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Computerized Cognitive Tests for Neurological Disease
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Recruiting
Led By Alexander Chervinsky, PhD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Participants will be male or female and between the ages of 21 and 65 years old.
Be older than 18 years old
Must not have
Participants without adequate perceptual and motor capacities preventing them from participation in the testing.
Participants with severe dysfunction at the level of dementia that can interfere with informed consent.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing three new computer-based tasks to measure brain and thinking skills. It involves both healthy people and those with neurological problems. The study aims to see if these new tasks are as good as traditional paper tests by comparing results from both methods.
Who is the study for?
This trial is for men and women aged 21-65, both healthy individuals and those with significant brain findings on neuroimaging. Participants must have good perception and motor skills to do the tests but can't join if they have severe dementia or lack the necessary perceptual/motor abilities.
What is being tested?
The study is testing three new computer-based cognitive function tests against traditional paper-and-pencil methods. It aims to see if these digital tasks are more effective by comparing results from healthy controls and patients with neurological impairments.
What are the potential side effects?
Since this trial involves non-invasive neuropsychological testing, there are no direct physical side effects expected from participating in this study.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 21 and 65 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am physically and mentally able to participate in tests.
Select...
I do not have severe dementia that affects my understanding.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
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: Non-CNI participantsActive Control10 Interventions
Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Group II: Cerebral neurological illness (CNI) participantsActive Control10 Interventions
Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for neurological diseases include pharmacological and non-pharmacological interventions. Pharmacological treatments, such as cholinesterase inhibitors and memantine, work by modulating neurotransmitter levels to improve cognitive and motor functions.
Non-pharmacological interventions, like computerized cognitive tests, aim to enhance brain function through structured cognitive exercises. These treatments are essential for neurological disease patients as they can slow disease progression, improve quality of life, and help maintain cognitive and motor functions.
Methodological recommendations for cognition trials in bipolar disorder by the International Society for Bipolar Disorders Targeting Cognition Task Force.
Methodological recommendations for cognition trials in bipolar disorder by the International Society for Bipolar Disorders Targeting Cognition Task Force.
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Who is running the clinical trial?
NYU Langone HealthLead Sponsor
1,409 Previous Clinical Trials
855,388 Total Patients Enrolled
Alexander Chervinsky, PhDPrincipal InvestigatorNYU Langone Health
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am physically and mentally able to participate in tests.I am between 21 and 65 years old.I do not have severe dementia that affects my understanding.I am between 21 and 65 years old.I can see, hear, and move well enough to take part in tests.
Research Study Groups:
This trial has the following groups:- Group 1: Non-CNI participants
- Group 2: Cerebral neurological illness (CNI) participants
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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