Anxiety
Conditions
Interventions
This is a mixed-methods study using an embedded design, with quantitative predominance, in which 38 participants will take part. The primary approach consists of a non-controlled intervention study wi
Sponsors
Departamento de Enfermagem
Universidade Federal do Rio Grande do Norte
Eligibility
Age
19 Years to No maximum
Inclusion criteria
Inclusion criteria: Participants of either sex; age = 19 years; with a history of mild to moderate anxiety whether diagnosed or self-reported; with no history of psychiatric disorders and no allergy to lavender or other scents
Exclusion criteria
Exclusion criteria: Presence of severe anxiety; olfactory disorders or hearing impairments that may prevent the patient from hearing the audio used during the image guided procedure properly
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that there will be a reduction in anxiety levels, as measured by the Beck Anxiety Inventory | — |
Secondary
| Measure | Time frame |
|---|---|
| We expect to observe an improvement in well-being as measured by the World Health Organization’s Well-being Index, as well as participants’ perceptions and experiences regarding the intervention, as gathered through semi-structured interviews | — |
Countries
BR
Contacts
Public ContactRodrigo Neves Dantas
Rodrigo Assis Neves Dantas
Outcome results
None listed