SAMPLE Registry, Serial Alzheimer’s disease and MCI Prospective Longitudinal Evaluation

  • STATUS
    Recruiting
Updated on 15 September 2020

Summary

All candidates will be seen by a psychiatrist every 6mths, memory testing, blood test, CSF, and ( MRI/CT if not current within last 2 years} will be provided at no cost.Compensation provided. Caregiver/informant required.

Description

All candidates will be seen by a psychiatrist every 6mths, memory testing, blood test, CSF, and ( MRI/CT if not current within last 2 years} will be provided at no cost.Compensation provided. Caregiver/informant required.

Details
Condition Alzheimer's Disease, Mild Cognitive Impairment
Clinical Study IdentifierTX249211
Last Modified on15 September 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 50 yrs?
Gender: Male or Female
Do you have any of these conditions: Alzheimer's Disease or Mild Cognitive Impairment?
You could be eligible for this study if
You are 50 or older
You weigh more than 99 pounds
You have mild cognitive impairment or mild Alzheimer’s, as confirmed by pre-study testing
-You are cognitively able to give your own consent to participate in all study activities
Your life expectancy is 3 years or greater
You have a ‘study partner’—a spouse, friend, or caregiver—who would be willing to answer questions about you
You may not be eligible for this study if
You have non-Alzheimer’s dementia, including vascular dementia
You have a neurological condition, including stroke, brain tumors, thyroid disease, pernicious anemia, tertiary syphilis, nervous system infections, hydrocephalus, Huntington’s disease, Creutzfeldt-Jakob disease, or Korsakoff’s syndrome
You take a large number of medications on a regular basis
You are intoxicated at the time of study activities
You cannot have a spinal tap, for example due to using aspirin or anti-coagulant medications
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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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