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. Author manuscript; available in PMC: 2023 Jun 30.
Published in final edited form as: Contemp Clin Trials. 2022 Oct 28;123:106978. doi: 10.1016/j.cct.2022.106978

Table 1:

Trial Inclusion and Exclusion Criteria

Inclusion
 Be age 65 or older at time of consent
 Have the ability to speak and understand English or Spanish
 Report adequate sensorimotor capacity to perform the computer exercises
 Report adequate visual capacity to read from a computer screen at a typical viewing distance
 Show adequate auditory capacity to understand conversational speech
 Show adequate motor capacity to touch a computer screen or control a computer mouse
 Have no evidence of mild cognitive impairment (MCI) or dementia at baseline, as assessed by education adjusted Montreal Cognitive Assessment score >=26
 Have adequate mental health (no self-reported diagnosis or mental illness that would interfere with ability to comply with study procedures or benefit from intervention)
 Wiling to complete all study activities
 Ability to understand study procedures and comply with them for the length of the study
Exclusion
 Currently enrolled in another randomized clinical trial, or treatment trial, or another research study that assesses cognition
 Previous participation in a cognitive training study
 Self-reported vision, hearing, or motor difficulties that would interfere with the ability to complete the study interventions
 Self-reported diagnosis of mild cognitive impairment, dementia, stroke, traumatic brain injury, brain tumor, or a neurological disorder that affects cognition or would interfere with the ability to benefit from the study intervention (e.g., Parkinson disease, multiple sclerosis), or any other unstable medical condition that is predisposing to imminent cognitive or functional decline (e.g., congestive heart failure, chronic obstructive pulmonary disorder dependent on oxygen, or undergoing chemotherapy or radiation)
 Self-reported use of medications typically prescribed for dementia such as Namenda, Memantine, Namzaric, Donepezil, Aricept, Rivastigmine, Exelon, Razadyne, Galantamine, Reminyl, Aduhelm or Aducanumab.
 Completion of 10 or more hours of a computerized cognitive training program in the last 5 years such as Lumosity, Posit Science Brain Fitness, InSight or Brain HQ, Listening and Communication Enhancement (LACE), CogMed, CogniFit, Happy Neuron, Elevate, or Dakim
 Severe depressive symptoms (GDS short form score >=5)