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The efficacy of Cognitive- Remediation Therapy on symptoms and function improvement in Patients with Schizophrenia

The efficacy of Cognitive- Remediation Therapy on symptoms and function improvement in Patients with Schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138901282511N5
Enrollment
40
Registered
2010-04-17
Start date
2008-12-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Schizophrenia. Schizophrenia

Interventions

Intervention 1: Intervention group: Cognitive remediation therapy, 16 sessions which last 45 minutes, 2 session in a week. Each session had a defined structure. Therapsists were 5 exprienced and train
Rehabilitation
Intervention group: Cognitive remediation therapy, 16 sessions which last 45 minutes, 2 session in a week. Each session had a defined structure. Therapsists were 5 exprienced and trained psychologists
Control group: no intervention

Sponsors

University of Social Welfare and Rehabilitation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Having a certain diagnosis of schizophrenia according to both DSMIV- TR criteria and psychiatrist diagnosis and SCID structured interview confirm the diagnosis, age 25 to 50 years, havivg persistent symptoms for at least 1 year despite adequate trials of antipsychotic medication, education level of at least grade 5 Exclusion criteria: Having brain injury, dementia, or any specific neurological disorder which need special care, not being in acute phase, having evidences for serious side effects of any antipsychotic drugs which leads to specific treatment other than treatment as usual, current abuse or poisoning or withdrawal of drugs (using cigarette as usual is not criteria for exclusion), receiving ECT for at least 6 months prior to or during the therapy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Negative symptoms. Timepoint: before treatment- session8- after treatment. Method of measurement: Negative symptoms scale (SANS).;Positive symptoms. Timepoint: before treatment- session8- after treatment. Method of measurement: Positive symptoms scale (SAPS).;Behavioral function. Timepoint: Before treatment- session 8- After treatment. Method of measurement: Behavioral function scale (NOSIE).;Cognitive function. Timepoint: Before treatment- session 8- After treatment. Method of measurement: Cognistat (NCSE).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Ali beigi

University of Social Welfare and Rehabilitation

nedapsych@yahoo.com+98 21 8842 2868

Outcome results

None listed

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