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Increasing Psychological Resilience in Combat Soldiers Applying Advanced Eye-Tracking-Based Attention Bias Modification

Increasing Psychological Resilience in Combat Soldiers Applying Advanced Eye-Tracking-Based Attention Bias Modification

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05294848
Enrollment
501
Registered
2022-03-24
Start date
2021-06-30
Completion date
2024-06-21
Last updated
2025-04-11

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

Conditions

Anxiety Disorders, Depression, PTSD

Keywords

Attention Bias Modification, Eye-tracking, Randomized Control Trial

Brief summary

Military service in combat units entails exposure to traumatic events that require mental adjustment. To develop and efficiently apply attention bias modification interventions aimed at enhancing soldiers' mental resilience, it is essential to test the efficiency of such training programs in RCTs. The purpose of the current study is to examine the efficiency of a new attention eye-tracking-based training protocol, in comparison to an RT-based training protocol, and to a control group, in reducing risk for post-trauma symptoms in combat deployed soldiers.

Detailed description

Following the explanation to participants regarding the study process, those who give written consent to participate will be randomly placed into one of three groups: GCFT (N=180), ABMT (N=180), and a neutral control group - RT-based task (N=180). The study will include 3 measurement points: before attention training (in basic training before deployment), after attention training (in basic training camp, still before deployment), and after a combat deployment cycle (6-12 months - to be determined based on the military deployment mission of the participants). In each measurement point, the participants will complete computerized tasks to measure attention and will complete self-report questionnaires.

Interventions

Feedback according to participants' viewing patterns, in order to modify their attention toward threat stimuli.

BEHAVIORALAttention Bias Modification

Attention training via repeated trials of a dot-probe task intended to direct attention toward threat stimuli using threat and neutral face stimuli.

BEHAVIORALNeutral Control

Dot-probe task using only neutral stimuli with no training toward threat

Sponsors

Tel Aviv University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Intervention model description

Parallel random assignment to 3 arms in 1:1:1 ratio.

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Each soldier from the allocated cohort who gives written consent will be able to participate in the study.

Exclusion criteria

* Hebrew proficiency is insufficient to complete the study questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Post-Combat PTSD SymptomsChange from baseline Post-Combat PTSD Symptoms at approximately 1.5 yearsScore on on self-report questionnaire Posttraumatic stress disorder checklist for DSM-5 (PCL-5). The total score, ranging from 0 to 80, reflects PTSD symptom severity, with higher scores representing greater severity.

Secondary

MeasureTime frameDescription
Post-Combat General AnxietyChange from baseline Post-Combat General Anxiety Symptoms at approximately 1.5 yearsScore on self-report questionnaire Generalized Anxiety Disorder questionnaire (GAD-7). The total score, ranging from 0 to 21, reflects GAD symptom severity, with higher scores representing greater severity.
Post-Combat DepressionChange from baseline Post-Combat Depression Symptoms at approximately 1.5 yearsScore on self-report Patient Health Questionnaire 9 (PHQ-9). The total score, ranging from 0-27, reflects severity of depressive symptoms, with higher scores representing greater severity

Other

MeasureTime frameDescription
Post-Training RT-based Attention Bias toward threatChange from baseline Attention Bias within 6 months of baseline measurementChange in Attention Bias will be assessed with a response-time based dot-probe task.
Post-Training Subjective Attention Bias toward threatChange from baseline Attention Bias within 6 months of baseline measurementChange in Subjective Attention Bias will be assessed with a self-reported attention bias using the Attention Bias Questionnaire (ABQ). The total score, ranging from 0 to 36, represents threat-related attention bias, with higher scores representing greater bias toward threat.
Post-Training Eye-tracking Attention Bias toward threatChange from baseline Attention Bias within 6 months of baseline measurementChange in Attention Bias will also be assessed with an eye-tracking task.

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026