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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02382393
Other study ID # LL002(p)
Secondary ID
Status Completed
Phase N/A
First received March 3, 2015
Last updated November 11, 2015
Start date March 2015
Est. completion date November 2015

Study information

Verified date November 2015
Source Lumos Labs, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the concurrent validity (correlation coefficient of scores at 1 time point) between the Brain Performance Test (BPT, Lumos Labs, Inc.) and a validated third party computerized assessment.


Description:

Each subject will complete two sessions, each approximately 1 hour in total duration, approximately 2 weeks apart for a total duration of participation of 2 hours over 2 weeks


Recruitment information / eligibility

Status Completed
Enrollment 1152
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Electronically signed informed consent

- 18 years of age or older

- Native English-Speaker

- Consistent access to a computer with stable internet connection

Exclusion Criteria:

- Under 18 years of age

- Native language other than English

- Visual impairment that impedes computer use

- Has taken a cognitive assessment or done cognitive training in the past year

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Other:
Brain Performance Test (BPT, Lumos Labs, Inc)
A brief, repeatable, online battery of cognitive assessments used to measure functioning in five cognitive domains across time.
Computerized Assessment
a validated, computerized cognitive assessment tool

Locations

Country Name City State
United States Lumos Labs, Inc. San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
Lumos Labs, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary BPT Grand Index Score at Time 1 Baseline No
Primary Computerized Assessment Index at Time 1 Baseline No
Primary Selected raw and scaled BPT and Computerized Assessment matched subtest scores at Time 1 Baseline No
Secondary BPT Grand Index at Time 1 and Time 2 Baseline to 2 weeks No
Secondary Computerized Assessment Index at Time 1 and Time 2 Baseline to 2 weeks No
Secondary Raw and scaled BPT subtest scores at Time 1 and Time 2 Baseline to 2 weeks No
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