- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06710145
The Effect of Using the Combat Attention App on the Risk of Post-traumatic Symptoms
April 8, 2025 updated by: Yair Bar-Haim, Tel Aviv University
Military service and reserve duty in combat units entails exposure to traumatic events that require mental adjustment.
In light of the results of controlled studies that proved the effectiveness an response-time based mechanized training protocol in reducing risk for post-trauma symptoms in deployed combat soldiers, the Israeli Defense Forces decided at the beginning of the Iron Swords War to implement an internet-based App of the intervention.
Soldiers and combat reservists were invited to use the Combat Attention App.
The purpose of this study is to examine the effectiveness of the Combat Attention App in relation to a control group of soldiers who did not use the App in reducing risk for post-traumatic stress symptoms of deployed soldiers.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Participants who used the Combat Attention App before combat deployment and a group of matched (age and sex) participants who did not use the App will be compared on PTSD, depression, and anxiety symptoms post deployment.
Study Type
Observational
Enrollment (Estimated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yair Bar-Haim, PhD
- Phone Number: +972-3-6405465
- Email: yair1@tauex.tau.ac.il
Study Contact Backup
- Name: Chelsea Gober Dykan, MA
- Phone Number: +972-3-6405465
- Email: chelseagober@mail.tau.ac.il
Study Locations
-
-
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Tel Aviv, Israel
- Tel Aviv University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population consists of enlisted and reservist soldiers who participated in the Iron Swards war and either used or did not use the attention App.
Description
Inclusion criteria:
- Age over 18 years.
- Served as an enlisted soldier or reservist during the Iron Swards War.
- Used the Combat Attention App or can serve as a matched control who did not use the App.
- Colloquial Hebrew sufficient to fill out the research questionnaires.
Exclusion criteria:
- Below 18 years of age.
- Colloquial Hebrew that is insufficient to fill out the research questionnaires.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Attention App Users
Soldiers who used the App and completed at least one training session
|
The Combat Attention App is a response-time based mechanized preventive intervention designed to train combat soldiers' attention toward threats before combat exposure in order to reduce the risk for combat-related post-trauma symptoms.
In light of the results of controlled studies that proved the efficacy of this preventive intervention, the Israel Defense Forces (IDF) decided at the beginning of the Iron Swords War (October 7th, 2023) to implement an internet-based App of the intervention, and soldiers and combat reservists were invited to train on the Combat Attention App.
|
|
Non Users
Soldiers matched on age, sex, and specialty to the Attention App Users group who never used the App
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PTSD Checklist for DSM-5 (PCL-5)
Time Frame: January-June 2025
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Measures PTSD symptoms according to DSM-5
|
January-June 2025
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IDF Medical Records
Time Frame: January-June 2025
|
Holds all the medical information and contact with health/mental health professionals during one's service
|
January-June 2025
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Combat Experiences Scale
Time Frame: January-June 2025
|
Measures the occurrence of specific combat events
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January-June 2025
|
|
Patient Health Questionnaire 9 (PHQ-9)
Time Frame: January-June 2025
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Measures Depression symptoms according to DSM-5
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January-June 2025
|
|
Attention Bias Questionnaire (ABQ)
Time Frame: January-June 2025
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Measures subjective experiences of attention allocation to threats
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January-June 2025
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GAD-7
Time Frame: January-June 2025
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measures symptoms of generalized anxiety disorder
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January-June 2025
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Dissociative Experiences Scale (DES)
Time Frame: January-June 2025
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measures dissociative symptoms associated with trauma exposure
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January-June 2025
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yair Bar-Haim, PhD, Tel Aviv University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 1, 2026
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
October 31, 2024
First Submitted That Met QC Criteria
November 25, 2024
First Posted (Actual)
November 29, 2024
Study Record Updates
Last Update Posted (Actual)
April 11, 2025
Last Update Submitted That Met QC Criteria
April 8, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TAU-Combat-Attention
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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