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Main
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Note: This record shows only 22 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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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT00664885 |
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Date of registration:
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18/04/2008 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effectiveness of Cultural Sensitive Collaborative Treatment of Depressed Chinese
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Scientific title:
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Effectiveness of Cultural Sensitive Collaborative Treatment of Depressed Chinese in Primary Care |
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Date of first enrolment:
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January 2008 |
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Target sample size:
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280 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00664885 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients who attend non-psychiatric clinics at the above site.
- Patients with Major Depressive Disorder (MDD), defined as a positive screen using
the PHQ-9, confirmed with the SCAN interview.
- Men or women aged 18 or older.
- Able to participate in a clinical diagnostic interview in either Mandarin or
Fukienese dialects.
- Individuals who are willing to be followed up concerning their depression symptoms.
- Individuals who have completed a written consent form.
Exclusion Criteria:
- Women who are pregnant, breast-feeding, or planning pregnancy within the next year.
- Patients with serious suicidal risk.
- Patients with unstable medical illnesses.
- Clinical or laboratory evidence of hypothyroidism.
- Patients with comorbid severe mental disorders
- Patients with history of treatment by a psychiatrist in the past 4 months.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Depression
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Intervention(s)
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Other: Culturally Sensitive Collaborative Treatment
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Primary Outcome(s)
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Depressed patients who receive CSCT have improved treatment outcomes compared to patients who receive usual care.
[Time Frame: 2wk,6 wk,10 wk,14 wk,18 wk,22wk,26wk]
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Secondary ID(s)
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NHRI-EX97-9706PI
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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