Effectiveness of Cognitive Training in Older and Younger Adults
Examining the Effectiveness of Cognitive Training
University of Wisconsin, Madison
1,600 participants
Oct 1, 2024
INTERVENTIONAL
Conditions
Summary
The proposed study will enroll 1600 participants to examine the effectiveness of cognitive training. Participants will be randomized into different experimental groups and can expect to participate for up to 15 hours of research over 4 to 8 weeks.
Eligibility
Inclusion Criteria3
- Self-reported normal or corrected-to-normal vision
- No known neurological impairments
- Age within inclusion range (18-30 Years for Younger Adults and 60-85 Years for Older Adults)
Exclusion Criteria5
- Physical handicap (motor or perceptual) that would impede training procedures
- Concurrent enrollment in other cognitive training studies
- Not being proficient enough in English that would prevent following and understanding all instructions and completing all testing sessions (typically, participants would need to have learned English before age 11; there might be some exceptions that will be decided on a case-by-case basis).
- Unable to adhere to training schedule
- \- Score < 17 (out of 22) on the Telephone Montreal Cognitive Assessment (T-MoCA).
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Interventions
Seven sessions (\~45-75 minutes) of cognitive tasks in the lab. Participants asked to view visual stimuli (such as black and white lines, letters, simple shapes like triangles, circles, and squares) presented on a computer or television screen and/or listen to auditory stimuli (such as pure tones) presented via headphone or speakers and asked to make simple judgements.
Two sets of 10 sessions (\~20 minutes) of cognitive tasks either at home or in the lab. Participants asked to view visual stimuli (such as black and white lines, letters, simple shapes like triangles, circles, and squares) presented on a computer or television screen and/or listen to auditory stimuli (such as pure tones) presented via headphone or speakers and asked to make simple judgements.
Locations(3)
View Full Details on ClinicalTrials.gov
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NCT06375681