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Study identifier: NCT07171450 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Cognitive Remediation

Condition: Aging · Inflammation · Cognitive Remediation  ·  Sponsor: Cutter Lindbergh

PhaseNA
Planned participants75
Who can joinAll sexes, 60 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to determine if a neuroscience-based computerized cognitive remediation ("brain training") program can treat neurocognitive dysfunction (i.e., memory or thinking difficulties) that emerges in some older adults following a viral infection. The main questions it aims to answer are: * Does computerized cognitive remediation improve cognitive performance and day-to-day functioning in older adults with postviral neurocognitive dysfunction? * Will treatment effects be maintained over time, leading to better long term cognitive outcomes? * Does the treatment lead to reductions in blood-based markers of inflammation as a potential mechanism of cognitive symptom improvement? * Can the treatment be optimized and refined based on feedback from participants to improve user (patient) experience? Researchers will compare the computerized cognitive remediation program to an active computer-based control condition (alternative computer activities) to see if the computerized cognitive remediation program works to treat postviral neurocognitive dysfunction. Participation takes approximately 43-48 hours over 7 months, with most activities (40-46 hours) completed within the first 7-8 weeks, including: * Initial intake visit: Eligibility confirmation (\~2-3 hours) * Computer activities: About 5 hours per week for \~6 weeks (total \~30 hours) completed on a computer tablet provided by the study and loaned to participants for use during the treatment phase * We…

This description comes directly from the study's public registry record.

Talk to the study team

Holly Eddy, Ph.D., LMFT-S  ·  860-679-3751  ·  eddy@uchc.edu

Jennifer Brindisi, M.A.  ·  860-679-7581  ·  brindisi@uchc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UConn HealthFarmington, Connecticut, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07171450