Bloomington, INNCT06403345Now EnrollingIRB Ready

Mild Cognitive Impairment Clinical Trial in Bloomington, IN

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

Sponsored by Indiana University

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Expert Care in Bloomington

Access mild cognitive impairment specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related mild cognitive impairment treatment provided free

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Check if you qualify for this mild cognitive impairment clinical trial in Bloomington, 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 Bloomington

    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 Bloomington site if eligible
  4. 4Begin participation

About This Mild Cognitive Impairment Study in Bloomington

The purpose of this study is to test the Green Activity Program that was designed with people living with memory challenges and their study partners to see if it can be done and if they enjoy the program. "Green activities" are nature activities that the person enjoys and can be done with other people or pets. For example, dog walking, hiking, outdoor yoga, and gardening are all green activities. The purpose of the program is to help people living with memory challenges participate in nature activities they enjoy. The goal of the program is to help people stay active and improve their health and well-being.

Sponsor: Indiana University

Who Can Participate

Inclusion Criteria

45 years or older
Has memory challenges or difficulties thinking
Have access and ability to respond to the telephone (mobile or landline) Study partner
18 years or older
Speaks Spanish or English
Identified by the PLMC as a person they feel comfortable with who they would like to join them in the study. The study partner's participation is based on level of support needed for the PLMC. Outdoor activity professionals
18 years or older
at least 1 year experience providing outdoor activities

Exclusion Criteria

Participants living with memory challenges will be excluded if they do not meet inclusion criteria or if they indicate any of the following on the 2023 Physical Activity Readiness Questionnaire + (PAR-Q+) :
Heart failure or, difficulty controlling Coronary Artery Disease, Diagnosed Abnormality of Heart Rhythm, or other cardiovascular condition.
If they report difficulty controlling CAD, Diagnosed abnormality of heart rhythm they will be excluded.
If they endorse a diagnosis of heart failure, AND report symptoms greater than NYHA Functional Classification Stage I: "No limitation of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation or shortness of breath," they will be excluded. Research assistants will be trained to ask about these symptoms during usual activities of daily living.
If their doctor has told them not to participate in physical activity due to their heart condition or another medical condition, they will be excluded.
Cancer and are in an active cycle of infusion chemotherapy or daily radiation treatments.
People with cancer whose treatment regimen does not impact their day to day routines (e.g.-oral chemotherapy agents) may participate. Research assistants will be trained to ask about the impact of cancer and cancer care on day to day activities and physical activity.
If their doctor has told them not to participate in physical activity due to their cancer or cancer treatment or another medical condition, they will be excluded.
Experienced a black out, fainted, or lost consciousness as a result of a head injury in the past 12 months.
Often experienced signs and symptoms of low blood sugar (hypoglycemia) following exercise and/or daily activities.
2 or more hospitalizations in 6 months

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 Bloomington?

Yes, this clinical trial (NCT06403345) has an active research site in Bloomington, 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.

Mild Cognitive Impairment Treatment Options in Bloomington, IN

If you're searching for mild cognitive impairment treatment options in Bloomington, IN, this clinical trial (NCT06403345) 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 Bloomington research site is actively enrolling participants for this clinical trial. You'll receive care from experienced mild cognitive impairment 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 mild cognitive impairment clinical trials near you to find additional studies recruiting in your area.

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