Recruiting NA Cognitive Impairment

New treatment option for Cognitive Impairment

Official title Impact of a Multimodal Lifestyle Intervention on Dementia Risk Factors and Attitude Related to Dementia Risk: A Logistical Pilot Study

ClinicalTrials.gov ID: NCT07146412

What this study is testing

What it's testing
Many individuals develop dementia, and dementia has multiple causes, yet we currently have limited treatment options. A critical observation of the effectiveness of the available dementia treatments is that they tend to be more effective when started early.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 65 to 75. Healthy volunteers may be eligible.

You may be able to join if

  • Adults 65-75 years of age at enrollment with at least one self-reported 1st-degree relative who had or has any kind of dementia
  • Montreal Cognitive Assessment (MoCA) score \> 24 at initial enrollment
  • Able and willing to comprehend and sign the informed consent document
  • Able and willing to perform required physical performance tests
  • Able and willing to provide the study's minimum samples

You likely can't join if

  • A diagnosis of cognitive impairment of any kind, including Alzheimer's disease, mild cognitive impairment, or any other diagnosis of dementia
  • If a subject is found to have cognitive impairment at initial enrollment (Montreal Cognitive Assessment (MoCA) score\<25), they will be excluded from...
  • Self-reported pregnancy
  • Children under 19 years of age
  • Individuals not fluent in written and spoken English
  • Self-reported chronic or end-stage disease that would interfere with their participation in the study
See the full eligibility criteria
Who can join
  • Adults 65-75 years of age at enrollment with at least one self-reported 1st-degree relative who had or has any kind of dementia
  • Montreal Cognitive Assessment (MoCA) score \> 24 at initial enrollment
  • Able and willing to comprehend and sign the informed consent document
  • Able and willing to perform required physical performance tests
  • Able and willing to provide the study's minimum samples
  • Able and willing to conduct the study's minimum procedures
  • Able and willing to complete surveys, cognitive assessments, and questionnaires in English only
  • Has or has ready access to a PC, tablet, or smartphone with an internet connection required for procedures that they consent to
What rules you out
  • A diagnosis of cognitive impairment of any kind, including Alzheimer's disease, mild cognitive impairment, or any other diagnosis of dementia
  • If a subject is found to have cognitive impairment at initial enrollment (Montreal Cognitive Assessment (MoCA) score\<25), they will be excluded from the study
  • Self-reported pregnancy
  • Children under 19 years of age
  • Individuals not fluent in written and spoken English
  • Self-reported chronic or end-stage disease that would interfere with their participation in the study
  • Hospitalization for any reason in the past 3 months
  • Severe hearing and visual impairment that would interfere with the ability to complete study measures
  • Any other vulnerable subject at the time of enrollment as specified above

The study team makes the final eligibility decision.

Where it's taking place

  • Huntsville, Alabama, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65 years to 75 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Huntsville, Alabama, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.