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Clinical Trials/NCT02927197
NCT02927197
Completed
Not Applicable

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

Gibson Institute of Cognitive Research1 site in 1 country39 target enrollmentJune 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Learning Problems
Sponsor
Gibson Institute of Cognitive Research
Enrollment
39
Locations
1
Primary Endpoint
Evidence of overall cognitive function improvement
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
June 2015
End Date
June 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evidence of overall cognitive function improvement

Time Frame: within 14 days after completing the intervention

Confirmed by pretest to post-test change on the Woodcock Johnson III - Tests of Cognitive Abilities (WJ III): General Intellectual Ability composite score

Secondary Outcomes

  • Evidence of improvement in long-term memory(within 14 days after completing the intervention)
  • Evidence of improvement in working memory(within 14 days after completing the intervention)
  • Evidence of improvement in processing speed(within 14 days after completing the intervention)
  • Evidence of improvement in auditory processing(within 14 days after completing the intervention)
  • Evidence of improvement in school performance(Within two years after completing the intervention)
  • Evidence of improvement in fluid reasoning(within 14 days after completing the intervention)
  • Evidence of improvement in visual processing(within 14 days after completing the intervention)
  • Evidence of improvement in attention(within 14 days after completing the intervention)

Study Sites (1)

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