Epidemiology of Treatment Resistant Depression in Taiwan
2 other identifiers
observational
8,356
0 countries
N/A
Brief Summary
The purpose of this study is to assess the epidemiology of Treatment Resistant Depression (TRD) in the nationally insured population in Taiwan including incidence, duration of clinical episodes, and prevalence by age and sex.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2015
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 29, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 18, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
February 18, 2016
CompletedFirst Submitted
Initial submission to the registry
February 22, 2016
CompletedFirst Posted
Study publicly available on registry
February 25, 2016
CompletedOctober 28, 2024
October 1, 2024
5 months
February 22, 2016
October 24, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Incidence Percentage of Participants with Treatment Resistant Depression
The percentage of beneficiaries of Taiwan's health insurance plan who developed treatment resistant depression during 2005
Approximately 8 Years
Prevalence Percentage of Participants with Treatment Resistant Depression
Approximately 8 Years
Duration of an episode of Depression
Time from onset of depression to cessation of depression visits and medications.
Approximately 8 Years
Secondary Outcomes (3)
Healthcare costs
Approximately 8 Years
Number of Participants With Comorbidities
Approximately 8 Years
Medications used by Participants with Treatment Resistant Depression
Approximately 8 Years
Study Arms (1)
Taiwan Participants with Treatment Resistant Depression
Taiwan participants with Depression will be followed up to 8 years for incidence and duration of treatment resistant depression.
Eligibility Criteria
Adults aged 18 and older are randomly sampled from the National Health Insurance Research Database (NHIRD).
You may qualify if:
- Participants with a diagnosis of a depressive disorder including dysthymic disorder (International Classification of Diseases \[ICD\]-9 codes 296 depression-related, 300.4, 311) and Major Depressive Disorder (ICD-9 296.2, 296.3) will be followed through December 31, 2013
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Janssen Research & Development, LLClead
- Elysia Groupcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Janssen Research & Development, LLC Clinical Trial
Janssen Research & Development, LLC
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 22, 2016
First Posted
February 25, 2016
Study Start
September 29, 2015
Primary Completion
February 18, 2016
Study Completion
February 18, 2016
Last Updated
October 28, 2024
Record last verified: 2024-10