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View Clinical Trial (Medical Research Study)


Cardiovascular Risk in Relation to Posttraumatic Stress Disorder in Young Women

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City:   Fort Lauderdale
State:   Florida
Zip Code:   33314
Conditions:   Healthy - Stress, Psychological - Depression - Posttraumatic Stress Disorders
Purpose:   The purpose of this study is to obtain a better understanding of how stress is related to health risks.
Study Summary:   Participants complete up to two study visits of approximately 3-4 hours each. The first study visit involves an interview about life experiences and emotions. If the participant is eligible for the second assessment, the average length of time between visit 1 and visit 2 will be 1-7 days. The second visit included physical measurements such as cholesterol and blood pressure, performing math and speaking tasks, and surveys to help us learn about healthy behaviors and emotions. No further follow-up of participants is conducted beyond the two study visits.
Criteria:   Inclusion Criteria: - Pre-menopausal - Must be able to speak and read English fluently Exclusion Criteria: - Specific medications and chronic diseases - History of heart attack (myocardial infarction) - Pregnant or given birth in last 3 months - Peri-menopausal or post-menopausal
NCT ID:   NCT01208844
Primary Contact:   Principal Investigator
Jeffrey L Kibler, PhD
Nova Southeastern University

Jeffrey L Kibler, PhD
Phone: 954-262-5942
Email: whs.nsu@gmail.com
Backup Contact:   Email: kibler@nova.edu
Jeffrey L Kibler, PhD
Location Contact:   Fort Lauderdale, Florida 33314
United States



There is no listed contact information for this specific location.

Site Status: Recruiting

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  • Clinical trials for Depression in Fort Lauderdale, Florida

Data Source:   ClinicalTrials.gov
Date Processed:   June 18, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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