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A study of the cognitive behavior therapy for first-episode schizophrenia

A study of the cognitive behavior therapy for first-episode schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003929
Enrollment
Unknown
Registered
2013-07-12
Start date
2012-06-02
Completion date
Unknown
Last updated
2018-05-14

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

Conditions

schizophrenia

Interventions

Cognitive and behavioral therapy group:antipsychotics combined with CBT
routine group:routine antipsychotics

Sponsors

Beijing anding hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Patients with a diagnosis of schizophrenia based on DSM-IV; 2. Age between 16 and 45 years; 3. The first time attack, or the length of illness less than 3 years and continuous treatment less than 1 month or intermittent treatment less than 3 months; 4. Using a single atypical antipsychotic drug treatment at present; 5. The total score of delusion(p1) or illusion(p3)>/=four points according to Positive And Negative Syndrome Scale (PANSS); 6. The informed consent of patients and their families.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. With other mental diseases; 2. Patients have attack or impulsive behavior, and need be constrained; 3. Modified electroconvulsive therapy; 4. Accepting other system psychological therapy or physical therapy; 5. Combine with serious or unstable physical diseases.

Design outcomes

Primary

MeasureTime frame
The positive and negative symptoms of schizophrenia;The Psychotic Symptom Rating Scales (PSYRATS);Effect rate, recurrent rate, rate of re-hospitalization;

Secondary

MeasureTime frame
SAI, PSP, on working status;

Countries

China

Contacts

Public ContactZhanjiang Li

Beijing Anding hospital affiliated to capital medical university

lizhanjiang1221@sina.com+86 010 58303004

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026