Randomized Trial of the Impact of Body Scanning and Intensive Behavioral Intervention on Behavioral Change and Health Outcomes
Coronary Disease, Behavior and Behavior Mechanisms, Hypertension
About this trial
This is an interventional prevention trial for Coronary Disease
Eligibility Criteria
Inclusion Criteria:
Men or women aged 35 and over who provide informed consent to participate including the baseline, interim, and follow-up clinic visits, as well as willingness to participate in the on-line intervention (if selected to be in that group) -
Exclusion Criteria:
Known cardiovascular disease, cancer, or any life-threatening or debilitating illness, including psychiatric illnesses, or significant difficulty with the English language that would preclude successful participation in the program
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Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Behavioral Intervention arm
Control Group
A behavioral intervention consisting of a physician body scan consultation with a radiologist which included viewing self imagery followed by an 18 month behavioral intervention which included educational modules covering: Responding to Stress More Effectively Enhancing the effects of Relaxation Nourishing your immune system Energizing your Body Welcoming Others and Strengthening Relationships
No Intervention