Study of Physical Health for Women With Posttraumatic Stress or Depression

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2010 by Nova Southeastern University.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Information provided by:
Nova Southeastern University
ClinicalTrials.gov Identifier:
NCT01208844
First received: August 30, 2010
Last updated: July 19, 2011
Last verified: August 2010

August 30, 2010
July 19, 2011
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
Not Provided
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
Not Provided
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Non-Probability Sample

Community sample, psychology clinics

  • Healthy
  • Stress, Psychological
  • Depression
  • Posttraumatic Stress Disorders
Not Provided
  • Posttraumatic Stress
  • Depression
  • Healthy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
150
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: Jeffrey L Kibler, PhD 954-262-5942 whs.nsu@gmail.com
Contact: Jeffrey L Kibler, PhD kibler@nova.edu
United States
 
NCT01208844
CPS06230812Exp., 1R15HL085121-01A2
No
Jeffrey L. Kibler, PhD, 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
August 2010

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