Effectiveness of Cultural Sensitive Collaborative Treatme... | NCT00664885

Studies
Effectiveness of Cultural Sensitive Collaborative Treatment of Depressed Chinese

NCT00664885

Sponsor

Mackay Memorial Hospital

Status

Completed

Last Update Posted

Jan 9, 2014Estimated

Enrollment

280Actual

Phase

Not Applicable

Conditions

Depression

Interventions

Culturally Sensitive Collaborative Treatment

Countries

Taiwan

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Jan 2014

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 2008

Primary Completion Date

Mar 2012Actual

Completion Date

Dec 2012Actual

First Submitted Date

Apr 18, 2008

First Submission Date that Met QC Criteria

Apr 22, 2008

First Posted Date

Apr 23, 2008Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jan 8, 2014

Last Update Posted Date

Jan 9, 2014Estimated

Name	Class
National Health Research Institutes, Taiwan	OTHER

Description Module

Brief Summary

This study is a randomized controlled trial to test whether Culturally Sensitive Collaborative Treatment (CSCT) would improve the outcome of depressed patients visiting non-psychiatric settings in Taiwan.

Detailed Description

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

280Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
CSCT	Experimental		Other: Culturally Sensitive Collaborative Treatment

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Culturally Sensitive Collaborative Treatment	Other	a collaborative care model, for treating depressed patients in general medical care	CSCT

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Depressed patients who receive CSCT have improved treatment outcomes compared to patients who receive usual care.		2wk,6 wk,10 wk,14 wk,18 wk,22wk,26wk

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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.

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

Not provided

Standard Ages

AdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

ID	Term
D001526	Behavioral Symptoms
D001519	Behavior