Skip to content

Reconsolidation intervention for burnout.

Reconsolidation intervention for burnout. - #burnout

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51177
Enrollment
12
Registered
2020-12-31
Start date
2022-06-09
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

panic disorder | burnout

Interventions

A single reactivation of panic symptoms at work through hyperventilation provocation, followed by the oral administration of 40 mg of the noradrenergic *-blocker propranolol.

Sponsors

TNO
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
Our primary output will be the decrease in frequency and severity of panic symptoms, from screening to post-treatment and follow-up.

Secondary

MeasureTime frame
Our secondary output will be the decrease in the levels of burnout, from screening to post-treatment and follow-up.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)