Neurocognitive Effectiveness in Treatment of First-episode Non-affective Psychosis: 1-year Follow-up

PHASE4CompletedINTERVENTIONAL
Enrollment

136

Participants

Timeline

Start Date

October 31, 2005

Primary Completion Date

January 31, 2011

Study Completion Date

January 31, 2013

Conditions
SchizophreniaPsychotic Disorders
Interventions
DRUG

Aripiprazole

Oral, dose range 5-30 mg/day, once or twice a day, during study duration

DRUG

Quetiapine

Oral, dose range 100-600 mg/day, once or twice a day, during study duration

DRUG

Ziprasidone

Oral, dose range 40-160 mg/day, once or twice a day, during study duration

BEHAVIORAL

Cognitive battery

Completed in the following standardized sequence: 1-the Rey Auditory Verbal Learning Test (RAVLT); 2-WAIS-III digit symbol subtest; 3-Grooved Pegboard Test; 4-The Zoo Map Test; 5-Tower of London Test (ToL); 6-Rey Complex Figure (RCF); 7-Trail Making Test (TMT); 8-WAIS-III digits forward and backward subtests; 9-WAIS-III letter-number sequencing subtest; 10-WAIS-III vocabulary subtest that was used as measure of premorbid intelligence quotient (IQ); 11-Stroop Test; 12-letter (FAS) and semantic (animal) fluency tests; 14-Eyes Task; 15-Continuous Performance Test (CPT).

Trial Locations (1)

39008

University Hospital Marqués de Valdecilla, Santander

All Listed Sponsors
collaborator

Centro de Investigación Biomédica en Red de Salud Mental

NETWORK

collaborator

Instituto de Investigación Marqués de Valdecilla

OTHER

lead

Fundación Marques de Valdecilla

OTHER

NCT02534363 - Neurocognitive Effectiveness in Treatment of First-episode Non-affective Psychosis: 1-year Follow-up | Biotech Hunter | Biotech Hunter