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Clinical Trials/NCT00204087
NCT00204087
Unknown
Phase 3

Psychological Intervention for Persons at Risk of Psychosis in the Early Initial Prodromal State

University of Cologne1 site in 1 country126 target enrollmentJanuary 2001

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
University of Cologne
Enrollment
126
Locations
1
Primary Endpoint
transition to subthreshold psychosis (and psychosis or schizophrenia)
Last Updated
20 years ago

Overview

Brief Summary

The purpose of this randomized controlled trial is to develop a cognitive behavioral therapy (CBT) for persons with at risk mental states in the early initial prodromal state and to evaluate CBT in comparison to supportive counselling (SC).It is hypothesized that CBT is more effective than SC on transition to subthreshold psychosis, psychosis and schizophrenia as well as on prodromal symptoms and social adjustment.

Detailed Description

Several studies indicated that self-perceived cognitive thought and perception deficits (basic symptoms), negative symptoms, anxiety, depressive symptoms and social stagnation or social decline are usually present years before the first episode of schizophrenia appears. It is also known that delayed treatment of schizophrenia correlates with a poor prognosis, low compliance and high family burden. As consequence of these findings, for the first time we developed a cognitive behavioral therapy (CBT) for persons at risk for psychosis in the early initial prodromal state. The early initial prodromal state was defined by the presence of self-perseived neuropsychological deficits, which were found to be predictive for transition to psychosis and by the presence of clinical relevant decline of functioning in combination with that of clinical management (CM). Is CBT more effective than CM with regard to the three aims of intervention 1. transition to psychosis, 2. improvement of prodromal symptoms, 3. prevention of social decline/stagnation, ? A randomized controlled trail is used to compare the efficacy of CBT with that of supportive counselling (SC). Patients are randomized to receive either CBT or SC over a 12 months period. CBT comprises of individual and group therapy as well as cognitive remediation and psychoeducation for key persons. SC should provide regular supportive contacts for the patient. No CBT strategies are allowed to be systematically applied in SC.

Registry
clinicaltrials.gov
Start Date
January 2001
End Date
June 2005
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • General criteria
  • Age between 17 and 36 years
  • male or female, in- or outpatients
  • written informed consent, for patients below 18 years also signed by their parents
  • Special criteria (presented within the last three months prior to the study)
  • Self-experienced neuropsychological deficits (basic symptoms)
  • Thought interferences
  • Compulsory like perseverance of thoughts
  • Thought pressure
  • Thought blockages

Exclusion Criteria

  • Attenuated or transient positive symptomes
  • Present or past diagnosis of a schizophrenic, schizophreniform, schizoaffective, delusional or bipolar according to DSM IV
  • Present or past diagnosis a brief psychotic disorder according to DSM IV with a duration of more than one week or within the last 4 weeks regardless of its duration
  • Diagnosis of delirium, dementia, amnestic or other cognitive disorder, mental retardation psychiatric disorder due to a somatic factor or related to the consumption of psychotropic substances according DSM IV
  • Alcohol- or drug abuse within the last three months prior to inclusion according to DSM IV
  • Deases of the central nervous system (inflammatory, traumatic, epilepsy etc.)

Outcomes

Primary Outcomes

transition to subthreshold psychosis (and psychosis or schizophrenia)

Secondary Outcomes

  • improvement of prodromal symptoms (basic symptoms, depression, anxiety)
  • social adjustment

Study Sites (1)

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