- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04598906
Ecologically Valid Virtual Tasks vs Paper-pencil Methods in Cognitive Rehabilitation in Patients With Schizophrenia and Depression
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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study compares effectiveness of the virtual environment cognitive rehabilitation program with standard paper-pencil approach in within-subject design.
Participants with a diagnosis of schizophrenia, schizoaffective disorder or major depressive disorder will undergo a baseline assessment of cognition.
The participants will be at the baseline randomly assigned to each condition: virtual environment rehabilitation or paper-pencil rehabilitation. Then they will participate in 10-15 sessions (30-45 minutes) once or twice a week.
All participants will undergo retest assessment of cognition.
After completion of the first program the participants will be assigned to the different condition: to paper-pencil or virtual environment rehabilitation. After 10-15 sessions in the second condition the participants will once more undergo retest assessment of cognition.
Within-subject design is an effective tool in the development of scientifically proven treatment tools. This approach allows to obtain reliable information about the effectiveness of the method and to examine the influences of other variables (Steingrimsdottir and Arntzen 2015). This study will allow to get credible information on the importance of using the virtual environment in the context of cognitive rehabilitation in patients with schizophrenia and depression.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Karviná, Czechia, 733 01
- Mental Health Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Virtual environment rehabilitation - Paper-pencil rehabilitation
The participants in this arm completes Virtual environment rehabilitation as the first condition and then crossover to Paper-pencil rehabilitation.
|
The participants attended 10-15 computer sessions during 6-12 weeks.
Each session lasted 30 minutes and consisted of the set of virtual environment tasks (Shooting Range,Virtual Supermarket Shopping Task and Objects).
Shooting range demands differentiation of targets from non-targets and focuses on training of selective attention, psychomotor speed and inhibition control.
Virtual Supermarket Shopping requires memorizing the shopping list and searching for products in the supermarket area.
Objects requires memorizing of the spatial and temporal context while searching for objects.
The participants in the paper-pencil rehabilitation attended 10-15 paper pencil sessions for 6-12 weeks.
Each session lasted 45 minutes.
Each paper-pencil session starts with a warm-up game.
The session continues with a set of paper-pencil tasks focused on attention, fine motor skills, recall, short-term and long-term memory, verbal fluency, visual search, cognitive flexibility, abstraction and executive functions, numerical abilities.
The tasks are adapted according to the participant´s abilities.
|
|
Experimental: Paper-pencil rehabilitation - Virtual environment rehabilitation
The participants in this arm completes Paper-pencil rehabilitation as the first condition and then crossover to Virtual environment rehabilitation.
|
The participants attended 10-15 computer sessions during 6-12 weeks.
Each session lasted 30 minutes and consisted of the set of virtual environment tasks (Shooting Range,Virtual Supermarket Shopping Task and Objects).
Shooting range demands differentiation of targets from non-targets and focuses on training of selective attention, psychomotor speed and inhibition control.
Virtual Supermarket Shopping requires memorizing the shopping list and searching for products in the supermarket area.
Objects requires memorizing of the spatial and temporal context while searching for objects.
The participants in the paper-pencil rehabilitation attended 10-15 paper pencil sessions for 6-12 weeks.
Each session lasted 45 minutes.
Each paper-pencil session starts with a warm-up game.
The session continues with a set of paper-pencil tasks focused on attention, fine motor skills, recall, short-term and long-term memory, verbal fluency, visual search, cognitive flexibility, abstraction and executive functions, numerical abilities.
The tasks are adapted according to the participant´s abilities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Cognitive abilities measured by The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
Time Frame: Baseline, 6-12 weeks, 12-24 weeks
|
Baseline, 6-12 weeks, 12-24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Item performance in Virtual Supermarket Shopping Task
Time Frame: Baseline, 6-12 weeks
|
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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Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- VRremediation
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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