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Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults

Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02518204
Enrollment
229
Registered
2015-08-07
Start date
2015-07-31
Completion date
2017-02-28
Last updated
2017-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Keywords

cognitive assessment, neuropsychological assessment, Brain Performance Test, computerized assessment

Brief summary

The purpose of this study is to evaluate the concurrent validity between the Brain Performance Test (BPT) subtests and corresponding conventional in-person neuropsychological assessments (NP).

Detailed description

This will be a multi-site, randomized, counterbalanced, two-period, two-sequence, validation study of the online, unsupervised Brain Performance Test (BPT). Over the course of 14 days, participants will complete two in-clinic visits during which they will complete both the BPT and in-person neuropsychological assessments (NP).

Interventions

OTHERBPT

Brain Performance Test (BPT) computerized cognitive assessment battery developed by Lumos Labs, Inc.

OTHERNP

Conventional in-person Neuropsychological Assessments (NP) Subtests from: * HRB: Halstead-Reitan Battery * MATRICS: Measurement and Treatment Research to Improve Cognition in Schizophrenia * WAIS-IV: Weschler Adult Intelligence Scale - IV

Sponsors

Collaborative Neuroscience Network
CollaboratorUNKNOWN
Lumos Labs, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
70 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

* Native English speaker * Capable and willing to provide informed consent * Able to use a computer and mouse without assistance * Limited (\< 3 days) or no experience with Lumosity.com * Limited (\< 3 days) or no experience with other cognitive training programs (e.g., FitBrains, CogMed) * Willing to refrain from online cognitive training during the course of the study * No recent (\<1 years) experience with either computer-based or in-person neuropsychological tests (e.g., WAIS-IV, WISC, Halstead-Reitan Battery, MATRICS, CogState, CNS Vital Signs) * Good general health assessed via self-reported online physical questionnaire and medical history questionnaire

Exclusion criteria

* Illiterate or unable to understand written English sufficiently to comprehend study instructions and consent form * Uncorrected visual impairment (beyond that required to qualify for a California Driver's License) that may impact the ability to complete assessments (self-report or determined by the clinician) * Uncorrected auditory impairment that may impact the ability to complete assessments (self-report or determined by the clinician) * Self-reported clinical diagnosis for primary psychiatric or neurological disorder (e.g., schizophrenia, multiple sclerosis, attention deficit hyperactivity disorder, Parkinson's disease, epilepsy) * Self-reported history of concussion or traumatic brain injury, that is considered clinically significant in the opinion of the investigator (e.g. loss of consciousness ≤ 30 minutes) * Self-reported diagnosis of mental retardation or pervasive developmental disorder * Self-reported diagnosis of Mild Cognitive Impairment, Alzheimer's disease, or other dementia * Self-reported history of sustained substance or alcohol abuse or dependence, that is considered clinically significant in the opinion of the investigator (e.g. as defined by DSM-5) * Self-report that subject is currently taking an antipsychotic, antidepressant, anti-anxiety, or a cognitively-enhancing medication (e.g. Ritalin), or in the last 72 hours, narcotics for pain or other medications that may impact cognitive performance (e.g. sleeping medications/aides or cold/allergy medications) * Any other significant medical condition that could impact cognitive performance or result in cognitive impairment in the opinion of the investigator * Score \<28 on the MMSE * Positive urine test for recent substance use on either testing day * Breath Alcohol Content of 0.01% or greater on either testing day

Design outcomes

Primary

MeasureTime frame
Correlation coefficients (Pearson's r) of scaled scores of BPT subtests compared to scaled scores of their NP correlates at Time 11 day

Secondary

MeasureTime frame
Correlation coefficients (Pearson's r and ICC) of raw scores of BPT subtests compared to raw scores of their NP correlates at Time 11 day
Correlation coefficients (Pearson's r and ICC) of BPT composite indices and NP composite indices at Time 11 day
Interclass correlations (ICC) of scaled scores of BPT subtests compared to scaled scores of their NP correlates at Time 11 day
Correlation coefficients (Pearson's r and ICC) of composite indices of BPT and NP at Time 1 and Time 2 as measures of reliability2 weeks
Correlation coefficients (Pearson's r and ICC) of BPT Grand Index and NP Overall Index at Time 1 and Time 2 as measures of reliability2 weeks
Correlation coefficients (Pearson's r and ICC) of raw and scaled scores of BPT subtests at Time 1 and Time 2 as measures of test-retest reliability2 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026