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LearningRx Brain Training for Children 8-14

A Randomized, Controlled Study on the Effects of LearningRx Brain Training for Improving Cognitive Skills in Students Ages 8-14

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02927197
Enrollment
39
Registered
2016-10-06
Start date
2015-06-30
Completion date
2017-06-30
Last updated
2018-02-15

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

Conditions

Learning Problems

Brief summary

The purpose of this study is to examine changes in multiple cognitive skills after completing 60 hours of cognitive training with ThinkRx, a LearningRx program.

Detailed description

In a two-phase randomized controlled study, investigators will examine the effects of a one-on-one cognitive training program on memory, visual and auditory processing, processing speed, reasoning, attention, and General Intellectual Ability (GIA) score for students ages 8-14. In Phase 1, participants will be randomly assigned to either an experimental group to complete 60 hours of one-on-one cognitive training or to a wait-list control group. In Phase 2, the wait-list control group will complete the intervention using an alternative delivery model: 50% clinician delivered and 50% digital delivery.

Interventions

A clinician will deliver forty 90-minute cognitive training sessions over 12-14 weeks for a total of 60 training hours. There are 23 different categories of training procedures sequenced in intensity and difficulty for a total of more than 1000 training tasks.

Sponsors

Gibson Institute of Cognitive Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
8 Years to 14 Years
Healthy volunteers
Yes

Inclusion criteria

* Between 8-14 years of age, living in the greater Colorado Springs area, screening GIA score between 70 and 130

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Evidence of overall cognitive function improvementwithin 14 days after completing the interventionConfirmed by pretest to post-test change on the Woodcock Johnson III - Tests of Cognitive Abilities (WJ III): General Intellectual Ability composite score

Secondary

MeasureTime frameDescription
Evidence of improvement in working memorywithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Numbers Reversed test
Evidence of improvement in long-term memorywithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Visual-Auditory Learning Delayed test
Evidence of improvement in fluid reasoningwithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Concept Formation test
Evidence of improvement in school performanceWithin two years after completing the interventionConfirmed by improvement in school achievement tests and grade reports
Evidence of improvement in visual processingwithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Spatial Relations test
Evidence of improvement in auditory processingwithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Sound Blending test
Evidence of improvement in attentionwithin 14 days after completing the interventionConfirmed by pretest to posttest change on the National Institutes of Health (NIH) Cognition Toolbox attention test
Evidence of improvement in processing speedwithin 14 days after completing the interventionConfirmed by pretest to posttest change on the WJ III: Visual Matching test

Countries

United States

Outcome results

None listed

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