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| ID | Type | Description | Link |
|---|---|---|---|
| P30AG064198-06 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Aging (NIA) | NIH |
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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:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Acceptance- and mindfulness-based exposure therapy (AMBET) | Experimental | Remotely delivered psychotherapy combining exposure therapy with mindfulness. |
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| Present-Centered Therapy (PCT) | Active Comparator | Remotely delivered psychotherapy that focuses on increasing adaptive responses to current life stressors and difficulties. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Acceptance and Mindfulness Based Exposure Therapy | Behavioral | Eight sessions of exposure therapy combined with mindfulness delivered via videoconferencing platform. AMBET will consist of 90-minute weekly sessions for 4 weeks, then every other week for 4 more sessions. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in PTSD symptoms over time | Change in symptoms as measured by the Clinician Administered PTSD Scale (CAPS-5) from pre- to post-treatment. The full score range is 0 - 80, where lower scores indicate lower symptom levels of PTSD. | Baseline, At 6 weeks, Post-treatment: Approximately 3 months and 6 months from intake |
| Measure | Description | Time Frame |
|---|---|---|
| Change in depressive symptoms over time | Change in symptoms as measured by the Hamilton Depression Rating Scale (HDRS-24) from pre- to post-treatment. The full score range is 0 - 76, where lower scores indicate lower symptom levels of depression. | Baseline, At 6 weeks, Post-treatment: approximately 3 months and 6 months from intake |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yuval Neria, Ph.D. | Contact | 212-543-6061 | ny126@cumc.columbia.edu | |
| Maja Bergman, Ph.D. | Contact | 212-543-6061 | mb3829@cumc.columbia.edu |
| Name | Affiliation | Role |
|---|---|---|
| Yuval Neria, PhD | Columbia University | Principal Investigator |
| Maja Bergman, PhD | Columbia University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Columbia University Irving Medical Center | Recruiting | New York | New York | 10032 | United States |
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| Present-Centered Therapy | Behavioral | Twelve 60-minute weekly sessions of psychotherapy delivered via videoconferencing platform. |
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| ID | Term |
|---|---|
| D003130 | Combat Disorders |
| D006323 | Heart Arrest |
| ID | Term |
|---|---|
| D040921 | Stress Disorders, Traumatic |
| D000068099 | Trauma and Stressor Related Disorders |
| D001523 | Mental Disorders |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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