Study of Physical Health for Women With Posttraumatic Stress or Depression

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Jeffrey Kibler, Ph.D., Nova Southeastern University
ClinicalTrials.gov Identifier:
NCT01208844
First received: August 30, 2010
Last updated: April 27, 2015
Last verified: April 2015

August 30, 2010
April 27, 2015
June 2008
August 2012   (final data collection date for primary outcome measure)
Number of Cardiovascular Risk Factors [ Time Frame: Single assessment timepoint ] [ Designated as safety issue: No ]
This primary outcome will be assessed at the second study visit (1-7 days from first study visit for those who are eligible).
Same as current
Complete list of historical versions of study NCT01208844 on ClinicalTrials.gov Archive Site
Not Provided
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Study of Physical Health for Women With Posttraumatic Stress or Depression
Cardiovascular Risk in Relation to Posttraumatic Stress Disorder in Young Women

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

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.

Observational
Observational Model: Case Control
Time Perspective: Cross-Sectional
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Non-Probability Sample

Community sample, psychology clinics

  • Healthy
  • Stress, Psychological
  • Depression
  • Posttraumatic Stress Disorders
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  • Posttraumatic Stress
  • Depression
  • Healthy
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
59
August 2012
August 2012   (final data collection date for primary outcome measure)

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
Female
18 Years to 50 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01208844
CPS06230812Exp., 1R15HL085121-01A2
No
Jeffrey Kibler, Ph.D., Nova Southeastern University
Nova Southeastern University
National Heart, Lung, and Blood Institute (NHLBI)
Principal Investigator: Jeffrey L Kibler, PhD Nova Southeastern University
Nova Southeastern University
April 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP