Memory Loss Prevention

  • STATUS
    Recruiting
Updated on 30 July 2021
dementia
alzheimer's disease

Summary

All medications approved by the FDA for Alzheimer’s disease help treat the symptoms or slow down the progression of the disease. There are no treatments that address the underlying cause of the disease.

As we learn more about the brain, researchers have been better able to design research programs that target the underlying disease. Many of these studies are focusing on prevention for those at risk of developing dementia secondary to Alzheimer’s disease even before symptoms occur.

Research studies for “memory loss prevention” include those who are at increased risk of developing dementia secondary to Alzheimer’s disease due to a combination of contributing factors such as age, family history, genetic markers and brain changes found in imaging results.

This research may help to provide long-term data necessary to help us better understand progressive nature and contributing factors of Alzheimer’s disease and what can be done in the future to help find better treatments and a cure.

Description

The Memory Health Center at Summit Research conducts clinical trials for memory loss prevention:
  • Qualified participants receive all study related care, study drug, study related office visits and evaluation (often including imaging) at no cost
  • No insurance is required to participate
  • Compensation may be available
If you would like to learn more about Memory Loss Prevention research studies, please contact the Research team at 503-228-2273 or visit us at https://memoryhealthcenter.com/memory-loss-prevention/
 

Details
Condition Dementia, Alzheimer's Disease, Mild Cognitive Impairment, Memory Loss, Memory Problems
Clinical Study IdentifierTX278665
Last Modified on30 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Be 55 to 80
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  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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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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