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Prospective Memory in Children with Traumatic Brain Injury - Article


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Brain Injury

 




Clinical Trial: Prospective Memory in Children with Traumatic Brain Injury

This study is currently recruiting patients.

Sponsored by: National Institute of Child Health and Human Development (NICHD)
Information provided by: National Institute of Child Health and Human Development (NICHD)

Purpose

Prospective memory (PM) is memory to complete future tasks, such as recalling to give a note to someone when you next see them, pick up milk on the way home, or remembering to keep an appointment. This study will evaluate PM in children with traumatic brain injury (TBI).

Condition
Traumatic Brain Injury

MedlinePlus related topics:  Head and Brain Injuries

Study Type: Observational
Study Design: Psychosocial, Cross-Sectional, Defined Population, Prospective Study

Official Title: Prospective Memory in Normal and Head-Injured Children

Further Study Details: 

Expected Total Enrollment:  178

Study start: July 2002;  Expected completion: June 2006

While much has been learned about how children with TBIs learn and recall stories, word lists, and pictures, little is known about how they perform PM tasks. Impairment in PM could have serious implications for academic and vocational pursuits. This study will investigate PM in children with mild or severe TBI. The study will focus on three major themes: 1) strategies that may help children with TBI overcome or minimize their PM deficits; 2) how specific areas of cognition can be impaired following TBI and in turn impair PM; and 3) the impact of PM deficits on a child’s daily functioning, both at school and at home. The study will also evaluate children without TBI (control group).

Each child will participate in one study evaluation. The evaluation will last approximately 4 hours, with a lunch break and other rest breaks as necessary. Assessments will include neuropsychological tests of attention, memory, and general intellectual functioning. Experimental tasks will include measures of metacognition for prospective memory, elucidation of strategic versus automatic processes involved in PM, and the effect of motivation manipulations in overcoming PM deficits with varying working memory loads. The child’s parent or guardian will also be asked to complete some tests to measure the impact of PM deficits on the child’s daily home life.

Eligibility

Ages Eligible for Study:  12 Years   -   18 Years,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria

  • English speaker
  • Minimum birth weight of 2500 grams (5.5 lbs) and 37 weeks’ gestation

Additional Inclusion Criteria for Children with Traumatic Brain Injury

  • Head injury resulting in a post-resuscitation Glasgow Coma Scale score of either 13 to 15 or 3 to 8
  • No evidence of hypoxic injury

Exclusion Criteria

  • History of epilepsy, mental retardation, or documented evidence of developmental dysfunction
  • Previous hospitalization for head injury involving loss of consciousness or postconcussional symptoms
  • History of autism, major psychiatric disorder, or pervasive developmental delay
  • History of meningitis or encephalitis
  • History of child abuse
  • History of chronic or uncontrolled serious physical disorders (cancer, uncontrolled diabetes, cystic fibrosis, etc.)
  • Note: siblings of participants with TBI or orthopedically-injured comparison children will not be enrolled to maintain the independence of the groups

Location and Contact Information


Texas
      Baylor College of Medicine, Houston,  Texas,  77030,  United States; Recruiting
Stephen R. McCauley, Ph.D.  713-798-7479    mccauley@bcm.tmc.edu 

Study chairs or principal investigators

Stephen R. McCauley, Ph.D.,  Principal Investigator,  Baylor College of Medicine   

More Information

Study ID Numbers:  K23HD40896
Record last reviewed:  May 2003
Last Updated:  October 13, 2004
Record first received:  May 27, 2003
ClinicalTrials.gov Identifier:  NCT00061399
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 3, 2009



Page Updated: October 3, 2005
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