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Clinical Trials/NCT00057590
NCT00057590
Completed
Not Applicable

Outreach and Treatment for Depression in the Labor Force

Harvard Medical School (HMS and HSDM)1 site in 1 country590 target enrollmentMarch 2003
ConditionsDepression

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
Harvard Medical School (HMS and HSDM)
Enrollment
590
Locations
1
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This study will assess the effects of depression treatment on employee productivity. This study will also evaluate the impact of depression screening and outreach on employees' receptivity to treatment.

Detailed Description

This study is conducted in three phases. In the first phase, employees from various companies participate in an on-line Health Risk Assessment survey at a secure website. Those who display symptoms of depression participate in a brief telephone interview to confirm the depression diagnosis. In the second phase, depressed participants are randomly assigned to receive either intervention treatment or usual care for 18 months. The intervention consists of periodic telephone contact with a mental health clinician who provides education regarding depression and its treatment. Participants receiving the intervention are also provided with resources to obtain psychotherapy and/or pharmacotherapy. Those who do not seek treatment are monitored and supported. Participants in the usual care arm are informed of their possible depression and are encouraged to seek professional treatment. The final phase of the study involves data analysis and dissemination of aggregated results. Surveys and questionnaires are used to assess participants.

Registry
clinicaltrials.gov
Start Date
March 2003
End Date
TBD
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Harvard Medical School (HMS and HSDM)

Eligibility Criteria

Inclusion Criteria

  • Major depressive episode

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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