Auriculotherapy
Conditions
Interventions
The clinical trial will consist of two groups to control the study: the placebo group (will receive points that do not influence anxiety) and the intervention group (will receive the treatment conside
E02.190
Sponsors
Universidade Federal de Sergipe
Universidade Federal de Sergipe
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: students enrolled in Medicine, Nursing and Physiotherapy; schedule time for those scheduled; be over 18 years old.
Exclusion criteria
Exclusion criteria: pregnant women; perform some other pharmacological or non-pharmacological treatment for anxiety; people with previous negative experiences in the practice of auriculotherapy; withdrawal or refusal to continue participating in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of symptoms and anxiety levels, verified through the practice of auriculotherapy for 8 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement of anxiety levels and in relation to studies, after the 2nd session of auriculotherapy. | — |
Countries
Brazil
Contacts
Public ContactAnne Santos
Universidade Federal de Sergipe
Outcome results
None listed