Evaluating the Alliance180 Program's effects on well-being

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.