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N/A N=142

Memory and the Hippocampus in Twins

PTSD · Stress Disorders, Post-Traumatic

Enrolled (actual)
142
Serious AEs
0.0%
Results posted
Jan 2015
Primary outcome: Primary: Neuropsychological Testing of Memory — 77; 82 percentage of WMS retention

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 50+ yrs
Sex
Male
Sponsor
US Department of Veterans Affairs
Primary completion
Jun 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Neuropsychological Testing of Memory
77; 82

Summary

The purpose of this project is to measure brain markers and cognitive factors in twins with a history of military service with and without PTSD, and to follow them over time and measure changes in brain function and cognitive variables.

Eligibility Criteria

Inclusion Criteria

  • All twins will be required to give written informed consent.
  • Subjects will be included with a history of Vietnam Era service.
  • All subjects must be free of major medical illness on the basis of history and physical examination, lab testing, and electrocardiogram.

Exclusion Criteria

  • Subjects will be excluded with a history of shrapnel or other foreign bodies that would preclude MRI scanning, history of loss of consciousness, or neuroleptics, sedative or benzodiazepine medication usage within the previous four weeks.
  • Subjects will also be excluded if based on the SCID interview they have comorbid:
  • schizophrenia;
  • schizoaffective disorder;
  • bulimia or anorexia, or
  • bipolar disorder.
  • Subjects will also be excluded with a history of blast injury with associated traumatic brain injury.
  • In addition, subjects will be excluded with a history of alcohol or substance abuse/dependence within the past year. We will use the strategy used in prior MRI studies and use multivariate analyses to examine the contribution of past histories of alcohol and substance abuse (as measured with the Addiction Severity Index) and depression symptom level (as measured with the Hamilton Depression Scale) to the outcomes of interest.
  • Subjects will be excluded from the study if they present with a history of serious medical or neurological illness, or as a result of routine laboratory studies, history of asthma, steroid usage, seizure disorder, or prenatal/perinatal substance exposure or trauma.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00638885). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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