Effectiveness of Cognitive Training in Older and Younger Adults

Description

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.

Conditions

Cognitive Change

Study Overview

Study Details

Study overview

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.

Examining the Effectiveness of Cognitive Training

Effectiveness of Cognitive Training in Older and Younger Adults

Condition
Cognitive Change
Intervention / Treatment

-

Contacts and Locations

Riverside

University of California, Riverside, Riverside, California, United States, 92521

Boston

Northeastern University, Boston, Massachusetts, United States, 02115

Madison

University of Wisconsin - Madison, Madison, Wisconsin, United States, 53706

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Self-reported normal or corrected-to-normal vision
  • * No known neurological impairments
  • * Abnormal visual acuity prohibitive of training
  • * History of seizures, focal brain lesion, or head injury with loss of consciousness in the past year
  • * Physical handicap (motor or perceptual) that would impede training procedures
  • * Medical illness requiring treatment during the study timeline
  • * Social, educational or economic hardship prohibitive to training schedule
  • * Concurrent enrollment in other cognitive training studies
  • * History of major psychiatric illness, including psychosis, bipolar disorder, alcohol or substance abuse, recent bereavement
  • * Score of 5 or more (i.e. presence of mild, moderate, or severe depression) on the Patient Health Screening Questionnaire (PHQ-9 Depression Screening); any participants reporting suicidal tendencies will be immediately referred to the site-specific Emergency Psychiatry Services (24-hour availability), and those with high depressive symptoms will be referred to their personal physician
  • * Current alcohol consumption that exceeds 14 drinks per week
  • * Illicit drug use
  • * Plans to travel out of the area for more than 1 week during the intervention period
  • * Residence too far from the testing site, which would prevent attending the testing sessions (\> 60 miles)
  • * 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).
  • * Diagnosis of dementia or other neurological disease, including mild cognitive impairment (MCI)
  • * Score \< 26 (out of 30) on the Mini Mental State Exam (MMSE)
  • * Score \< 18 (out of 22) on the Telephone Montreal Cognitive Assessment (T-MoCA).

Ages Eligible for Study

18 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of Wisconsin, Madison,

Aaron R. Seitz, PhD, PRINCIPAL_INVESTIGATOR, University of California, Riverside

Susanne M. Jaeggi, PhD, PRINCIPAL_INVESTIGATOR, Northeastern University

Study Record Dates

2028-01