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Clinical Trials/NCT05294848
NCT05294848
Completed
Not Applicable

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

Tel Aviv University1 site in 1 country501 target enrollmentJune 30, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PTSD
Sponsor
Tel Aviv University
Enrollment
501
Locations
1
Primary Endpoint
Post-Combat PTSD Symptoms
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
June 30, 2021
End Date
June 21, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yair Bar-Haim

Professor

Tel Aviv University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Post-Combat PTSD Symptoms

Time Frame: Change from baseline Post-Combat PTSD Symptoms at approximately 1.5 years

Score 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 Outcomes

  • Post-Combat General Anxiety(Change from baseline Post-Combat General Anxiety Symptoms at approximately 1.5 years)
  • Post-Combat Depression(Change from baseline Post-Combat Depression Symptoms at approximately 1.5 years)

Study Sites (1)

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