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Trial · NCT00547118

Registered outcomes14

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBrief Psychiatric Rating Scale (BPRS) Total ScoreBaseline (Week 0) and end of study (Week 16)
The total BPRS score is calculated by adding the scores for scales #1-#18. Each scale ranges from "1=Not Present" to "7=Very Severe". Total scores range from a minimum score of 18 to a maximum score of 126. A higher total score indicates a more severe psychiatric symptom rating.
PrimaryBrief Psychiatric Rating Scale (BPRS) Psychosis ScoreBaseline (Week 0) and end of study (Week 16)
The psychosis score is calculated by adding the scores for scales #4 Conceptual Disorganization, #11 Suspiciousness, #12 Hallucinatory Behavior, and #15 Unusual Thought Content. Each scale ranges from "1=Not Present" to "7=Very Severe". The minimum psychosis score is 4 and the maximum psychosis score is 28. A higher score indicates a more severe psychosis rating.
PrimaryThe Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)Baseline (Week 0) and end of study (Week 16)
The RBANS is a brief, individually administered test designed to evaluate neuropsychological status of adults, ages 20-89. The 12 subtests measure attention, language, visuospatial/constructional abilities, and immediate and delayed memory. The raw scores from the subtests are scaled together to create index scores, and these are summed for conversion to a total scale score. Higher score equals a better outcome. The total index score range for the RBANS is 40-160.
PrimaryThe Iowa Gambling Task (IGT)Baseline (Week 0) and end of study (Week 16)
The Iowa Gambling Task (IGT) is a computer-administered cognitive test that assesses risk preferences by simulating real-life decision making using uncertainty, rewards, and penalties. In the task, players are given four decks of cards and an endowment of fake money (e.g., $2000). Players are instructed to select cards one at a time and try to lose the least amount of money and win the most. The outcome measure was the number of rewarded minus punished card choices. Task has a maximum of 100 trials. The net score is the difference between the number of choices from advantageous decks verses disadvantageous decks. Higher scores are better and can range from -50 to +50.
PrimaryN-Back Neurocognitive Task: 0-back ConditionBaseline (Week 0) and end of study (Week 16)
The N-Back task is a sequential letter working memory task. D-prime was used to measure accuracy on the 0-back, 1-back, and 2-back conditions. D-prime scores range from 0 to 8.6. Higher scores are better. As memory load increases from 0 to 1, from 1 to 2, D-prime scores are expected to be lower.
PrimaryN-Back Neurocognitive Task: 1-back ConditionBaseline (Week 0) and end of study (Week 16)
The N-Back task is a sequential letter working memory task. D-prime was used to measure accuracy on the 0-back, 1-back, and 2-back conditions. D-prime scores range from 0 to 8.6. Higher scores are better. As memory load increases from 0 to 1, from 1 to 2, D-prime scores are expected to be lower.
PrimaryN-Back Neurocognitive Task: 2-back ConditionBaseline (Week 0) and end of study (Week 16)
The N-Back task is a sequential letter working memory task. D-prime was used to measure accuracy on the 0-back, 1-back, and 2-back conditions. D-prime scores range from 0 to 8.6. Higher scores are better. As memory load increases from 0 to 1, from 1 to 2, D-prime scores are expected to be lower.
SecondarySchedule for Assessment of Negative Symptoms (SANS) Total ScoreBaseline (Week 0) and end of study (Week 16)SANS total score range = 0-85. Higher scores indicate more severe negative symptoms.
SecondarySchedule for Assessment of Negative Symptoms (SANS) - AnhedoniaBaseline (Week 0) and end of study (Week 16)SANS Global Anhedonia score. Scores can range from 0-5, with higher scores indicating more severe anhedonia.
SecondarySchedule for Assessment of Negative Symptoms (SANS) - Blunted AffectBaseline (Week 0) and end of study (Week 16)SANS Global Rating of Affective Flattening. Scores can range from 0-5, with higher scores indicating more severe blunted affect.
SecondarySchedule for Assessment of Negative Symptoms (SANS) - AlogiaBaseline (Week 0) and end of study (Week 16)SANS Global Rating of Alogia. Scores can range from 0-5, with higher scores indicating more severe alogia.
SecondarySchedule for Assessment of Negative Symptoms (SANS) - AvolitionBaseline (Week 0) and end of study (Week 16)SANS Avolition score. Scores can range from 0-5, with higher scores indicating more severe avolition.
SecondaryClinical Global Impression (CGI)Baseline (Week 0) and end of study (Week 16)The global improvement score can range from 1-7, with higher scores indicating worse total improvement clinically.
SecondaryCalgary Depression Scale (CDS) Total ScoreBaseline (Week 0) and end of study (Week 16)
The CDS total score is the addition of scores from items 1-9. Each item's scores range on a scale of "0=Absent" to "3=Severe". The total score range is from 0-27. Higher total scores indicate a more severe depression rating.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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