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Stress Management Program for Heart Attack
N/A
Waitlist Available
Research Sponsored by University of California, Davis
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 about 10 weeks
Awards & highlights
Study Summary
This trial will use PET/CT scans to study how stress affects the inflammation of arteries and the activation of the amygdala.
Eligible Conditions
- Heart Attack
- Cardiovascular Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ about 10 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~about 10 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in amygdala activation
Trial Design
1Treatment groups
Experimental Treatment
Group I: SMART ProgramExperimental Treatment1 Intervention
The Stress Management and Resiliency Training (SMART) Program is a multimodal mind-body and cognitive skills-based program that teaches participants a variety of different approaches for reducing their physiologic stress response. The program is delivered virtually (online) for 1.5 hours once a week for 8 weeks.
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Who is running the clinical trial?
University of California, DavisLead Sponsor
914 Previous Clinical Trials
4,720,828 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- If your stress level is 14 or higher on a certain test you take before the study, you cannot participate.You meditate for at least 10 minutes every day.You have a physical or mental health condition that makes it hard to take part in the study or have a PET scan.You are currently taking part in a study for people who have recently had a heart attack.
Research Study Groups:
This trial has the following groups:- Group 1: SMART Program
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there vacancies available for participants in this clinical trial?
"The clinical trial is currently looking for participants, having been posted on the 11th of May 2022 and recently modified on 8th June."
Answered by AI
How many participants are being recruited for this research initiative?
"Affirmative. The clinical trial post on clinicaltrials.gov declares that this experiment is actively recruiting patients; it was posted on May 11th 2022 and last edited June 8th 2022. At the moment, 10 participants are needed at one medical centre for participation in the study."
Answered by AI
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