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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02367898
Other study ID # LLI-001
Secondary ID
Status Completed
Phase N/A
First received February 13, 2015
Last updated September 9, 2015
Start date April 2013
Est. completion date April 2014

Study information

Verified date September 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 measure the efficacy of an online cognitive training program against an active control condition in a large, randomized trial.


Description:

The present study aims to evaluate a targeted, progressively challenging, online cognitive training program comprised of 49 distinct exercises targeting a variety of cognitive capacities. The cognitive training program will be compared to a plausibly beneficial active control condition in which participants completed online crossword puzzles.

The investigators hypothesize that the cognitive training will show greater transfer to a range of underlying cognitive abilities than the active control, as measured by a broad battery of neuropsychological assessments and participant-reported outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 11470
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Engaged with the Lumosity program at least 3 days in the first week after sign-up

- Access to an internet enabled computer to complete training

Exclusion Criteria:

- Paying subscriber

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


Intervention

Other:
Lumosity Cognitive Training
adaptive online cognitive training
Crossword Puzzles
timed online crossword puzzles

Locations

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

Sponsors (3)

Lead Sponsor Collaborator
Lumos Labs, Inc. Wayne State University, Wheaton College

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Aggregate Cognitive Performance Aggregate cognitive performance, as measured by Grand Index, on seven neuropsychological assessments (Forward Memory Span, Reverse Memory Span, Grammatical Reasoning, Progressive Matrices, Go/No-Go, Arithmetic Reasoning, Two-Target Search) Baseline to 10 weeks No
Secondary Participant-Reported Outcomes 9 questions related to everyday cognition and emotional status. Baseline to 10 weeks No
Secondary Individual Neuropsychological Assessments composite Separate analyses of changes on each of the seven neuropsychological assessments in the battery (Forward Memory Span, Reverse Memory Span, Grammatical Reasoning, Progressive Matrices, Go/No-Go, Arithmetic Reasoning, Two-Target Search). Baseline to 10 weeks No
See also
  Status Clinical Trial Phase
Completed NCT06199661 - High-Intensity Exercise in Older Adults N/A