Study of Physical Health for Women With Posttraumatic Stress or Depression

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

59 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-06-30

Study Completion Date

2012-08-31

Brief Summary

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

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Detailed Description

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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.

Conditions

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Healthy Stress, Psychological Depression Posttraumatic Stress Disorders

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Posttraumatic Stress

No interventions assigned to this group

Depression

No interventions assigned to this group

Healthy

No interventions assigned to this group

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes