Validation of the Spanish Version of the Clinically Useful Depression Outcome Scale (CUDOS) Scale

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

330 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-06-30

Study Completion Date

2011-11-30

Brief Summary

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The Clinically Useful Depression Outcome Scale (CUDOS) is a brief, self-administered instrument that not only evaluates depressive symptoms but also both functioning and quality of life. The assessment of patients´ perspective may provide valuable information that could be lost if relaying only on clinician evaluation. The purpose of this study is to achieve a psychometric validation into Spanish of the CUDOS scale in patients with major depression disorder in a primary care setting.

Detailed Description

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Conditions

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Unipolar Depression

Keywords

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psychometric validation major depressive disorder patient-reported outcome

Study Design

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Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Major Depressive Disorder Patients

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Major depression disorder diagnosis according to Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) criteria in the last 3 months
* Major depression disorder diagnosis according to Prime-MD criteria in the last 3 months

Exclusion Criteria

* Be unable to understand and comply with the study requirements as judged by the investigator
* Participation in another trial prior to enrolment into this study

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

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Spain

Other Identifiers

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NIS-NES-XXX-2011/1

Identifier Type: -

Identifier Source: org_study_id

Validation of the Spanish Version of the Clinically Useful Depression Outcome Scale (CUDOS) Scale

Study Results

Basic Information

Brief Summary

Detailed Description

Conditions

Keywords

Study Design

Study Groups

Major Depressive Disorder Patients

Eligibility Criteria

Inclusion Criteria

Exclusion Criteria

Sponsors

AstraZeneca

Responsible Party

Locations

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Countries

Other Identifiers

NIS-NES-XXX-2011/1