Physical trauma patients with symptoms of an acute stress disorder: an observational study

Completed

• Conditions: Acute Stress Disorder; 10002861

• Registration Number: NL-OMON43971
• Lead Sponsor: Sint Elisabeth Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 2018-05-02
• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 300

Inclusion Criteria

Being treated in the shock room, being aged 18 or older

Exclusion Criteria

Severe neurology trauma (i.e. severe traumatic brain injury (TBI)), dementia, age below 18 years, and insufficient knowledge of the Dutch language (verbal and in writing).

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The first outcome measures are incidence of ASD and PTSD, and anxiety at one<br /><br>year after treatment for physical trauma. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary outcome measures are psychological distress, coping, and QOL.<br /><br><br /><br>Other study parameters are personality and trait anxiety, medical history (e.g.<br /><br>previously treated in shock room due to physical trauma), and history of<br /><br>psychological and/or psychiatric disorders. </p><br>