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Clinical Trials/NCT01636752
NCT01636752
Completed
N/A

Effectiveness of Internet-based Depression Treatment

University of Luebeck4 sites in 1 country1,013 target enrollmentJuly 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mild to Moderate Depressive Symptoms
Sponsor
University of Luebeck
Enrollment
1013
Locations
4
Primary Endpoint
Personal Health Questionnaire (PHQ-9)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Care for people suffering from depressive symptoms should be given in a step-wise approach. One first step can be the provision of self-help material. Online self-help is an innovative way of providing self-help. The investigators want to study the effect of an interactive online self-help-program (Deprexis) in the treatment of mild to moderate depressive symptoms. Participants will be randomised to either twelve weeks of online-self help or a waiting-list control. Symptoms of depression and other aspects will be assessed over a one year period. Thereafter the controls will also receive online-self help. The investigators hypothesise that online self-help is superior to the control condition in alleviating depressive symptoms and preventing full blown depression.

Detailed Description

This study is supported by the German Ministry of Health (BMG) and is a collaborative project of Universität Bern (PD Dr. Thomas Berger), Charité Berlin (PD Dr. Matthias Rose), Universität Bielefeld (Prof. Dr. Wolfgang Greiner), Universität Hamburg (Prof. Dr. Steffen Moritz, Prof. Dr. Bernd Löwe), GAIA AG Hamburg (Dr. Björn Meyer), Universität Tübingen (Prof. Dr. Martin Hautzinger) and Universität Trier (Prof. Dr. Wolfgang Lutz).

Registry
clinicaltrials.gov
Start Date
July 2012
End Date
February 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Luebeck
Responsible Party
Principal Investigator
Principal Investigator

Philipp Klein

Coordinating Investigator

University of Luebeck

Eligibility Criteria

Inclusion Criteria

  • PHQ\>4 and \<15

Exclusion Criteria

  • acute suicidality
  • psychotic d/o, bipolar d/o or other severe psychiatric d/o

Outcomes

Primary Outcomes

Personal Health Questionnaire (PHQ-9)

Time Frame: 12 wks

Secondary Outcomes

  • Quick Inventory of Depressive Symptoms (QIDS)(12 wks, 6 mths, 12 mths)
  • Personal Health Questionnaire (PHQ-9)(6 mths, 12 mths)
  • Hamilton Rating Scale for Depression (HRSD)(12 wks, 6 mths, 12 mths)

Study Sites (4)

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