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LearningRx Cognitive Training for TBI

Not Applicable
Conditions
Traumatic Brain Injury (TBI)
Registration Number
NCT02918994
Lead Sponsor
Gibson Institute of Cognitive Research
Brief Summary

The purpose of this investigation is to conduct a series of case studies on the impact of LearningRx cognitive training on cognitive skills, brain structure, and daily functioning for participants with Traumatic Brain Injury (TBI).

Detailed Description

Using a multiple baseline design across cases with start point randomization, the proposed study will examine the outcomes from LearningRx one-on-one cognitive training across domains on standardized measures used to monitor treatment effectiveness for TBI.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
8
Inclusion Criteria
  • Age 18+ previously diagnosed with TBI
  • Living in the greater Colorado Springs area
Exclusion Criteria
  • No braces, metal implants, or claustrophobia that would contraindicate magnetic resonance imaging

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Evidence of overall cognitive function improvementwithin 14 days after completing the intervention

Confirmed by change in pretest to post-test scores on the Woodcock Johnson IV - Tests of Cognitive Abilities

Secondary Outcome Measures
NameTimeMethod
Evidence of reduction in TBI symptomswithin 14 days after completing the intervention

As confirmed by pretest to post-test changes on the Traumatic Brain Injury Checklist

Evidence of change in brain structurewithin 30 days after completing the intervention

Confirmed by change in pretest to post-test neuroimaging using MRI

Evidence of change in brain activitywithin 30 days after completing the intervention

As confirmed by pretest to post-test changes in electrical activity measured by qEEG

Evidence of improvement in visual attentionwith 14 days after completing the intervention

Confirmed by change in pretest to post-test scores on the Conners Continous Performance Test (CPT-3)

Evidence of improvement in auditory attentionwith 14 days after completing the intervention

Confirmed by change in pretest to post-test scores on the Auditory Attention Test (CATA)

Trial Locations

Locations (1)

Gibson Institute of Cognitive Research

🇺🇸

Colorado Springs, Colorado, United States

Gibson Institute of Cognitive Research
🇺🇸Colorado Springs, Colorado, United States

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