Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06542458
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-05
Brief Title:
Under-Represented Communities Diagnosed With SCD or MCI Through Tele-Cog
Sponsor:
None
Organization:
None
Study Overview
Official Title:
A Cohort Study of Older Adults From Under-resourcedUnder-represented Communities Diagnosed With Subjective Cognitive Decline SCD or Mild Cognitive Disorder MCI Through Standard of Care Tele-Cog Visits Tele-Cog
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Overall this studys primary aim is to establish a prospective longitudinal observational cohort study of older adults at risk for dementia from under-resourcedunderrepresented communities More specifically older adults diagnosed with subjective cognitive decline SCD or Mild Cognitive Impairment MCI during clinical care offered via the Tele-Cog clinic would be recruited for more comprehensive data collection to characterize the clinical presentation and course of illness over multiple timepoints spread out longitudinally
Detailed Description:
Clinical data obtained as part of standard of care will be collected from the medical record including clinical diagnosis cognitive and other neuropsychological test scores lab results neuroimaging data etc and additional data neuropsychological test batteries and clinical questionnaires if not already obtained would be obtained at research study visits
Participants will be asked to participate in annual research visits for up to 5 years
Participants will be asked to participate in annual research visits for up to 5 years
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None