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

Physical trauma patients with symptoms of an acute stress disorder: an observational study - The course of acute stress disorder in physical trauma patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43971
Enrollment
300
Registered
2015-12-04
Start date
2016-03-10
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Stress Disorder

Interventions

None listed

Sponsors

Sint Elisabeth Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

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).

Design outcomes

Primary

MeasureTime frame
The first outcome measures are incidence of ASD and PTSD, and anxiety at one year after treatment for physical trauma.

Secondary

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

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)