Outreach and Treatment for Depression in the Labor Force

Sponsor
Harvard Medical School (HMS and HSDM) (Other)
Overall Status
Completed
CT.gov ID
NCT00057590
Collaborator
National Institute of Mental Health (NIMH) (NIH)
590
1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Care manager outreach and monitoring
N/A

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.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Primary Purpose:
Treatment
Official Title:
Outreach and Treatment for Depression in the Labor Force
Study Start Date :
Mar 1, 2003

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Major depressive episode

    • Employed

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Harvard Medical School Boston Massachusetts United States 02115

    Sponsors and Collaborators

    • Harvard Medical School (HMS and HSDM)
    • National Institute of Mental Health (NIMH)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00057590
    Other Study ID Numbers:
    • R01MH061941
    • R01MH061941
    • DSIR 82-SEDX
    First Posted:
    Apr 8, 2003
    Last Update Posted:
    May 6, 2013
    Last Verified:
    May 1, 2013
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 6, 2013