PC-Based Cognitive Rehabilitation for Traumatic Brain Injury (TBI)

NCT00927576 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 265

Last updated 2015-07-31

Study results available
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Summary

The investigators evaluated whether it was possible to improve the measurement of memory, attention, and executive function in patients who have suffered traumatic brain injury through the use of computer-based testing.

Note: the original design of the study was altered due to failure to recruit sufficient numbers of patients who were willing to undergo prolonged cognitive training.

Conditions

Interventions

BEHAVIORAL

Digit span testing

Testing of short-term verbal memory with digit span

BEHAVIORAL

Spatial span testing

Testing of short-term visuospatial memory with spatial span.

BEHAVIORAL

Finger tapping

Testing motor speed with a finger tapping test.

BEHAVIORAL

Simple reaction time

Testing the time to respond to the appearance of a visual stimulus.

BEHAVIORAL

Choice reaction time

Testing the time needed to discriminate and respond to different visual stimuli.

BEHAVIORAL

Verbal fluency

Evaluating how many words are produced in 90s.

BEHAVIORAL

Verbal list learning

Evaluating short-term memory, learning, and memory interference in the recall of 12-word lists, presented three times. Evaluating long-term memory and recognition after a 20 min interval.

BEHAVIORAL

Trail making test

Evaluating visuomotor speed and executive function in Trail Making Tests, A and B. In the first, subjects connect successive numbers with the mouse. In the second, they connect numbers and letters in alternation.

BEHAVIORAL

Design fluency

Subjects create the maximal number of 4-line patterns in 90 s.

BEHAVIORAL

Questionnaire completion

Question completion time is measured on each question of the Post-Traumatic Stress Disorder check list (PCL) and on the cognitive failures questionnaire.

Sponsors & Collaborators

Principal Investigators

  • David L. Woods, PhD · VA Northern California HCS

Eligibility

Min Age
18 Years
Max Age
78 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2013-03-31
Completion
2013-03-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00927576 on ClinicalTrials.gov