Toetsing van een geïntegreerd behandelprotocol voor patiënten met een bipolaire stoornis en eencomorbide borderline persoonlijkheidskenmerken. Een randomized clinical trial.
- Conditions
- bipolar disorder, borderline personality disorderbipolaire stoornis, borderline persoonlijkheidsstoornis
- Registration Number
- NL-OMON25406
- Lead Sponsor
- VU University Medical Center, dept. of Psychiatry, Amsterdam
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
• age 18 – 65
• diagnosis of bipolar disorder-I, bipolar disorder-II, or bipolar disorder-NOS
Exclusion Criteria
• hospitalization for suicide risk
• current severe depressive episode (IDS-SR > 38)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcomes will be the frequency and severity of manic and depressive episodes as well as symptoms, course and burden of borderline personality features.
- Secondary Outcome Measures
Name Time Method Secondary outcomes will be quality of life, utilizing mental healthcare and psychopathologic symptoms not related to bipolar disorder or borderline personality features.