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Behavioral Intervention

Cognitive Training for Cognitive Impairment

N/A
Waitlist Available
Led By Susanne M. Jaeggi, PhD
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
History of seizures, focal brain lesion, or head injury with loss of consciousness in the past year
Plans to travel out of the area for more than 1 week during the intervention period
Timeline
Screening 3 weeks
Treatment Varies
Follow Up end of post-test (up to 60 days)
Awards & highlights
No Placebo-Only Group

Summary

This trial will involve 1600 people to test if cognitive training works. Participants will be split into different groups and will take part in the study for up to 15 hours over 4 to

Who is the study for?
This trial is for individuals experiencing cognitive impairment. It's designed to include a wide age range, so both older and younger adults can participate. The main requirement is the ability to perform visual and/or auditory tasks.
What is being tested?
The study tests how effective different types of cognitive training are on improving mental functions. Participants will be randomly assigned to groups that receive either one or two types of visual/auditory tasks over a period of 4-8 weeks.
What are the potential side effects?
Since this trial involves non-invasive cognitive tasks, there are minimal expected side effects. Participants may experience fatigue or mental strain from the exercises.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had seizures, a brain injury, or was unconscious due to a head injury in the last year.
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I plan to travel for more than a week during the study.
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I have a physical disability that makes it hard for me to participate in training.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-test (baseline), post-test1 up to 30 days, (unmasked) post-test2 up to 60 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-test (baseline), post-test1 up to 30 days, (unmasked) post-test2 up to 60 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in the difference between the proportion of hits minus false alarms for a given level of the N-back task
Change in the difference of response time and accuracy in switch trials minus non-switch trials in the Task Switching Task
Change in the difference of response time in (i) switch trials minus non-switch trials and (ii) congruent minus incongruent trials in the Flanker Task
+11 more
Secondary study objectives
Behavioral Inhibition/Activation System (BIS/BAS) Score
Big-5-Inventory 10-item version (BFI-10) Score
Brief Pittsburgh Sleep Quality Index (B-PSQI) Score
+10 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Active Control
Group I: Long Testing GroupActive Control2 Interventions
Participants will go through 2 assessment sessions over 2-3 days (75 minutes each), followed by 10 sessions of cognitive tasks over 2 weeks in-lab or at-home, 1 session of 75 minutes about 2 weeks later, another 10 sessions of cognitive tasks over 2 weeks in-lab or at-home, then 2 sessions (\~45 minutes) over 2-3 days about 2 weeks after this session, and finally another 2 sessions (\~45 minutes) 3 days to 2 weeks after that session. Unless otherwise specified, all the sessions will take place in the lab.
Group II: Short Testing GroupActive Control1 Intervention
Participants will go through 2 assessment sessions over 2-3 days (\~75 minutes each), followed by 1 session of 75 minutes about 2 weeks later, 2 further sessions (\~45 minutes) over 2-3 days about 2 weeks after this session, and finally another 2 sessions (\~45 minutes) 3 days to 2 weeks after that session. All the sessions will take place in the lab.

Find a Location

Who is running the clinical trial?

University of Wisconsin, MadisonLead Sponsor
1,226 Previous Clinical Trials
3,167,074 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,782 Previous Clinical Trials
28,182,493 Total Patients Enrolled
Susanne M. Jaeggi, PhDPrincipal InvestigatorNortheastern University
~1067 spots leftby Jan 2028