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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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28 April 2013 |
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Main ID: |
NTR819 |
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Date of registration:
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21/11/2006 |
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Primary sponsor: |
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Public title:
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Collaborative Care: Depression in Occupational Care.
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Scientific title:
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The cost effectiveness of collaborative care for depressive disorder in the occupational health setting. - CC:DOC |
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Date of first enrolment:
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1/3/2007 |
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Target sample size:
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126 |
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Recruitment status: |
pending |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=819 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: Single; Control: Active; Group: Parallel; Type: [default]
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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M.C.
Vlasveld |
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Address:
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Netherlands institute of mental health and addiction, Da Costakade 45,
P.O. Box 725
3500 AS
Utrecht
The Netherlands |
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Telephone:
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+31 (0)30 2959303 |
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Email:
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mvlasveld@trimbos.nl |
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Affiliation:
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Name:
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C.M.
Feltz-Cornelis, van der |
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Address:
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Trimbos-institute - Netherlands Institute of Mental Health and Addiction, Department of Diagnosis en Treatment,
P.O. Box 725, Da Costakade 45
3500 AS
Utrecht
The Netherlands |
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Telephone:
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Email:
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cfeltz@trimbos.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: Employees on sick leave lasting between 6 and 52 weeks with major depressive disorder and who do not have the prospect of full return to work yet.
Exclusion criteria: Patients who are suicidal, psychotic or have dementia, as noticed by the company doctor, are excluded from this study. Also patients who are addicted to drugs or alcohol, as assessed by the MINI-interview, and patients who do not speak Dutch sufficiently to fill in the questionnaires, are excluded. Patients who are already receiving psychiatric treatment can be included in the study, in case of mutual agreement with the current care giver.
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Depressive disorders
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Intervention(s)
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The intervention follows a collaborative care model with adherence and compliance enhancing techniques, contracting, Problem Solving Treatment (PST), antidepressant medication prescribed by the consultant psychiatrist, and manual guided self help aimed at return to work and healthy lifestyle.
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Primary Outcome(s)
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The primary outcome measure is the extent of reduction in depressive symptoms, as measured by the PHQ-9.
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Secondary Outcome(s)
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The secondary outcome measure is time to return to work, which will be acquired upon inquiry with company doctor and patient and which refers to the duration of absence through illness until work is resumed.
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Secondary ID(s)
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2006/246
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ISRCTN78462860
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Source(s) of Monetary Support
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Foundation Reserves Voormalige Vrijwillige Ziekenfondsverzekering (RVVZ)
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