Anxiety
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical study. Experimental group: 45 individuals received 1 dropper bottle with 30mL of Saint Germain floral. The recommended intake was orally
Sponsors
Universidade Federal da Paraíba - Centro de Ciências Médicas
Universidade Federal da Paraíba - Centro de Ciências Médicas
Eligibility
Age
18 Years to 59 Years
Inclusion criteria
Inclusion criteria: Students of both sexes; aged between 18 and 59 years old; enrolled from the first to the fourth year of the Medicine or Dentistry course at Universidade Federal da Paraíba - UFPB
Exclusion criteria
Exclusion criteria: Participants who are undergoing flower therapy treatment during the research period; those who have any intolerance/allergy to alcoholic products; or pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to reduce the average level of anxiety in the final evaluation of the 8-week protocol, using the Trait Anxiety Inventory | — |
Secondary
| Measure | Time frame |
|---|---|
| Assess the level of quality of life using the World Health Organization Quality of Life instrument at the beginning and end of the study | — |
Countries
Brazil
Contacts
Public ContactAllanna Oliveira
Universidade Federal da Paraíba
Outcome results
None listed