Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT05503966

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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