Cost- Effectiveness Study of Brief Interventions for Mood and Anxiety Disorders

Not Applicable

Completed

• Conditions: Depressive Disorder; Anxiety Disorder
• Interventions: Other: Cognitive behavioral treatment/farmacotherapy intervention; Other: Treatment As Usual

• Registration Number: NCT01643642
• Lead Sponsor: Leiden University Medical Center

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-03
• Study First Submitted: 2011-09-08
• Study First Submitted QC: 2012-07-17
• Study First Posted: 2012-07-18
• Primary Completion: 2012-12
• Study Completion: 2012-12
• Status Verified: 2013-06
• Last Update Submitted: 2013-06-10
• Last Update Posted: 2013-06-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 182

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cognitive behavioral treatment/farmacotherapy intervention	Cognitive behavioral treatment/farmacotherapy intervention	Brief intervention; intake, cognitive behavioral treatment/farmacotherapy (SSRI) and ROM
Treatment As Usual	Treatment As Usual	Control group, TAU

Primary Outcome Measures

Name	Time	Method
Effectiveness of the intervention	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 Outcome Measures

Name	Time	Method
Cost-effectiveness intervention	approximately 3 years (start: march 2010).	Cost-effectiveness is explored by an open questionnaire Trimbos/iMTA Questionnaire for Cost Associated with Psychiatric Illness (TIC-P).; Additionally patient and therapist satisfaction about the intervention is explored.

Trial Locations

Locations (1)

Rivierduinen; 🇳🇱 South Holland, Netherlands