how
addressed”
b. Implementation
issue: changed to empower sites to modify the intervention
c.
Outcomes: challenge in the clinic to collect outcomes
data; sites empowered (PREPARE)
3. Three
worlds of CJ Peek – to be distributed
4. Next
week: open
a.
Following week: Jen’s discussion on Oct 10
It look like the paper Connie was referencing is actually a book chapter
https://link.springer.com/chapter/10.1007/978-0-387-76894-6_3
I also found some lecture slides given by CJ Peek on the topic
http://www.cbhc.org/news/wp-content/uploads/2010/07/Session-1003.pdf
https://link.springer.com/chapter/10.1007/978-0-387-76894-6_3
I also found some lecture slides given by CJ Peek on the topic
http://www.cbhc.org/news/wp-content/uploads/2010/07/Session-1003.pdf
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