Enhancing Consent for Alzheimer's Research (BWP-AD)
Alzheimer Disease
About this trial
This is an interventional other trial for Alzheimer Disease focused on measuring computer assisted instruction, decision making, educational resource design /development, executive function
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of mild to moderate possible or probable AD or demographically comparable healthy comparison subjects
- Fluency in English
- 50 yrs and older
- Informed written consent (or written assent with consent from legally authorized representative)
Exclusion Criteria:
- Diagnosis of Lewy Body Dementia or Mild Cognitive Impairment
- MMSE less than 15
- Physical or medical conditions that preclude participants from completing tasks
- Healthy comparison volunteers if they have a known neurologic or psychiatric condition that could impair neurocognitive functioning
Sites / Locations
- Veterans Affairs San Diego Healthcare System
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Active Comparator
Active Comparator
Enhanced consent - A
Enhanced consent - B
Routine consent - A
Routine consent - B
The intervention was an enhanced consent process, including a multimedia aid for a moderate risk hypothetical protocol
The intervention was an enhanced consent process, including multimedia aide for a higher risk hypothetical protocol
This was a comparison condition - a routine consent process, including a printed consent document, for a moderate risk hypothetical protocol
This was a comparison condition - a routine consent process, including a printed consent document, for a higher risk hypothetical protocol