Anxiety
Conditions
Interventions
This is a quasi-experimental, single-arm, before-and-after study, with the purpose of analyzing the profile and health outcomes of patients with anxiety who seek therapeutic support in the services of
Sponsors
Universidade Federal de Alfenas- MG
Universidade Federal de Alfenas- MG
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The study population will consist of people aged = 18 years, without gender restriction, who sought pharmaceutical care at a university pharmacy with a main complaint of anxiety or symptoms that characterize anxiety.
Exclusion criteria
Exclusion criteria: Patients who do not adhere for any reason to the treatment with the proposed herbal medicine during the three months of follow-up in this study will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to evaluate the satisfaction of patients with the use of Passiflora (humanistic outcome);It is expected with the economic outcome to evaluate the public expenditure of the treatment with Passiflora and pharmaceutical interventions ;It is expected to evaluate the effectiveness and safety of Passiflora sp. through clinical outcome | — |
Secondary
| Measure | Time frame |
|---|---|
| No outcomes are expected secondary | — |
Countries
Brazil
Contacts
Public ContactTiago Marques dos Reis
Universidade Federal de Alfenas- MG
Outcome results
None listed