Depression Clinical Trial
Official title:
Comparison of the Effectiveness of the Virtual Environment in Cognitive Rehabilitation With Standard Rehabilitation Methods in Patients With Schizophrenia and in Patients With Major Depressive Disorder
Verified date | March 2021 |
Source | National Institute of Mental Health, Czech Republic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Schizophrenia is heterogeneous and often disabling a disease that affects 1% of the population. Current psychopharmacological treatment significantly eliminates the presence of positive symptoms (especially delusions and hallucinations) and partly also negative symptoms (social withdrawal or abulia). In contrast, the cognitive deficits associated both with schizophrenia and depression are only limitedly influenced by pharmacological treatment.The cognitive impairment represents an important part of schizophrenia symptomatology and it has a severe negative impact on patients' quality of life. In depression is the impairment milder but still significantly contributes to patients' daily functioning. The profound deficit was repeatedly documented in the area of declarative and working memory. In this study, we study the effectiveness of virtual environment rehabilitation program focused on declarative memory, working memory and attention in comparison to standard paper-pencil rehabilitation led by an occupational therapist.
Status | Completed |
Enrollment | 35 |
Est. completion date | January 1, 2021 |
Est. primary completion date | January 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Diagnosis of schizophrenia and other primary psychotic disorders or diagnosis of major depressive disorder according to International Classification of Diseases-11 Exclusion Criteria: - Severe visual impairment - Age over 60 years - Diagnosis of other psychiatric disorder than schizophrenia or major depressive disorder - Physical handicap preventing the participant from participating in virtual environment training - Refusal to sign an informed consent |
Country | Name | City | State |
---|---|---|---|
Czechia | Mental Health Center | Karviná |
Lead Sponsor | Collaborator |
---|---|
National Institute of Mental Health, Czech Republic |
Czechia,
Steingrimsdottir HS, Arntzen E. On the utility of within-participant research design when working with patients with neurocognitive disorders. Clin Interv Aging. 2015 Jul 23;10:1189-99. doi: 10.2147/CIA.S81868. eCollection 2015. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cognitive abilities measured by The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) | Baseline, 6-12 weeks, 12-24 weeks | ||
Secondary | Item performance in Virtual Supermarket Shopping Task | The data from individual sessions with Virtual Supermarket Shopping Task will be analyzed to see participants' progress. The variable item performance will be used = number of items to remember/ correctly collected items. | Baseline, 6-12 weeks |
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