F00
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - dementia - agitated behaviour - permanent inpatient nursing care - documented indication-related medication
Exclusion criteria
Exclusion criteria: - short term nursing care / day care - no prescription of indication-related medicaion - known allergy against essential oils - medical condition (process of dying, severe psychological or cognitive impairments)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| quantitative: clinical benefit - decline of agitation (Cohen-Mansfield Agitation Inventory, Neuropsychiatric Inventory NH) over 12 weeks every 14 days (8 weeks intervention phase plus 4 weeks follow-up) qualitative: process evaluation and feasibility analysis (qualitative interviews) after intervention phase | — |
Secondary
| Measure | Time frame |
|---|---|
| quantitative: management of side effects (documentation sheet) after each session qualitative: decline of indication-related medication (treatment plan)(parallel with questionnaires) | — |
Countries
Germany
Contacts
Institut für Allgemeinmedizin & Interprofessionelle Versorgung, Universitätsklinikum Tübingen