IFH Depression Registry 2013
1 other identifier
observational
1,000
1 country
1
Brief Summary
This is an observational registry intended to track depression scores of patients over time in treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
1 active site
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
March 1, 2013
CompletedFirst Submitted
Initial submission to the registry
July 30, 2013
CompletedFirst Posted
Study publicly available on registry
August 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2015
CompletedAugust 1, 2013
July 1, 2013
2 years
July 30, 2013
July 31, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Depression scores on PHQ-9 depression screening
Comparing depression scores for patients in treatment at initiation and after 16 weeks.
16 weeks
Study Arms (1)
IFH Patients on Depression Registry
Patients at the Institute for Family Health who have a diagnosis of depression active on their problem list or have had a diagnosis of depression used as an encounter diagnosis in the past year or patients with a PHQ-9 score greater than or equal to 10.
Interventions
Standard behavioral treatment (e.g. problem solving therapy, cognitive behavioral treatment)
Eligibility Criteria
Community health patients in behavioral health treatment
You may qualify if:
- Patients with PHQ-9 score greater than or equal to 10, have a depression diagnosis active on the problem list, or have had a depression encounter diagnosis used in the past year, and are in behavioral health treatment at the Institute.
You may not qualify if:
- Patients under the age of 18
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Institute for Family Health
New York, New York, 10003, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 4 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Vice President of Psychosocial Services
Study Record Dates
First Submitted
July 30, 2013
First Posted
August 1, 2013
Study Start
March 1, 2013
Primary Completion
March 1, 2015
Last Updated
August 1, 2013
Record last verified: 2013-07