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E-Compared-CH: Comparative Effectiveness Research on Internet-based Depression Treatment - Swiss Trial (E-COMPARED_CH)

Primary Purpose

Depressive Disorder, Major

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Blended CBT
Treatment as usual
Sponsored by
University of Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder, Major focused on measuring Psychotherapy, Comparative Effectiveness Research, Randomized Controlled Trial, Secondary Care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Being 18 years of age or older
  • Meet DSM-IV diagnostic criteria for MDD confirmed by MINI International Neuropsychiatric Interview version 5.0
  • Informed Consent
  • Having access to a PC and Internet connection
  • Having a Smartphone that is compatible with the mobile component of the intervention
  • Understanding of the German language spoken and written

Exclusion Criteria

  • Current high risk for suicide according to the MINI Interview section C
  • Serious psychiatric co-morbidity: substance dependence, bipolar affective disorder, psychotic illness, obsessive compulsive disorder, as established at the MINI interview
  • Currently receiving psychological treatment for depression
  • Being unable to comprehend the spoken and written language (German)
  • Not having access to a PC and fast Internet connection (i.e. broadband or comparable).
  • Not having a Smartphone that is compatible with the mobile component of the intervention that is offered or not willing to carry a Smartphone during the duration of treatment

Sites / Locations

  • Sanatorium Kilchberg
  • Department of Clinical Psychology and Psychotherapy

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Blended CBT

Treatment as usual

Arm Description

Internet based blended CBT depression treatment combines individual face-to-face cognitive behavioural therapy (CBT) with CBT delivered through an Internet based treatment platform with mobile phone components. The core components of the CBT treatment are: (1) psychoeducation, (2) behavioural activation, (3) cognitive restructuring, and (4) relapse prevention.

Treatment as usual (TAU) is defined as the routine care that subjects receive when they are diagnosed with depression in the secondary care system. The investigators will not interfere with treatment as usual but they will monitor carefully which health care services are utilized by usual care patients using patient records and through self-report.

Outcomes

Primary Outcome Measures

Patient Health Questionnaire-9 (PHQ-9)

Secondary Outcome Measures

Assessment of Quality of Life (AQoL-6D)
Quick Inventory of Depressive Symptomatology Self-Report (QIDS-16-SR)
MINI International Neuropsychiatric Interview (M.I.N.I; Ackenheil et al., 1999)
EuroQoL (EQ-5D-5L; Herdman et al., 2011)
Questionnaires on Costs Associated with Psychiatric Illness (TiC-P; Hakkaart-van Rooijen, van Straten, Donker, Tiemens, 2002)
Client Satisfaction Questionnaire (CSQ-8; Nguyen, Attkinson, & Stegner, 1983)
System Usability Scale (SUS; Brooke, 1996)
Patient Health Questionnaire-9 (PHQ-9)

Full Information

First Posted
April 2, 2015
Last Updated
September 20, 2017
Sponsor
University of Bern
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1. Study Identification

Unique Protocol Identification Number
NCT02410616
Brief Title
E-Compared-CH: Comparative Effectiveness Research on Internet-based Depression Treatment - Swiss Trial
Acronym
E-COMPARED_CH
Official Title
European Comparative Effectiveness Research on Internet-based Depression Treatment - Swiss Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
July 2017 (Actual)
Study Completion Date
July 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Bern

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To compare the clinical and cost-effectiveness of blended Cognitive Behavioural Therapy (CBT) for adults with major depressive disorder (MDD) with treatment as usual (TAU) in Swiss patients in secondary care
Detailed Description
Background Depression is a common mental disorder with a negative impact on mental well-being, quality of life, and social and work-related functioning both in the short and longer term. Additionally, depression is associated with increased morbidity, mortality, health care utilization and health care costs. On a population level, depression is one of the most costly diseases. The economic costs of depression were estimated at €136.3 billion (EU25) in 2010 in the EU and are still rising. European health care systems face the challenge of improving access to cost-effective treatments while simultaneously working to sustain budgetary stability in times of economic austerity. Internet-based depression treatment appears a very promising alternative to current routine depression treatment strategies. Meta-analyses have demonstrated the clinical effectiveness and potential cost-effectiveness of Internet-based treatment for depression in controlled research setting. Internet-based treatment thus has the potential to keep depression treatment affordable, as it enables mental health care providers to reach out to large populations needing depression treatment at a better cost-effectiveness than those of standard treatment as usual (TAU), but with similar levels of clinical efficacy and quality of care. The trials will be conducted in 8 European countries. Objective To compare the clinical and cost-effectiveness of blended CBT and TAU in secondary care Methods In Switzerland, a randomized-controlled trial will be carried out in secondary care, comparing the clinical and cost-effectiveness of CBT and TAU for adults with major depressive disorder (MDD). Respondents will be followed until 12 months after baseline (measures will be taken at BL, 12 weeks, 18 weeks, 6 months and 12 months).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder, Major
Keywords
Psychotherapy, Comparative Effectiveness Research, Randomized Controlled Trial, Secondary Care

