Study of Physical Health for Women With Posttraumatic Stress or Depression
Recruitment status was Recruiting
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Purpose
The purpose of this study is to obtain a better understanding of how stress is related to health risks.
| Condition |
|---|
|
Healthy Stress, Psychological Depression Posttraumatic Stress Disorders |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Cross-Sectional |
| Official Title: | Cardiovascular Risk in Relation to Posttraumatic Stress Disorder in Young Women |
- 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).
| Estimated Enrollment: | 150 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | August 2012 |
| Estimated Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| Posttraumatic Stress |
| Depression |
| Healthy |
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.
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Community sample, psychology clinics
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
Contacts and Locations| Contact: Jeffrey L Kibler, PhD | 954-262-5942 | whs.nsu@gmail.com |
| Contact: Jeffrey L Kibler, PhD | kibler@nova.edu |
| United States, Florida | |
| Center for Psychological Studies, Nova Southeastern University | Recruiting |
| Fort Lauderdale, Florida, United States, 33314-7796 | |
| Principal Investigator: Jeffrey L Kibler, PhD | |
| Sub-Investigator: Steven Gold, PhD | |
| Sub-Investigator: Mindy Ma, PhD | |
| Principal Investigator: | Jeffrey L Kibler, PhD | Nova Southeastern University |
More Information
No publications provided
| Responsible Party: | Jeffrey L. Kibler, PhD, Nova Southeastern University |
| ClinicalTrials.gov Identifier: | NCT01208844 History of Changes |
| Other Study ID Numbers: | CPS06230812Exp., 1R15HL085121-01A2 |
| Study First Received: | August 30, 2010 |
| Last Updated: | July 19, 2011 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Depression Depressive Disorder Stress Disorders, Post-Traumatic Stress Disorders, Traumatic Stress, Psychological |
Behavioral Symptoms Mood Disorders Mental Disorders Anxiety Disorders |
ClinicalTrials.gov processed this record on June 18, 2013