Changes in Auditory Verbal Hallucination During Atypical Antipsychotic Treatment of Patients With Schizophrenia

Naturalistic Multicenter Study of Changes in Auditory Verbal Hallucination During Atypical Antipsychotic Treatment of Schizophrenia

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00328952

Enrollment

Registered

2006-05-24

Start date

2004-08-31

Completion date

2008-08-31

Last updated

2009-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hallucinations, Schizophrenia

Keywords

schizophrenia, auditory verbal hallucination, antipsychotic treatment

Brief summary

The purpose of this study is to evaluate the changes in various aspects of auditory verbal hallucinations during 24-week antipsychotic treatment in naturalistic condition.

Detailed description

Auditory verbal hallucinations (AVH), meaning the experience of hearing voices, occur in 60-75% of patients with schizophrenia. Patients experiencing persistent AVH tend to be interrupted in their daily routines and have trouble keeping regular jobs due to the intrusiveness or abusive contents of voices. In addition, auditory hallucinations are reported to remain even after disappearance of other psychotic symptoms in many patients with schizophrenia spectrum disorders after treatment with typical antipsychotics. The study involves detailed phenomenological assessments of AVH and other psychotic symptoms, as well as side effects of atypical antipsychotics.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

15 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

* Male or female patients, 15-65 years of age * Patients must have a diagnosis of schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV)\> * Patients experiencing vivid AVH confirmed by score of 4 or above using hallucinatory behavior item on Positive And Negative Syndrome Scale (PANSS). * Patients who are drug-naive or drug-free for more than 4 weeks. * Patients who are scheduled to receive atypical antipsychotic medication. * Each patient must provide written informed consent after full explanation of study protocol, and authorized legal guardian must understand the nature of the study and must also give assent to study participation. * Subjects who are fluent in Korean.

Exclusion criteria

* DSM-IV substance (except nicotine or caffeine) dependence within the past 1 year. * Mental retardation (IQ \< 70). * Neurological disorders including epilepsy, stroke, or severe head trauma. * Clinically significant laboratory abnormalities, on any of the following tests: CBC with differential, electrolytes, BUN, creatinine, hepatic transaminases, urinalysis and EKG. * Treatment with an injectable depot neuroleptic within less than three dosing interval between the last depot neuroleptic injections and baseline. * History of electroconvulsive therapy or transcranial magnetic stimulation within the past 3 months. * Subjects who are not fluent in Korean.

Countries

South Korea

Outcome results