Reconsolidation intervention for burnout.
Completed
- Conditions
- panic disorder | burnout10002861
- Registration Number
- NL-OMON51177
- Lead Sponsor
- TNO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 12
Inclusion Criteria
1. aged between 18 and 65 years;
2. a score of > 8 on the Panic Disorder Severity Scale;
3. a score of > 2.79 on both the core symptoms and secondary symptoms of the
work-related version of the Burnout Assessment Tool;
4. a score of at least 4 on the panic and anxiety item of the BAT.
Exclusion Criteria
1. other relevant treatment for panic symptoms or burnout within 3 months
before start of the study;
2. life-time psychosis;
3. depression;
4. current state of asthma or COPD, which necessitates medication use;
5. cardiovascular diseases or irregular heartbeat;
6. hypotension or hypertension;
7. pregnancy or breastfeeding;
8. epilepsy;
9. any medication contra-indicative of the use of propranolol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Our primary output will be the decrease in frequency and severity of panic<br /><br>symptoms, from screening to post-treatment and follow-up.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Our secondary output will be the decrease in the levels of burnout, from<br /><br>screening to post-treatment and follow-up.</p><br>