Mode
Text Size
Log in / Sign up
N/A N=60 Randomized Single-blind Treatment

Neurophysiological Targets for Cognitive Training in Schizophrenia

Schizophrenia

Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcome: Primary: Visual Target Detection (P300 Event-related Potential Amplitude) Change — 2.20; -0.72 microvolts (uV) — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Auditory Cognitive Training (Behavioral); Visual Cognitive Training (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Oct 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Visual Target Detection (P300 Event-related Potential Amplitude) Change
2.20; -0.72 <0.05 sig
PRIMARY
Auditory Mismatch Negativity (MMN) Amplitude Change
0.67; 0.51 <0.05 sig
PRIMARY
MCCB Cognitive Composite Score Change
-2.03; -2.45 <0.01 sig
SECONDARY
Visual Learning (BVMT-R) Change
-2.92; -3.24 0.06
SECONDARY
Verbal Learning (HVLT-R) Change
0.62; 0.03 0.55
SECONDARY
Visual Working Memory (Spatial Span) Change
-0.60; -0.92 0.63
SECONDARY
Auditory Working Memory (LNS) Change
-1.10; -1.47 0.26

Summary

The purpose of this study is to determine whether computer-based training of auditory and visual processing results in corresponding improvement in brain function in individuals with schizophrenia.

Eligibility Criteria

Inclusion Criteria

  • DSM-IV diagnosis of schizophrenia or schizoaffective disorder
  • Age between 18 & 70
  • minimum of 30 days since discharge from last hospitalization
  • minimum of 30 days since last change in psychiatric medications
  • receiving mental health services
  • no housing changes in the past 30 days

Exclusion Criteria

  • current diagnosis of alcohol or substance abuse
  • history of brain trauma or neurological disease
  • chart diagnosis of mental retardation or premorbid intelligence < 70 based on Wechsler Test of Adult Reading (WTAR) full-scale estimated IQ
  • auditory or visual impairment that would interfere with study procedures
  • a sample of 20 healthy community volunteers was also recruited according to these criteria and tested, without intervention, as a normative reference sample for MMN and P300 measures
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00923078). 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.

Back to search