NCT00984685

Brief Summary

The purpose of the study is to identify the barriers for effective treatment of depression, specifically whether modified CHIS Scale is a valid tool for identifying the high risk patients for depression.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2009

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2009

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

September 24, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 25, 2009

Completed
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2009

Completed
Last Updated

September 25, 2009

Status Verified

September 1, 2009

Enrollment Period

1 month

First QC Date

September 24, 2009

Last Update Submit

September 24, 2009

Conditions

Depression

Outcome Measures

Primary Outcomes (1)

  • proportion of anti-depressant prescriptions filled

    August 1, 2008 through July 31, 2009

Study Arms (1)

depression

Patients diagnosed with depression before April 15, 2009

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with the diagnosis of depression in theprimary care clinic

You may qualify if:

  • Diagnosis of depression before April 15, 2009
  • At least one visit since April 15, 2008
  • Age 18+

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Scranton Temple Residency Program

Scranton, Pennsylvania, 18510, United States

RECRUITING

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • John R Guzek, MD

    Scranton-Temple Residency Program

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 24, 2009

First Posted

September 25, 2009

Study Start

August 1, 2009

Primary Completion

September 1, 2009

Study Completion

October 1, 2009

Last Updated

September 25, 2009

Record last verified: 2009-09

Locations

US(1)