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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00885014
Other study ID # NCUPsychiatry002
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received April 20, 2009
Last updated March 15, 2012
Start date April 2009
Est. completion date September 2011

Study information

Verified date March 2012
Source Kyoto University
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of the study is to examine the effectiveness of telephone cognitive-behavioral therapy for subthreshold depression and presenteeism in workplace, in comparison with treatment-as-usual (TAU) (which is minimal contact through Employers Assistance Program (EAP)).


Recruitment information / eligibility

Status Completed
Enrollment 118
Est. completion date September 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 57 Years
Eligibility Inclusion Criteria:

- Age 20-57 at study entry [because the retirement age is usually 60, we have to recruit the patients well before 60 in order to allow time for follow-up]

- Men and women

- Currently employed full-time (either regular or temporary) by the business company

- Expected to be employed full-time for 2 years after screening

- K6 scores greater than or equal to 9 (or 10) at screening

- BDI2 scores greater than or equal to 10 at 2nd screening (Composite International Diagnostic Interview (CIDI) interview)

Exclusion Criteria:

- Part-time employees

- Sick leave for 6 or more days for a physical or mental condition in the past month

- Expected to be on pregnancy leave, maternity leave or nursing leave within 2 years after screening

- Current treatment for a mental health problem from a mental health professional

- Major depressive episode in the past month, as ascertained by CIDI [We do not exclude dysthymia or major depression in partial remission]

- Lifetime history of bipolar disorder, as ascertained by CIDI

- Any substance dependence in the past 12 months, as ascertained by CIDI. [We do not exclude substance abuse.]

- Any other current mental disorder if it constitutes the predominant aspect of the clinical presentation and requires treatment not offered in the project

- Those who have already received the telephone CBT in the pilot runs

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
CBT
Telephone cognitive-behavioral therapy
EAP
Employees Assistance Program

Locations

Country Name City State
Japan Nagoya City University Nagoya Aichi

Sponsors (2)

Lead Sponsor Collaborator
Kyoto University Nagoya City University

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Depression severity as measured by Beck Depression Inventory-II (BDI2) 4 months post-randomization No
Primary Work performance as measured by the Health and Work Performance Questionnaire (HPQ) "effective hours worked" for the past month 4 months post-randomization No
Secondary Depression severity as measured by Kessler Scale (K6) 4 months post-randomization No
Secondary Client satisfaction as measured by Visual Analogue Scale (VAS) 4 months post-randomization No
Secondary Depression severity as measured by BDI2 and K6 15 months post-randomization No
Secondary Work performance as measured by HPQ and by job retention 15 months post-randomization No
Secondary Client satisfaction as measured by VAS 15 months post-randomization No
Secondary Use of EAP services and other health services 15 months post-randomization No
Secondary Suicidal attempt and/or hospitalization (physical or mental) 15 months post-randomization Yes
Secondary Time to incident major or minor depressive episode 15 months post-randomization No
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