Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 5:05 AM
Ignite Modification Date: 2025-12-25 @ 5:05 AM
NCT ID: NCT05845918
Eligibility Criteria: Inclusion Criteria: * Age: 50 years or older * Fluency in English * African American or White * MCI will be defined as subjective memory complaints with a Montreal Cognitive Assessment (MoCA) 19- 25 * Prior diagnosis of MCI * Participants would be sedentary at baseline (self-report of \<30 minutes of structured physical activity \<3 times per week in the last 6 months) and have poor Mediterranean-Dietary Approaches to Stop Hypertension (DASH) Intervention for Neurodegenerative Delay (MIND) diet scores (using the MIND diet screener) Exclusion Criteria: * Dementia diagnosis or reversible causes of dementia (e.g., if the patient has hypothyroidism or low vitamin B12 that is contributing to the subject's cognitive impairment) * Active medical or psychiatric diseases that in the judgment of the investigator would affect the safety of the subject or scientific integrity of the study (e.g., actively manic patient) * Uncontrolled medical conditions, such as congestive heart failure, reflected by poor exercise tolerance and shortness of breath * Any physical ailment, such as stroke with residual impairment, that is a barrier to performing study procedures and attending sessions * History of brain lesions, stroke, or major head trauma in the past year * Those who are unable to demonstrate that they understood the details of the study (i.e., lack of decisional- capacity to consent) or linguistic limitations * Pregnant women, prisoners, and adults unable to consent
Healthy Volunteers: False
Sex: ALL
Minimum Age: 50 Years
Study: NCT05845918
Study Brief:
Protocol Section: NCT05845918