Development of Attention Bias Modification for Depression

NCT ID: NCT02880215

Last Updated: 2019-10-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

145 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-01

Study Completion Date

2019-09-26

Brief Summary

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Although negatively biased attention has a central theoretical and empirical role in the maintenance of depression, there are few behavioral treatments that successfully target and improve this deficit. The current proposal builds upon prior work and aims to further develop an attention bias modification intervention. The investigators propose to develop a highly specific intervention that directly targets negative attention bias and the neurobiology that supports it, using cutting-edge cognitive neuroscience to inform treatment development and improve quality of life of patients whose psychopathology is maintained by negative attention bias.

Detailed Description

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The overall goal of this project is to continue development of an attention bias modification (ABM) intervention that targets and reduces negative attention bias among adults with elevated symptoms of depression. The investigators' prior work indicates that attention bias for negative information is associated with the maintenance of depression and that neural circuitry within frontal-parietal brain networks supports biased attention for negative information, thus allowing us to develop specific and targeted interventions that directly alter the neurobiology of negative attention bias. The proposed R33 study builds upon the investigators' prior National Institute of Mental Health (NIMH) funded work (R21MH092430), which examined whether ABM reduces negative attention bias and improves symptoms of depression. Findings indicate that compared to placebo ABM, active ABM reduced negative attention bias and increased resting state connectivity within a neural circuit (i.e., middle frontal gyrus and dorsal anterior cingulate cortex) that supports control over emotional information. Further, change in negative attention bias from pre- to post-ABM was significantly correlated with depression symptom change but only in the active training condition. Importantly, a 40% decrease in symptoms was observed in the active training condition; however, similar symptom reduction was also observed in the "placebo ABM" condition. Exploratory analyses indicated that placebo training may have promoted depression improvement by enhancing sustained attention. Although these preliminary findings are encouraging and demonstrate that ABM successfully alters the treatment target (i.e., negative attention bias), the investigators' prior work is among the first to document efficacy of ABM among adults with clinically significant depression. It is now prudent and necessary to obtain additional efficacy evidence for ABM before moving forward with large-scale clinical trials of ABM for depression. Aim 1 is to conduct a randomized clinical trial among adults with elevated symptoms of depression and a negative attention bias that compares the efficacy of active ABM to cognitive control training and an assessment-only control condition that does not involve any ABM procedures. Aim 2 is to examine whether ABM alters negative attention bias and functional connectivity within frontal-parietal neural circuitry that support negative attention bias. Aim 3 is to identify mechanisms responsible for the putative efficacy of active ABM and cognitive control training. Study Impact: The current project proposes to target and reduce negative attention bias with a novel intervention grounded in basic psychopathology research. The investigators believe this experimental medicine approach will lead to the development of a highly specific and targeted intervention, using cutting-edge cognitive neuroscience to inform treatment development, and improve the quality of life of people whose psychopathology is maintained by negative attention bias.

Conditions

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Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Attention Bias Modification

Behavioral intervention designed to improved negative attention bias.

Group Type EXPERIMENTAL

Attention Bias Modification

Intervention Type BEHAVIORAL

Behavioral intervention designed to decrease negative attention bias.

Cognitive Control Training

Behavioral intervention designed to improve sustained attention.

Group Type EXPERIMENTAL

Cognitive Control Training

Intervention Type BEHAVIORAL

Behavioral intervention designed to improve sustained attention.

Assessment Only

Assessment only with no active intervention.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Attention Bias Modification

Behavioral intervention designed to decrease negative attention bias.

Intervention Type BEHAVIORAL

Cognitive Control Training

Behavioral intervention designed to improve sustained attention.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* able and willing to provide informed consent;
* fluent in English;
* moderate or greater depression symptoms;
* attention bias for negative stimuli;
* stable psychiatric and neurological medication usage.

Exclusion Criteria

* meets criteria for current substance use disorder (mild or greater severity), current or past psychotic disorder, bipolar disorder, or schizophrenia;
* has any medical or physical conditions that would preclude participation in an fMRI study (e.g., orthodontic braces);
* is currently receiving psychotherapy or electroconvulsive therapy (ECT);
* current opioid analgesics or systemic corticosteroid use for an acute medical condition or taken as needed;
* has had suicidal behaviors or significant suicidal ideation within the last six months.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

University of Texas at Austin

OTHER

Sponsor Role lead

Responsible Party

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Christopher G. Beevers

Professor and Director of the Institute for Mental Health Research

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Mood Disorders Laboratory

Austin, Texas, United States

Site Status

Countries

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United States

References

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Beevers CG, Clasen PC, Enock PM, Schnyer DM. Attention bias modification for major depressive disorder: Effects on attention bias, resting state connectivity, and symptom change. J Abnorm Psychol. 2015 Aug;124(3):463-75. doi: 10.1037/abn0000049.

Reference Type RESULT
PMID: 25894440 (View on PubMed)

Beevers CG, Hsu KJ, Schnyer DM, Smits JAJ, Shumake J. Change in negative attention bias mediates the association between attention bias modification training and depression symptom improvement. J Consult Clin Psychol. 2021 Oct;89(10):816-829. doi: 10.1037/ccp0000683.

Reference Type DERIVED
PMID: 34807657 (View on PubMed)

Other Identifiers

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R33MH109600-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

201600258

Identifier Type: -

Identifier Source: org_study_id

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