Moderators and Mediators of Perceptual Learning (NCT05894967)
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a research study about how training can impact performance on cognitive tasks. Participants are between 18 and 30 and 60 to 85 years of age, have normal (or corrected to normal) vision, and have no neurological conditions that would preclude their ability to complete computerized cognitive tasks. Up to 1140 participants will be on study for up to 8 weeks.
Who can join: Review the eligibility criteria below.
Location: University of California โ Riverside, California
Age range: 18 Years to 85 Years
๐งช Interventions in This Study
- C1 - Standard Perceptual Learning (SPL) (BEHAVIORAL)
- C2 - Long Training (LT) (BEHAVIORAL)
- C3 - Short Staircases (SS) (BEHAVIORAL)
- C4 - Mixed Difficulty (MD) (BEHAVIORAL)
- C5 - Noise Training (NT) (BEHAVIORAL)
- C6 - Training with Flankers (TWF) (BEHAVIORAL)
- C7 - Parafoveal Training (PT) (BEHAVIORAL)
- C8 - Stimulus Variety (SV) (BEHAVIORAL)
- C8a - Complex Features (CF) (BEHAVIORAL)
- C9 - Exogenous Attention Training (ExAT) (BEHAVIORAL)
- C10 - Endogenous Attention Training (EnAT) (BEHAVIORAL)
- C11 - Multisensory Facilitation (MF) (BEHAVIORAL)
- No Contact Control (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (3 Sites)
- University of California โ Riverside, California
- Northeastern University โ Boston, Massachusetts
- University of Wisconsin โ Madison, Wisconsin
๐ Contact the Study Coordinator
Phone: (626) 482-8091
Email: audreyc@ucr.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Cognitive Change
- Osteopathic Manipulation Makes a Neuropsychological Difference โ Downers Grove, Illinois
- Effectiveness of Cognitive Training in Older and Younger Adults โ Riverside, California
- Optimized Tailored Interventions in Metabolic and Lifestyle Outcomes (OPTIMAL) โ Urbana, Illinois
- Executive Function Training for Children and Adolescents โ Boston, Massachusetts
- Trout Consumption in Young Children and Families and Brain Health โ Moscow, Idaho
Explore by condition: All Cognitive Change clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.