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NCT06451523 · ClinicalTrials.gov registry record · NA
Effects of "Alliance180 Program" on Well-Being
A NA study of Trauma and Stressor Related Disorders, sponsored by University of North Carolina, Chapel Hill.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 2
- Study locations
NCT06451523: Recruiting NA study of Trauma and Stressor Related Disorders, sponsored by University of North Carolina, Chapel Hill.
NCT06451523 is a NA study of Trauma and Stressor Related Disorders that is actively recruiting participants, run by University of North Carolina, Chapel Hill. The registered enrollment target is 50 participants, below the 61-participant average among 9 other Trauma and Stressor Related Disorders trials with a reported enrollment target (18% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06451523, a NA study of Trauma and Stressor Related Disorders, is actively recruiting participants, sponsored by University of North Carolina, Chapel Hill.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 2
- Study locations
Study Summary
The goal of this clinical trial is to evaluate the effects of the Alliance180 Program on physical and psychological well-being on adults who are/were US Veterans, First Responders and/or Front Line Healthcare Workers. The study aims are: * Aim #1: to evaluate the effect of the Alliance180 Program on physical and psychological well-being in adults who are/were US Veterans, First Responders and/or Front Line Healthcare Workers; * Aim #2: to evaluate the relationship between between feelings of safety and well-being, autonomic functioning, and mental health indices (depression, anxiety, trauma response) before and after the intervention. Participants will be asked to complete self-report measures of feelings of safety and well-being, autonomic functioning, and mental health indices (depression, anxiety, trauma response) before participating in the Alliance180 Program (i.e., baseline research session) and 1 week, 1 month, 3 months and 6 months after completing the Alliance180 Program. Demographic information will be documented during the baseline research session.
Primary Outcome
The Anxiety Subscale of the Hospital Anxiety and Depression Scale (HADS) is a 7-item self-report questionnaire measuring the frequency of anxiety over the prior week. The anxiety subscale ranges from 0 to 21, with higher scores indicating higher anxiety complaints. Repeated measures ANOVA will be used to evaluate significant differences in change scores using a 0.05 significance level.
Conditions Studied
Interventions
- OTHER Alliance180 Program
Study Locations (2)
New York
- Alliance180 - Saratoga Springs
North Carolina
- University of North Carolina at Chapel Hill - Chapel Hill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-06-24 |
| Est. Completion | 2026-09 |
| Phase | NA |
What NCT06451523 shows while recruiting
NCT06451523 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 61-participant average among 9 other Trauma and Stressor Related Disorders trials with a reported enrollment target (18% lower).
The record links to 1 condition, with Trauma and Stressor Related Disorders appearing as the primary indexed condition, and to 1 intervention - of which Alliance180 Program is the first listed.
NCT06451523 reports a single indexed study location in New York, North Carolina.
Frequently Asked Questions
What is clinical trial NCT06451523 about?
NCT06451523 is a clinical study titled "Effects of "Alliance180 Program" on Well-Being". The goal of this clinical trial is to evaluate the effects of the Alliance180 Program on physical and psychological well-being on adults who are/were US Veterans, First Responders and/or Front Line Healthcare Workers. The study aims are: * Aim #1: to evaluate the effect of the Alliance180 Program ...
What is the current status of trial NCT06451523?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-06-24. Estimated completion is 2026-09.
What conditions does trial NCT06451523 study?
This clinical trial studies the following conditions: Trauma and Stressor Related Disorders.
What interventions are being tested in trial NCT06451523?
The interventions under investigation include: Alliance180 Program (OTHER).
Who is sponsoring clinical trial NCT06451523?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06451523 being conducted?
This trial has 2 study locations across New York, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06451523's enrollment target sits among peer trials
50 4th of 9 higher than 6 of 9 other Trauma and Stressor Related Disorders trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Trauma and Stressor Related Disorders trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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