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Brain Response to an Intervention Using Guided, At-Home Technology for the Mind

Brain Response to an Intervention Using Guided, At-Home Technology for the Mind - A Randomized, Controlled, Double-blinded, Parallel-group Intervention Study to Assess an At-Home Program for Improving Cognition and Inducing Changes in Brain Structure and Function

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05912556
Acronym
BRIGHT-Mind
Enrollment
817
Registered
2023-06-22
Start date
2023-07-17
Completion date
2025-03-11
Last updated
2026-09-15

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

Conditions

Brain Function, Brain Health, Brain Structure, Cognition

Brief summary

The objective of this study is to assess the effectiveness of two digital programs for providing mental stimulation, improving cognition, and inducing changes in brain structure and function.

Interventions

DEVICEDigital Program 1

2/3 of randomized subjects use digital program 1 for 12 weeks to provide mental stimulation

DEVICEDigital Program 2

1/3 of randomized subjects use digital program 2 for 12 weeks to provide mental stimulation

Sponsors

Lumos Labs, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects 25-80 years of age. * Ability to understand and speak English, follow written and verbal instructions (English), and give informed consent (English), as assessed by study staff. * Ability to comply with all the testing and study requirements, including the ability to independently use a video conferencing tool and the ability to independently use a computer to access the web. * Ability to independently complete a daily, online intervention and outcome assessments using a web browser compatible with the intervention and assessment software on a reliable, internet-connected laptop or desktop computer.

Exclusion criteria

* Current, controlled (requiring treatment) or uncontrolled psychiatric diagnosis, including but not limited to posttraumatic stress disorder, psychosis, bipolar illness, pervasive developmental disorder, severe obsessive compulsive disorder, severe depressive or severe anxiety disorder, conduct disorder, attention-deficit/hyperactivity disorder, or other symptomatic manifestations that in the opinion of the Investigator may confound study data/assessments. * Current, controlled (requiring treatment) or uncontrolled neurological diagnosis, including but not limited to Alzheimer's Disease, other dementias, mild cognitive impairment, Huntington's Disease, Parkinson's Disease, multiple sclerosis, stroke, epilepsy, aphasia, or other condition that in the opinion of the Investigator may confound study data/assessments. * Any other medical condition in the last 90 days that in the opinion of the Investigator may confound study data/assessments. * Has been under the care of a caretaker or has not been living independently in the last 90 days. * In the last three years has used any of the following for more than two weeks continuously: Online courses, Online brain training programs * Known sensitivity (such as headaches, dizziness, nausea) to bright, stimulating video displays. * History of seizures (excluding febrile seizures), or significant motor or vocal tics, including but not limited to Tourette's Disorder and photo-sensitive epilepsy. * Visual acuity that cannot be corrected that prevents or negatively impacts computer activity. * Has participated in a clinical trial within 90 days prior to screening. * Pregnancy or planning to become pregnant. Additional

Design outcomes

Primary

MeasureTime frameDescription
Overall Composite from Creyos (formerly Cambridge Brain Sciences)Study Day 0 to Study Day 84The Overall Composite is derived from the 12 tests in the Creyos battery.

Secondary

MeasureTime frameDescription
Concentration Domain Score from CreyosStudy Day 0 to Study Day 84
Memory Domain Score from CreyosStudy Day 0 to Study Day 84
Planning Domain Score from CreyosStudy Day 0 to Study Day 84
Reasoning Domain Score from CreyosStudy Day 0 to Study Day 84
Structural Brain Composite from Magnetic Resonance Imaging (MRI)Study Day 0 to Study Day 84Brain-predicted age difference (Brain-PAD)
White Matter Microstructure Composite from Diffusion Magnetic Resonance Imaging (dMRI)Study Day 0 to Study Day 84
Within-Network Functional Connectivity from Resting-State functional Magnetic Resonance Imaging (fMRI)Study Day 0 to Study Day 84

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKevin Madore, PhD

Lumos Labs, Inc.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026