Trial of Acceptance and Mindfulness-based Exposure Therapy (AMBET) and Present Centered Therapy (PCT) (NCT07410481)
A Randomized Clinical Trial of Acceptance and Mindfulness-based Exposure Therapy (AMBET) and Present Centered Therapy (PCT)
๐ฉบ Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to learn if a new therapy called Acceptance- and Mindfulness-Based Exposure Therapy (AMBET) helps treat post-traumatic stress disorder (PTSD) in people who survived a cardiac arrest. This study will compare AMBET to another psychotherapy treatment called Present Centered Therapy (PCT) to see which therapy is more effective in treating PTSD. The main questions it aims to answer are: Does AMBET reduce PTSD symptoms in survivors of cardiac arrest? How do the benefits of AMBET compare to PCT? Participants will: * Be randomly assigned to receive either AMBET or PCT * Attend 12 hours of individual psychotherapy sessions over about 12 weeks * Complete short weekly surveys about their mood and behaviors online * Wear a Fitbit device to track sleep and activity during the study * Do brief homework assignments between sessions
Who can join: Review the eligibility criteria below.
Location: Columbia University Irving Medical Center โ New York, New York
Age range: 18 Years to 81 Years
๐งช Interventions in This Study
- Acceptance and Mindfulness Based Exposure Therapy (BEHAVIORAL)
- Present-Centered Therapy (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Columbia University Irving Medical Center โ New York, New York
๐ Contact the Study Coordinator
Phone: (212) 543-6061
Email: ny126@cumc.columbia.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in PTSD - Post Traumatic Stress Disorder
- Trifecta Research Study โ Northridge, California
- Diet and Microbiome Interactions: Application in Posttraumatic Stress Disorder in Adults Consuming Vegetable Drinks โ Fort Collins, Colorado
- ONE-P TMS First Responders โ Vancouver, British Columbia
- Suvorexant 3 - PE-PC โ San Francisco, California
- Initial Study Sesting Efficacy and Tolerability of PT150 for PTSD in Veterans โ San Diego, California
- Adaptation of the STAIR-NT for First Responders โ Forest Lake, Minnesota
Explore by condition: All PTSD - Post Traumatic Stress Disorder clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.