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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01661452
Other study ID # F110510007
Secondary ID
Status Completed
Phase N/A
First received August 7, 2012
Last updated December 2, 2013
Start date June 2011
Est. completion date September 2013

Study information

Verified date November 2013
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

A survey (patient self-report) of patients presenting to UAB emergency room, outpatient trauma clinics and substance abuse center for symptoms of post-traumatic stress disorder and maladaptive coping responses after the widespread tornado disaster that occurred in Alabama in April 2011.


Recruitment information / eligibility

Status Completed
Enrollment 629
Est. completion date September 2013
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

- 19 and older Able and willing to complete a questionnaire

Exclusion Criteria:

- Younger than 19 Unwilling or unable to complete a questionnaire

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
Referral to counseling services if desired


Locations

Country Name City State
United States University of Alabama Birmingham Birmingham Alabama

Sponsors (1)

Lead Sponsor Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Development of PTSD June 2011-December 2012 No