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Cogmed for Working Memory After TBI

Not Applicable
Completed
Conditions
Traumatic Brain Injury
Interventions
Behavioral: Cogmed
Registration Number
NCT02305212
Lead Sponsor
Kessler Foundation
Brief Summary

This study will examine a cognitive rehabilitation protocol targeted at working memory deficits for adults and children with Traumatic Brain Injury (TBI). In this randomized clinical trial, the efficacy of Cogmed, a cognitive rehabilitation protocol designed to improve working memory, will be examined in children with TBI. Neuropsychological and daily life functioning will be measured. Participants will be children (N=20) and adults (N=20) with a documented history of TBI. Participants will be randomized to a treatment group or a wait list control group. The Experimental Group will receive the Cogmed working memory training program 30-40 minutes per day, 5 days a week for 5 weeks for a total training time of approximately 15 hours. The Control Group will be a wait list control group that will cross over into treatment after the follow-up assessment. All subjects will undergo repeat assessments following completion of the working memory training protocol after the 7th week and again at 13 weeks to document changes in working memory performance.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • History of Traumatic Brain Injury
Exclusion Criteria
  • Diagnosis of other neurological conditions

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
CogmedCogmedCogmed is a cognitive rehabilitation protocol designed to improve working memory. The Cogmed sessions are on a computer at home for 30-40 min per day, 5 days per week for 5 weeks.
Primary Outcome Measures
NameTimeMethod
Change in scores on standardized tests of working memoryThree points in time: Baseline assessment, Week 7 and Week 13

Measured via standardized neuropsychological tests (i.e. paper and pencil testing)

Secondary Outcome Measures
NameTimeMethod
Change in scores on self report measures of memory functioning, assessed via questionniareThree points in time: Baseline assessment, Week 7 and Week 13
Change in scores on self report measures of emotional functioning, assessed via questionnaireThree points in time: Baseline assessment, Week 7 and Week 13
Change in scores on self report measures of quality of life, assessed via questionnaireThree points in time: Baseline assessment, Week 7 and Week 13

Trial Locations

Locations (2)

Childrens Specialized Hosptial

🇺🇸

Mountainside, New Jersey, United States

Kessler Foundation

🇺🇸

West Orange, New Jersey, United States

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