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Clinical Trials/NCT01913262
NCT01913262UnknownNot Applicable

IFH Depression Registry 2013

The Institute for Family Health1 site in 1 country1,000 target enrollmentStarted: March 2013Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
1,000
Locations
1
Primary Endpoint
Depression scores on PHQ-9 depression screening
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

This is an observational registry intended to track depression scores of patients over time in treatment.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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.

Exclusion Criteria

  • •Patients under the age of 18

Outcomes

Primary Outcomes

Depression scores on PHQ-9 depression screening

Time Frame: 16 weeks

Comparing depression scores for patients in treatment at initiation and after 16 weeks.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Virna Little

Senior Vice President of Psychosocial Services

The Institute for Family Health

Study Sites (1)

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