Evaluating the Alliance180 Program's effects on well-being
Effects of "Alliance180 Program" on Psychological and Physical Well-Being
This study is testing if the Alliance180 Program can improve the physical and mental well-being of US Veterans, First Responders, and Front Line Healthcare Workers.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | All |
| Sponsor | University of North Carolina, Chapel Hill Academic / other |
| Locations | 2 sites (Saratoga Springs, New York and 1 other locations) |
| Trial ID | NCT06451523 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to assess the impact of the Alliance180 Program on the physical and psychological well-being of adults who are or were US Veterans, First Responders, and Front Line Healthcare Workers. Participants will complete self-report measures related to feelings of safety, autonomic functioning, and mental health indices before and after the program. The study will track changes in these measures at multiple time points: one week, one month, three months, and six months post-intervention. Data collection will be conducted remotely using the REDCap system from the University of North Carolina, Chapel Hill.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are current or former US Veterans, First Responders, or Front Line Healthcare Workers experiencing trauma-related symptoms.
Not a fit: Patients who have previously completed the Alliance180 Program will not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve the mental health and overall well-being of individuals exposed to trauma.
How similar studies have performed: Other studies have shown promising results with similar therapeutic approaches, particularly in trauma and stress-related interventions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years or older * Enrollment in an upcoming "Alliance180 Program". (Enrollment is limited to adults who currently or formerly serve as US Veterans, First Responders and/or Front Line Healthcare Workers and are currently experiencing symptoms related to trauma exposure) Exclusion Criteria: \- Individuals who have previously completed the "Alliance180 Program"
Where this trial is running
Saratoga Springs, New York and 1 other locations
- Alliance180 — Saratoga Springs, New York, United States (Recruiting)
- University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Keri J Heilman, PhD — University of North Carolina, Chapel Hill
- Study coordinator: Keri J Heilman, PhD
- Email: keri_heilman@med.unc.edu
- Phone: 913-802-2168
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.