Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Baylor University
With
National Institute on Aging (NIA)
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of MCI or dementia at a neurology and/or neuropsychology office visit in the BSWH Temple region, or neuropsychology office visit in the RR BSWH region within 12 months of the study contact (Specific ICD Codes outlined below).
Interest in participating in research
Able and willing to bring a legally authorized representative (spouse or medical power of attorney) to initial training session.
Able to independently consent according to the results of a structured capacity to consent interview OR is interested after going through the consent process but does not pass capacity to consent inventory AND has a legally authorized representative available to provide proxy consent.
Presence of no more than mild dementia on the basis of telephone administered cognitive screening instrument (TICS-M) \& Collateral/Informant ADL Measure
o Using the TICS-M and published normative data, all subjects must have scores that are around -1 to -2 standard deviations for demographically corrected norms (National Institute of Aging-Alzheimer's Association recommended criteria for the very mild to mild stages of Alzheimer's disease; Albert et al., 2011; McKhann et al., 2011).
Etiology of the dementia or MCI can be varied or unknown at the time of the screening criteria.
You may not be if
Presence of severe cognitive impairment defined by a TICS-M score \<-2 standard deviations from the mean.
* Serious mental illness (schizophrenia, bipolar, or depression with suicidal ideation in the last 30 days) are present and significantly contributing to the current presentation
* Uncorrected hearing loss, visual loss, or motoric dysfunction would preclude using the smartphone.
English language proficiency (whether due to English as a second language or the presence of aphasia) significantly interferes with completion of telephone screening procedures or would be clinically suspected to interfere with completion of the study process.