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Behavioural Intervention

Brain-Training Exercises for Long COVID

N/A
Recruiting
Led By Cutter Lindbergh, Ph.D.
Research Sponsored by UConn Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age ≥ 55 years old
TICS ≥ 27
Must not have
Significant sensory or motor impairments (e.g., blindness) that may interfere with the ability to complete neuropsychological measures or engage in the intervention
History of neurological disorder or other medical condition with potential to impair cognitive functioning or interfere with study participation (e.g., epilepsy, stroke, dementia, head trauma followed by persistent neurological deficits or known structural brain abnormalities)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up our feasibility criteria will be assessed by calculating percentages at the conclusion of the study
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing if computerized brain-training exercises can help older adults with Long COVID. The goal is to see if these exercises can improve thinking, mood, and daily activities. The study will check if the exercises are easy to use and if they actually help.

Who is the study for?
This trial is for older adults (55+) who've had COVID-19 and are experiencing ongoing cognitive symptoms that started after their illness. They should be fluent in English, have a certain level of cognitive function (TICS ≥ 27), and not planning to change any psychiatric medication doses during the study. People with neurological disorders, prior cognitive impairments unrelated to COVID-19, significant psychiatric conditions, recent substance use disorders, or major sensory/motor issues can't participate.
What is being tested?
The trial is testing 'NeuroFlex', which involves computerized brain-training exercises designed as games. The goal is to see if these exercises can help improve thinking, mood, and daily functioning in older adults suffering from Long COVID's lingering effects on cognition.
What are the potential side effects?
Since this intervention involves non-invasive computer tasks, side effects are minimal but may include eye strain or mild frustration due to the nature of brain-training activities.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 55 years old or older.
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My thinking and memory test score is 27 or higher.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I do not have major sensory or motor issues that would stop me from participating in the study.
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I do not have any brain conditions that could affect my thinking or participation.
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I was diagnosed with Mild Cognitive Impairment not related to COVID-19.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the investigators will evaluate change in total fas score at post-treatment (6 weeks) relative to pre-treatment (baseline)
This trial's timeline: 3 weeks for screening, Varies for treatment, and the investigators will evaluate change in total fas score at post-treatment (6 weeks) relative to pre-treatment (baseline) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Credibility/Expectancy Questionnaire (CEQ)
Feasibility (proportion of subjects who agree to participate in the offered treatment, complete assigned exercises, and complete the entire treatment regimen)
System Usability Scale (SUS)
+1 more
Secondary study objectives
California Verbal Learning Test (CVLT)
Everyday Cognition (ECog)
Fatigue Assessment Scale (FAS)
+6 more

Awards & Highlights

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

Trial Design

1Treatment groups
Experimental Treatment
Group I: Computerized Cognitive RemediationExperimental Treatment1 Intervention

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
Computerized brain-training exercises aim to improve cognitive function through structured mental activities that target specific brain regions involved in memory, attention, and problem-solving. These exercises stimulate neuroplasticity, the brain's ability to reorganize itself by forming new neural connections. For Long COVID Syndrome patients, who often experience cognitive impairments such as brain fog, these exercises can potentially enhance cognitive recovery, improve mood, and support better overall daily functioning.

Find a Location

Who is running the clinical trial?

National Institute on Aging (NIA)NIH
1,785 Previous Clinical Trials
28,184,696 Total Patients Enrolled
UConn HealthLead Sponsor
213 Previous Clinical Trials
60,579 Total Patients Enrolled
Cutter Lindbergh, Ph.D.Principal InvestigatorUConn Health

Media Library

NeuroFlex (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05705193 — N/A
Long COVID Syndrome Research Study Groups: Computerized Cognitive Remediation
Long COVID Syndrome Clinical Trial 2023: NeuroFlex Highlights & Side Effects. Trial Name: NCT05705193 — N/A
NeuroFlex (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05705193 — N/A
Long COVID Syndrome Patient Testimony for trial: Trial Name: NCT05705193 — N/A
~2 spots leftby Dec 2024