Memoral efficacy on prevention of memory impairment
Not Applicable
- Conditions
- ECT-induced memory impairment.Organic amnesic syndrome, not induced by alcohol and other psychoactive substances
- Registration Number
- IRCT201102072232N2
- Lead Sponsor
- Behavioural Sciences Research Center of Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Age range of 15-65; diagnosis of Major Depressive Disorder or Bipolar Disorder; informed acceptance for participating in the study; prescription of at least 4 sessions of ECT by psychiatrist. Exclusion criteria: Dementia or mental retardation; discontinuation of ECT before 4 sessions; refusing cooperation after primary acceptance; delirium during intervention
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Memory. Timepoint: Befor first and fourth ECT session, one and two months after the last session of ECT. Method of measurement: Completion of questionnaire.
- Secondary Outcome Measures
Name Time Method Memoral side effect. Timepoint: Before first and fourth ECT session, one an two months after the last session of ECT. Method of measurement: Questionaire.