Analysis of Influencing Factors for the Development of PTSD in Emergency Department Trauma Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorThe First