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Effectiveness of Internet-based Depression Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01636752
Acronym
EVIDENT
Enrollment
1013
Registered
2012-07-10
Start date
2012-07-31
Completion date
2017-02-28
Last updated
2018-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild to Moderate Depressive Symptoms

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).

Interventions

BEHAVIORALDeprexis

Online self-help with and without e-mail-support

Sponsors

University of Luebeck
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* PHQ\>4 and \<15

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Personal Health Questionnaire (PHQ-9)12 wks

Secondary

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

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026