Actively Recruiting
Combining Antidepressants and Attention Bias Modification in Depression
Led by University of Oslo · Updated on 2025-03-28
246
Participants Needed
1
Research Sites
170 weeks
Total Duration
On this page
Sponsors
U
University of Oslo
Lead Sponsor
U
University of Oxford
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background: Major depressive disorder (MDD) is a highly prevalent psychiatric condition associated with significant disability, mortality and economic burden. A large proportion of MDD patients are treated in primary health care (PHC) in the municipalities and represent a challenging group. Attentional Bias Modification (ABM) training in combination with antidepressants (SSRIs) could be an effective treatment. The overall aim of this study is to test the hypothesis that adding an ABM procedure to regular treatment with antidepressants in PHC will result in further improvement of symptoms compared to treatment with antidepressants alone (treatment as usual, TAU) and as compared to an active comparison condition. Methods: A total of 246 patients with a diagnosis of MDD will be included in this study. The study is a three-armed pragmatic randomized controlled trial comparing the efficacy of ABM as add-on to treatment with antidepressants in primary care (ABM condition) compared to standard antidepressant treatment (TAU condition). In a third group participants will complete the same schedule of intermediate assessments as the ABM condition in addition to TAU , but no ABM, thus controlling for the non-training-specific aspects of the ABM condition (SSRI Active comparison group). Discussion: The clinical outcome of this study may help develop easy accessible, low cost treatment of depression in PHC. Moreover, the study aims to broaden our knowledge of optimal treatment for patients with a MDD by providing adjunct treatment to facilitate recovery and long term gain
CONDITIONS
Official Title
Combining Antidepressants and Attention Bias Modification in Depression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of Major Depressive Disorder
- Beck Depression Inventory II score greater than 14
- Age between 18 and 65 years
- Ability to understand and speak a Scandinavian language
- Willingness and ability to give informed consent
You will not qualify if you...
- Current or past neurological illness
- Traumatic brain injury
- Current alcohol and/or substance dependency disorders
- Psychotic disorders
- Bipolar disorder type 1
- Developmental disorders and mental retardation
AI-Screening
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Trial Site Locations
Total: 1 location
1
Jan Ivar Røssberg
Oslo, Nydalen, Norway, Postboks 4959
Actively Recruiting
Research Team
J
Jan I Røssberg, PhD
CONTACT
N
Nils I Landrø, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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