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Effectiveness of a Cognitive Remediation Intervention Based on Virtual Reality for Promotion of Cognitive Functioning and Participation in Daily Life Among Persons With Affective Disorder

Effectiveness of a Cognitive Remediation Intervention Based on Virtual Reality for Promotion of Cognitive Functioning and Participation in Daily Life Among Persons With Affective Disorder

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04288609
Enrollment
40
Registered
2020-02-28
Start date
2020-03-31
Completion date
2020-12-01
Last updated
2020-02-28

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

Conditions

Affective Disorder

Keywords

affective disorder

Brief summary

The purpose of this study is to test the efficacy of remedial cognitive intervention using The Functional Brain Trainer VR (FBT, Intendo ©) to improve cognitive functioning, participation in daily life occupations, and functional capacity in the field of IADL among people with affective disorders receiving inpatient and daycare mental-health services.

Detailed description

This study is an experimental study, in a pre-post design with a control group, the sampling is convenience. The study will include 40 people aged 18-60 with a diagnosis of Affective disorder based on DSM-5. Inclusion criteria: age 18-60, Diagnosis of Major Depression or Bipolar disorder based on DSM-5; Mood stabilizing medication for at least 2 weeks, Exclusion criteria: Neurological disorders and neurodevelopmental conditions in addition to mental health diagnosis; Physical disability in addition to mental health conditions; Psychotic state; active substance abuse; custodian. They will be recruited from active inpatient and daycare wards of the Geha Mental Health Center, Israel and will be randomly allocated into two groups: experimental and control. An experimental group will attend 6 VR based cognitive remediation sessions of 30 minutes for training response inhibition, self-initiation, cognitive flexibility, sustained attention, divided attention, working memory, planning, persistence. The control group will complete 6 sessions of 30 minutes of low-tech (paper and pencil tasks) remedial training of the same cognitive components. These in addition to routine care. The evaluation for symptoms severity, cognition, functional capacity and participation in daily life activities will be conducted at the beginning of the study and after about 4 weeks.

Interventions

OTHERIntendu

Cognitive remediation using VR adaptive platform for response inhibition, self-initiation, cognitive flexibility, sustained attention, divided attention, working memory, planning, persistence.

OTHERPaper and Pencil cognitive remediation training

Cognitive remediation using paper and pencil tasks for response inhibition, self-initiation, cognitive flexibility, sustained attention, divided attention, working memory, planning, persistence.

Sponsors

Tel Aviv University
CollaboratorOTHER
Geha Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

single

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-60, * Diagnosis of Major Depression or Bipolar disorder based on DSM-5; * Mood stabilizing medication for at least 2 weeks,

Exclusion criteria

* Neurological disorders and neuro-developmental conditions in addition to mental health diagnosis; * Physical disability in addition to mental health conditions; * Psychotic state; * active substance abuse; * custodian

Design outcomes

Primary

MeasureTime frameDescription
The Observed Tasks of Daily Living - Revised3 weeksAssessment of Functional capacity, score range 1 (dependent in the performance of daily life activities) up to 26 (fully independent in the performance of the daily life activities)
Adults Subjective Assessment of Participation3 weeksQuestionnaire for assessment of participation in daily life activities: number of participated activities (from 1 to 52, the higher number indicates higher number of participated activities) and frequency of the participation (range from 1 indicates low frequency of participation up to 7 - higher frequency of the participation)

Secondary

MeasureTime frameDescription
The Neurobehavioral Cognitive Status Examination3 weeksExamination cognitive components of attention language, spatial skills, memory, calculations and reasoning. The score range for different sub-tests from 1 up to 4, 6, 8 or 12, with higher score indicates better cognitive functioning
Trail Making Test A & B3 weeksMeasure of cognitive flexibility and psycho-motor processing speed, the score is a time needed for the test completion, less time that needed indicates better cognitive functioning
Category Fluency Test3 weeksAssessment of language fluency, the score is a number of produced words, the higher the number, the better cognitive fluency
Hamilton Depression Rating Scale Questionnaire3 weeksAssessment of the depressive symptoms, the higher score indicates more severe depressive symptoms.

Contacts

Primary ContactGilad Eger, PhD
giladeg1@clalit.org.il+972523520180
Backup ContactDovrat Cohen, BOT
dovratco@clalit.org.il+972526763854

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026