1. System |
AD diagnostic pathway |
linking up systems with other sites |
|
poor record keeping and quality of information (local) |
establish links with other services and recruitment avenues |
|
research not embedded in culture of AD care |
make research part of standard treatment options |
|
lack of/inaccurate information on national database |
multiple staff members using national database |
|
resources needed to use the national database |
|
self-selected nature of patients on national database |
2. Healthcare Professionals |
gate-keeping |
personal knowledge/direct contact |
|
lack of connection with other sites |
good links with other researchers/sites |
|
|
staff training |
3. Patient and companions |
requirement for research partner/companion |
presentation of clear, simple and concise information |
|
research partner/companion acting as a gate-keeper |
follow-up with patient |
|
overly complex/unnecessarily detailed language/materials |
prior patient involvement in research |
|
insufficient information on key topics |
patient belief in the trial and its benefits |
|
concerns for clinical condition and prolonged participation |
|
preference for active arm |