Multifaceted Intervention to Restore Resilience and Overcome Risk
Launched by ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · May 16, 2025
Trial Information
Current as of July 23, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The MIRROR study is a clinical trial designed to help female veterans who have experienced military sexual trauma (MST) or intimate partner violence (IPV). The trial will compare two different programs aimed at improving how these women manage their emotions and reduce symptoms of post-traumatic stress disorder (PTSD), especially when they also have a history of brain injury. This study is not yet recruiting participants but will focus on women aged 18 and older who can speak English and have experienced MST or IPV, have a history of brain injury, and show some symptoms of PTSD.
To be eligible for this study, participants must be willing to consent and meet certain criteria, such as having experienced IPV or MST and reporting difficulties in managing their emotions. However, those at high risk for suicide or with severe mental health issues will not be able to participate. Women who qualify for this study can expect to engage in activities that aim to enhance their emotional well-being and potentially improve their PTSD symptoms in a supportive environment. This trial is a valuable opportunity for eligible veterans to receive help and support for their experiences.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Able to consent as determined by UBACC, are English-speaking FVets who are 18+ years old
- • Screen positive for exposure to IPV and/or MST using the VA Intimate Partner Violence Assistance Program (VA IPVAP) and MST Screening Protocol,
- • Have a history of at least one BI assessed using the BISQ+IPV,
- • Sub-threshold PTSD (operationalized as a total score of \>33 on the PTSD Checklist Diagnostic and Statistical Manual of Mental Disorders-5 (PCL-5),
- • Report deficits in Emotion Regulation (operationalized as a score of 0.5 SD above published means on the DERS).
- Exclusion Criteria:
- • FVets at high risk for suicide (respond yes to items 3, 4, 5, or 8 on the Columbia Suicide Severity Rating Scale \[C-SSRS\]),
- • Observable active psychosis (e.g., auditory hallucinations, grandiose delusions),
- • Those determined to have problematic substance use (score \> 27 on the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) will be referred to substance use dependence programs for concurrent treatment. The PI and Co-Is will collaborate with the substance use dependence program to determine continued participation.
About Icahn School Of Medicine At Mount Sinai
The Icahn School of Medicine at Mount Sinai is a premier academic institution located in New York City, renowned for its commitment to advancing medical research, education, and patient care. As a leading sponsor of clinical trials, the institution leverages its state-of-the-art facilities and multidisciplinary expertise to drive innovative research initiatives aimed at improving health outcomes. With a focus on translational medicine, the Icahn School of Medicine collaborates with a diverse network of researchers, clinicians, and industry partners to explore novel therapies and interventions across a wide range of medical disciplines. Its rigorous scientific approach and dedication to ethical standards position it as a trusted leader in the clinical research landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Maria Kajankova, PhD
Principal Investigator
Icahn School of Medicine at Mount Sinai
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported