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Clinical Trials/NCT01208844
NCT01208844
Completed
Not Applicable

Cardiovascular Risk in Relation to Posttraumatic Stress Disorder in Young Women

Nova Southeastern University1 site in 1 country59 target enrollmentJune 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Nova Southeastern University
Enrollment
59
Locations
1
Primary Endpoint
Number of Cardiovascular Risk Factors
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to obtain a better understanding of how stress is related to health risks.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
August 2012
Last Updated
11 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jeffrey Kibler, Ph.D.

Professor

Nova Southeastern University

Eligibility 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

Outcomes

Primary Outcomes

Number of Cardiovascular Risk Factors

Time Frame: Single assessment timepoint

This primary outcome will be assessed at the second study visit (1-7 days from first study visit for those who are eligible).

Study Sites (1)

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