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Clinical Trials/NCT01643642
NCT01643642
Completed
Not Applicable

A Efficacy and Cost-effectiveness Study of a Brief Interventions for Mood and Anxiety Disorders: Brief Intake, Treatment and Routine Outcome Monitoring (ROM)

Leiden University Medical Center1 site in 1 country182 target enrollmentMarch 2010
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ConditionsDepressive DisorderAnxiety Disorder

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depressive Disorder
Sponsor
Leiden University Medical Center
Enrollment
182
Locations
1
Primary Endpoint
Effectiveness of the intervention
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

This study compares both clinical effectiveness and cost-effectiveness of a brief, intensified therapy and diagnostic method for patients with mood and/or anxiety disorders with Treatment As Usual (TAU) at five outpatient Mental Healthcare Centers in the Netherlands.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
December 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Leiden University Medical Center
Responsible Party
Principal Investigator
Principal Investigator

D. Meuldijk

PhD Student

Leiden University Medical Center

Eligibility Criteria

Inclusion Criteria

  • •Male of female adolescents
  • •Adolescents aged between 18 to 65 year
  • •Adolescents main complaint: Mild to moderate anxiety and/or mood disorders with or without psychiatric and/or somatic co-morbidity
  • •Adolescents with proper understanding of the Dutch language.

Exclusion Criteria

  • •Adolescents with current psychotic or bipolar traits,
  • •Adolescents with homicidal or suicidal risk
  • •Adolescents with severe social disfunctioning
  • •No proper understanding of the Dutch language

Outcomes

Primary Outcomes

Effectiveness of the intervention

Time Frame: approximately 3 years (start: march 2010).

Effectiveness of the intervention is investigated by the main questionnaires: Web Screening Questionnaire (WSQ) and Brief Symptom Inventory (BSI) as conducted by ROM

Secondary Outcomes

  • Cost-effectiveness intervention(approximately 3 years (start: march 2010).)

Study Sites (1)

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