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| Sponsored by: |
National Institute of Mental Health (NIMH) |
| Information provided by: | National Institute of Mental Health (NIMH) |
| ClinicalTrials.gov Identifier: | NCT00364910 |
Purpose
This study will evaluate the safety and efficacy of cognitive behavioral therapy in treating people who are experiencing post-traumatic stress disorder (PTSD) after a heart attack.
| Condition | Intervention | Phase |
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Stress Disorders, Post-Traumatic |
Behavioral: Cognitive behavioral therapy (CBT) Behavioral: Educational session and treatment as usual |
Phase I Phase II |
| MedlinePlus related topics: | Depression Heart Attack Mental Health Post-Traumatic Stress Disorder Stress |
| ChemIDplus related topics: | Attapulgite Bismuth subsalicylate Kaopectate |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | PTSD Treatment in Cardiac Patients |
| Estimated Enrollment: | 60 |
| Study Start Date: | April 2006 |
| Estimated Study Completion Date: | April 2008 |
| Estimated Primary Completion Date: | April 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|
A: Experimental
Participants will receive cognitive behavioral therapy
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Behavioral: Cognitive behavioral therapy (CBT)
Participants meet with a therapist for three to five sessions brief exposure-based CBT.
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B: Active Comparator
Participants will receive an educational session and treatment as usual
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Behavioral: Educational session and treatment as usual
Participants assigned to the educational session attend one meeting with a researcher to discuss the results from their evaluation. They could also be referred to a mental health clinic of their choice to help relieve their symptoms.
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PTSD usually develops in people who have experienced a traumatic or life-threatening event, including a health scare like a heart attack or catheterization. Symptoms of PTSD typically include anxiety, anger, and flashbacks or nightmares. PTSD symptoms are also associated with poor medical outcomes and nonadherence to medication after a heart attack. Fortunately, PTSD can sometimes be treated by antidepressants, anti-anxiety medication, and talk therapy. This study will compare the efficacy of cognitive-behavioral therapy (CBT) versus education and treatment as usual for treating people who are experiencing PTSD that is related to their cardiovascular illness (a heart attack or an invasive procedure such as catheterization).
Participants in this single-blind study will receive a psychiatric evaluation during which post-traumatic symptoms and feelings regarding their cardiovascular illness will be evaluated. Participants will then be randomly assigned to receive either CBT or a single educational session about PTSD, with up to 2 more follow-up educational meetings if needed. Participants assigned to the educational session will attend one meeting with a researcher to discuss the results from their evaluation. If they choose, they will also be referred to a mental health clinic for further care. Participants assigned to receive CBT will meet with a therapist once a week for at least 3 weeks. Participants will be offered the chance to meet with their therapist for two additional sessions if they need more time to discuss their symptoms. All participants will be re-evaluated at Months 2 and 6 using an interview, questionnaires,blood tests, blood pressure readings, and weight measurements.
Eligibility
| Ages Eligible for Study: | 21 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Rachel Annunziato, PhD | 212-659-9143 | rachel.annunziato@mssm.edu |
| United States, New York | |||||
| Elmhurst Hospital Center | Recruiting | ||||
| Queens, New York, United States | |||||
| Mount Sinai School of Medicine | Recruiting | ||||
| New York, New York, United States, 10029 | |||||
| Principal Investigator: | Eyal Shemesh, MD | Mount Sinai School of Medicine |
More Information
| Responsible Party: | Children's Hospital of Philadelphia / Mount Sinai Medical Center ( Eyal Shemesh, MD ) |
| Study ID Numbers: | MH071249, 03-0985 DAHBR 96-BHC |
| First Received: | August 15, 2006 |
| Last Updated: | February 29, 2008 |
| ClinicalTrials.gov Identifier: | NCT00364910 |
| Health Authority: | United States: Federal Government |
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