Generalized anxiety disorder
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with GAD (diagnosed according to DSM-5) who participated in "A placebo-controlled, randomized, double-blind, multicenter study to evaluate the efficacy and safety of venlafaxine in Japanese outpatients with generalized anxiety disorder (Study B2411367)" via a clinical trial information website and meet the following criteria will be included in analyses. 1.Voluntarily consented to participate in this study by electronic means
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endpoint 1: Awareness of GAD and medical care-seeking behavior until diagnosis Endpoint 2: Symptoms of GAD at trial entry Endpoint 3: Visits to the clinical trial site and diagnosis Endpoint 4: Situation from after the end of the clinical trial to the present Endpoint 5: Efforts needed to promote disease awareness | — |
Countries
Japan
Contacts
3H Medi Solution Inc. Patient Recruitment Group