European Comparative Effectiveness Research on Internet-based Depression Treatment in Poland

NCT02389660 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2018-06-29

No results posted yet for this study

Summary

Effective, accessible, and affordable depression treatment is of high importance considering the large individual and economic burden of depression. There is ample support for the effectiveness of Internet-based Cognitive Behavioral Therapy (CBT) for depression which is considered a promising alternative to routine depression treatment strategies. Most evidence comes from randomized controlled trials, however, and not from research in routine practice.

The European Comparative Effectiveness Research on Internet-based Depression Treatment (E-COMPARED) in Poland aims to compare the clinical and cost-effectiveness of blended CBT for adults with major depressive disorder (MDD) with treatment as usual (TAU). The trial will be conducted in routine mental health care in Poland, and is a part of the bigger project funded by European Commission (Grant Agreement No: 603098). In this randomized controlled trial, a total of 150 patients with MDD will be assigned to one of two conditions: 1) blended CBT, 2) TAU. Respondents in both conditions will be followed until 12 months after baseline (measures will be taken at baseline, 3 months, 6 months and 12 months).

Conditions

Interventions

BEHAVIORAL

Blended Cognitive Behavioural Therapy (CBT)

BEHAVIORAL

Treatment as usual

Sponsors & Collaborators

  • VU University of Amsterdam

    collaborator OTHER
  • Linkoeping University

    collaborator OTHER_GOV
  • University of Erlangen-Nürnberg

    collaborator OTHER
  • London School of Hygiene and Tropical Medicine

    collaborator OTHER
  • GGZ inGeest

    collaborator OTHER
  • Universitat Jaume I

    collaborator OTHER
  • Leuphana Universität Lünenberg

    collaborator UNKNOWN
  • University of Limerick

    collaborator OTHER
  • University of Bern

    collaborator OTHER
  • University of Valencia

    collaborator OTHER
  • Inesc Porto

    collaborator UNKNOWN
  • Institut National de la Santé Et de la Recherche Médicale, France

    collaborator OTHER_GOV
  • European Commission

    collaborator OTHER
  • Ministry of Science and Higher Education, Poland

    collaborator OTHER_GOV
  • University of Social Sciences and Humanities, Warsaw

    lead OTHER

Principal Investigators

  • Roman Cieslak, PhD · University of Social Sciences and Humanities

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2018-06-30
Completion
2018-06-30

Countries

  • Poland

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02389660 on ClinicalTrials.gov