Stress Inoculation Training for Stress
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It might be best to discuss this with the study team or your doctor.
What data supports the effectiveness of the treatment DCA-FF, SIT for stress?
Research shows that Stress Inoculation Training (SIT) is effective in reducing anxiety and stress symptoms, improving performance under stress, and decreasing the need for psychiatric readmissions. It has been successfully used in military settings and with psychiatric inpatients, suggesting its potential effectiveness for stress management.12345
How is Stress Inoculation Training (SIT) different from other treatments for stress?
Stress Inoculation Training (SIT) is unique because it is a cognitive-behavioral treatment that focuses on preparing individuals to handle stress by exposing them to stressors in a controlled environment, helping them develop coping strategies. Unlike other treatments that may focus on reducing stress symptoms after they occur, SIT aims to build resilience and improve performance under stress by training individuals before they encounter real-life stressors.13456
What is the purpose of this trial?
The purpose of this study is to demonstrate the feasibility of augmenting existing/traditional Navy military training with the manualized SIT Core Protocol (CP) utilizing the established augmentation procedure set as measured by feasibility, utility, and satisfaction metrics (CSQ-8) and to examine the relative effectiveness of the SIT-CP by comparison to standard military training in a controlled trial examining outcomes of stress tolerance, psychological health, resilience and occupational performance in Sailors undergoing DCA Firefighting Training (pre- to post-training), while collecting implementation data.
Research Team
Sarah Jackson, MFT, PhD
Principal Investigator
The University of Texas Health Science Center, Houston
Eligibility Criteria
This trial is for US Navy service members who are fluent in English, can give informed consent, have access to a smartphone or computer, and agree to undergo testing throughout the study. They must be available for the entire study duration but with flexibility for military demands.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Training Augmentation
Participants undergo augmented Navy military training with the SIT Core Protocol
Follow-up
Participants are monitored for stress tolerance, psychological health, resilience, and occupational performance
Treatment Details
Interventions
- DCA-FF
- SIT
Find a Clinic Near You
Who Is Running the Clinical Trial?
The University of Texas Health Science Center, Houston
Lead Sponsor
Department of Defense / Congressionally Mandated Research Program (CDMRP)
Collaborator