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Cognitive Training

LearningRx cognitive training for Traumatic Brain Injury

N/A
Waitlist Available
Led By Christina Ledbetter, PhD
Research Sponsored by Gibson Institute of Cognitive Research
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up with 14 days after completing the intervention
Awards & highlights

Study Summary

This study is evaluating whether cognitive training can improve cognitive skills in people with traumatic brain injury.

Eligible Conditions
  • Traumatic Brain Injury

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~with 14 days after completing the intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and with 14 days after completing the intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Evidence of overall cognitive function improvement
Secondary outcome measures
Evidence of change in brain activity
Evidence of change in brain structure
Evidence of improvement in auditory attention
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: LearningRx cognitive trainingExperimental Treatment1 Intervention
The intervention is a 60-hour, clinician-delivered cognitive training program.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
LearningRx cognitive training
2015
N/A
~50

Find a Location

Who is running the clinical trial?

Gibson Institute of Cognitive ResearchLead Sponsor
3 Previous Clinical Trials
47 Total Patients Enrolled
Amy L Moore, PhDStudy DirectorGibson Institute of Cognitive Research
2 Previous Clinical Trials
8 Total Patients Enrolled
Christina Ledbetter, PhDPrincipal InvestigatorGibson Institute of Cognitive Research
2 Previous Clinical Trials
8 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~1 spots leftby May 2025