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Blended CBT
Arm Type
Experimental
Arm Description
Internet based blended CBT depression treatment combines individual face-to-face cognitive behavioural therapy (CBT) with CBT delivered through an Internet based treatment platform with mobile phone components. The core components of the CBT treatment are: (1) psychoeducation, (2) behavioural activation, (3) cognitive restructuring, and (4) relapse prevention.
Arm Title
Treatment as usual
Arm Type
Active Comparator
Arm Description
Treatment as usual (TAU) is defined as the routine care that subjects receive when they are diagnosed with depression in the secondary care system. The investigators will not interfere with treatment as usual but they will monitor carefully which health care services are utilized by usual care patients using patient records and through self-report.
Intervention Type
Behavioral
Intervention Name(s)
Blended CBT
Intervention Description
Internet based blended CBT depression treatment combines individual face-to-face cognitive behavioural therapy (CBT) with CBT delivered through an Internet based treatment platform with mobile phone components. The core components of the CBT treatment are: (1) psychoeducation, (2) behavioural activation, (3) cognitive restructuring, and (4) relapse prevention.
Intervention Type
Behavioral
Intervention Name(s)
Treatment as usual
Intervention Description
Treatment as usual (TAU) is defined as the routine care that subjects receive when they are diagnosed with depression in the secondary care system. The investigators will not interfere with treatment as usual but they will monitor carefully which health care services are utilized by usual care patients using patient records and through self-report.
Primary Outcome Measure Information:
Title
Patient Health Questionnaire-9 (PHQ-9)
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
Assessment of Quality of Life (AQoL-6D)
Time Frame
Baseline, 12 weeks, 18 weeks, 6 months, and 12 months
Title
Quick Inventory of Depressive Symptomatology Self-Report (QIDS-16-SR)
Time Frame
Baseline, 12 weeks, 18 weeks, 6 months, and 12 months
Title
MINI International Neuropsychiatric Interview (M.I.N.I; Ackenheil et al., 1999)
Time Frame
Baseline, 18 weeks, and 12 months
Title
EuroQoL (EQ-5D-5L; Herdman et al., 2011)
Time Frame
Baseline, 12 weeks, 18 weeks, 6 months, and 12 months
Title
Questionnaires on Costs Associated with Psychiatric Illness (TiC-P; Hakkaart-van Rooijen, van Straten, Donker, Tiemens, 2002)
Time Frame
Baseline, 12 weeks, 18 weeks, 6 months, and 12 months
Title
Client Satisfaction Questionnaire (CSQ-8; Nguyen, Attkinson, & Stegner, 1983)
Time Frame
12 weeks, and 18 weeks
Title
System Usability Scale (SUS; Brooke, 1996)
Time Frame
12 weeks, and 18 weeks
Title
Patient Health Questionnaire-9 (PHQ-9)
Time Frame
Baseline, 12 weeks, 6 months, and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Being 18 years of age or older Meet DSM-IV diagnostic criteria for MDD confirmed by MINI International Neuropsychiatric Interview version 5.0 Informed Consent Having access to a PC and Internet connection Having a Smartphone that is compatible with the mobile component of the intervention Understanding of the German language spoken and written Exclusion Criteria Current high risk for suicide according to the MINI Interview section C Serious psychiatric co-morbidity: substance dependence, bipolar affective disorder, psychotic illness, obsessive compulsive disorder, as established at the MINI interview Currently receiving psychological treatment for depression Being unable to comprehend the spoken and written language (German) Not having access to a PC and fast Internet connection (i.e. broadband or comparable). Not having a Smartphone that is compatible with the mobile component of the intervention that is offered or not willing to carry a Smartphone during the duration of treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Berger, PhD
Organizational Affiliation
University of Bern
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sanatorium Kilchberg
City
Kilchberg
State/Province
Zurich
ZIP/Postal Code
8802
Country
Switzerland
Facility Name
Department of Clinical Psychology and Psychotherapy
City
Bern
ZIP/Postal Code
3014
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
34874888
Citation
van Genugten CR, Schuurmans J, Hoogendoorn AW, Araya R, Andersson G, Banos R, Botella C, Cerga Pashoja A, Cieslak R, Ebert DD, Garcia-Palacios A, Hazo JB, Herrero R, Holtzmann J, Kemmeren L, Kleiboer A, Krieger T, Smoktunowicz E, Titzler I, Topooco N, Urech A, Smit JH, Riper H. Examining the Theoretical Framework of Behavioral Activation for Major Depressive Disorder: Smartphone-Based Ecological Momentary Assessment Study. JMIR Ment Health. 2021 Dec 6;8(12):e32007. doi: 10.2196/32007.
Results Reference
derived
PubMed Identifier
27488181
Citation
Kleiboer A, Smit J, Bosmans J, Ruwaard J, Andersson G, Topooco N, Berger T, Krieger T, Botella C, Banos R, Chevreul K, Araya R, Cerga-Pashoja A, Cieslak R, Rogala A, Vis C, Draisma S, van Schaik A, Kemmeren L, Ebert D, Berking M, Funk B, Cuijpers P, Riper H. European COMPARative Effectiveness research on blended Depression treatment versus treatment-as-usual (E-COMPARED): study protocol for a randomized controlled, non-inferiority trial in eight European countries. Trials. 2016 Aug 3;17(1):387. doi: 10.1186/s13063-016-1511-1.
Results Reference
derived

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E-Compared-CH: Comparative Effectiveness Research on Internet-based Depression Treatment - Swiss Trial

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