Indianapolis, INNCT06152614Now EnrollingIRB Ready

Cognitive Decline Clinical Trial in Indianapolis, IN

Access cutting-edge cognitive decline treatment through this clinical trial at a research site in Indianapolis. Study-provided care at no cost to qualified participants.

Sponsored by Indiana University

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Expert Care in Indianapolis

Access cognitive decline specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related cognitive decline treatment provided free

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Check if you qualify for this cognitive decline clinical trial in Indianapolis, IN

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Indianapolis

    Convenient for IN residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Indianapolis site if eligible
  4. 4Begin participation

About This Cognitive Decline Study in Indianapolis

The goal of this randomized controlled trial is to determine the impact of Mediterranean-Dash Intervention for Neurodegenerative Delay (MIND) diet and aerobic training on cognition in Black adults with high systolic blood pressure. Researchers will compare Food Delivery and Cooking PLUS Aerobic Training (FoRKS+) versus Enhanced Usual Care (EUC) to evaluate the effects on cognition. Participants will complete cognitive and cardiovascular assessments, 24-hr blood pressure monitoring, standard blood pressure measurements, weight, fingerstick for HbA1c point-of-care testing, and questionnaires. Participants may also choose to participate in an optional blood draw for DNA Repair Capacity testing as a modifiable risk factor for aging-associated diseases.

Sponsor: Indiana University

Who Can Participate

Inclusion Criteria

Fluent in English
Marion County resident
35-75 years
Self-identified non-Hispanic and Black/African-American/biracial including African-American
Systolic BP of ≥140 in prior 12 months from a primary care visit
Ability to see and read street signs (self report)
Stable housing with independent access to kitchen, including functional stove or hotplate, oven, refrigerator, and freezer (self report)
Activity independence per functional activities questionnaire (FAQ; \<3 responses of "Require Assistance" and 0 responses of "Dependent")
Normal cognition per six-item screener (SIS; score of ≥ 5)
Less than 20min on usual day of moderate or vigorous physical activity
Able to exercise safely per abbreviated Exercise Assessment for You (EASY) or primary care provider clearance
Mean systolic BP of ≥130 from 3 standard BP measurements taken by research staff following standardized wait periods.

Exclusion Criteria

lives in nursing home
diagnosis of dementia or Alzheimer disease or mild cognitive impairment; Parkinson disease; brain tumor/infection/surgery (within the last 10 years with residual symptoms and/or functional loss/deficit, such as impaired learning, memory, or communication); cancer with short life expectancy, or current chemotherapy or radiation therapy; psychosis, schizophrenia, or bipolar disorder
ICD 10 code I11/hypertensive heart disease, ICD 10 code I12/hypertensive CKD, ICD 10 code I13/hypertensive heart disease and CKD, ICD 10 code I15, or ICD 10 code I16
current or past prescription of donepezil, memantine, rivastigmine, or galantamine
alcohol consumption ≥ 8 drinks per week for women, or ≥15 drinks per week for men
drug use/abuse (excluding marijuana) per EMR
moving out of area during study timeline
scheduling conflicts with intervention schedule
unwilling to use a touchscreen
unwilling to be on video conferencing
low communicative ability, functional status, or other disorders (examiner rated) that would interfere with interventions and assessments
unable to provide informed consent
participation in any lifestyle modification/weight loss program (e.g., Weight Watchers, etc.)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Indianapolis?

Yes, this clinical trial (NCT06152614) has an active research site in Indianapolis, IN that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Cognitive Decline Treatment Options in Indianapolis, IN

If you're searching for cognitive decline treatment options in Indianapolis, IN, this clinical trial (NCT06152614) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Indianapolis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced cognitive decline specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all cognitive decline clinical trials near you to find additional studies recruiting in your area.

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