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Combining Antidepressants and Attention Bias Modification in Depression - Trial NCT05503966

Access comprehensive clinical trial information for NCT05503966 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Oslo and is currently Recruiting. The study focuses on Depressive Disorder. Target enrollment is 246 participants.

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NCT05503966
Recruiting
behavioral
Trial Details
ClinicalTrials.gov โ€ข NCT05503966
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Combining Antidepressants and Attention Bias Modification in Depression
Combining Antidepressants and Attention Bias Modification in Depression: A Randomized Controlled Trial in Primary Care

Study Focus

Depressive Disorder

Attentional Bias Modification

Interventional

behavioral

Sponsor & Location

University of Oslo

Oslo, Norway

Timeline & Enrollment

N/A

Sep 22, 2022

Dec 30, 2024

246 participants

Primary Outcome

Hamilton Depression Rating Scale,Beck Depression Inventory II

Summary

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

ICD-10 Classifications

Depressive conduct disorder
Recurrent depressive disorder, unspecified
Recurrent depressive disorder
Other recurrent depressive disorders
Recurrent depressive disorder, currently in remission

Data Source

ClinicalTrials.gov

NCT05503966

Non-Device Trial