None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged 19 years or older who have been diagnosed with cerebral infarction Individuals without a diagnosis of olfactory disorders, including sensorineural olfactory disorders or conductive olfactory disorders Individuals who are oriented and capable of communication Individuals without olfactory impairment and without a history of allergy to aromatherapy Individuals without allergic reactions to the essential oils used in this study Individuals not receiving pharmacological treatment for psychiatric disorders and not undergoing hormone therapy or essential oil therapy
Exclusion criteria
Exclusion criteria: Pregnant or breastfeeding women Individuals with suspected systemic infection Individuals with psychiatric disorders, drug or alcohol dependence, or those unable to understand the purpose and procedures of this clinical study Individuals with a history of allergic reactions to the essential oils used in this study Individuals deemed inappropriate for participation in the clinical study for any other reason, as determined by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fatigue score measured by the Visual Analog Scale (VAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Stress score measured by the Visual Analog Scale (VAS) | — |
Countries
Korea, Republic of
Contacts
Korea University Anam Hospital