Postictal agitation agitation
Conditions
Interventions
Recorded music, with headphones, for 30 minutes directly before ECT and 12
minutes directly after ECT.
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing ECT treatment for depression 2. Hypnotic agent used is etomidate 3. Adult patients (>=18 years) 4. Sufficient understanding of the Dutch language 5. Written informed consent by patient or legal representative
Exclusion criteria
Exclusion criteria: 1. Significant impaired hearing 2. Severe neurological condition 3. Patients receiving ECT for treatment of schizophrenic disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is presence of postictal agitation as determined by the Richmond Agitation-Sedation Scale (RASS). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes are severity of PIA, duration of PIA, pretreatment anxiety, music listening behavior, duration of recovery (time spent in the recovery room), pre-, peri-, and post-treatment medication use, severity of depression, and cognitive impairment, measured by the Montreal Cognitive Assessment (MoCA) questionnaire. | — |
Countries
Netherlands
Contacts
Public ContactM.R. Koopmans
Erasmus MC, Universitair Medisch Centrum Rotterdam
Outcome results
None listed