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Mindful Attention Workshop for Mental Illness (HAZMAT Trial)
N/A
Waitlist Available
Research Sponsored by University of Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up administered at each of the following timepoints: baseline, 1-week follow-up, 2-week follow-up, 1-month follow-up, 3-month follow-up, and 6-month follow-up
Awards & highlights
HAZMAT Trial Summary
This trial is designed to study the effects of Mindful Attention Training (MAT), a mindfulness-based intervention specifically for firefighters, on the health of firefighters. The study will also aim to improve the mental healthcare of firefighters by promoting health service psychologists' contributions to this underserved population.
Eligible Conditions
- Trauma
- Mental Illness
- Post-Traumatic Stress Disorder
- Mindfulness
- Firefighter
HAZMAT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ administered at each of the following timepoints: baseline, 1-week follow-up, 2-week follow-up, 1-month follow-up, 3-month follow-up, and 6-month follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~administered at each of the following timepoints: baseline, 1-week follow-up, 2-week follow-up, 1-month follow-up, 3-month follow-up, and 6-month follow-up
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in PTSD symptom severity
Changes in anxiety symptoms
Changes in depressive symptoms
+5 moreSecondary outcome measures
Evaluate group cohesion
Evaluate group dynamics
Evaluate occupational stress
HAZMAT Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Mindful Attention WorkshopExperimental Treatment1 Intervention
50 participants will be randomized to the Mindful Attention Training (MAT) workshop. The 90-minute workshop will be conducted in group, online format.
Group II: Waitlist ControlActive Control1 Intervention
50 participants will be randomized to the waitlist control condition ("as usual" condition).
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Who is running the clinical trial?
University of HoustonLead Sponsor
147 Previous Clinical Trials
47,400 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
Texas
How old are they?
18 - 65
What site did they apply to?
Trauma and Stress Studies Center
What portion of applicants met pre-screening criteria?
Did not meet criteria
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