Cortisol Diurnal Variation and the Risk for Developing Post Traumatic Stress Disorder

NCT01914861 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2013-08-02

No results posted yet for this study

Summary

The purpose of this study is to examine a possible link between the time of day of exposure to a traumatic event and the risk of developing post-traumatic stress disorder. Clinical and biological correlates will also be examined from this perspective.

Conditions

  • Posttraumatic Stress Disorders
  • Cortisol Diurnal Variation

Sponsors & Collaborators

  • Sheba Medical Center

    lead OTHER_GOV

Eligibility

Min Age
21 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2013-12-31

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01914861 on ClinicalTrials.gov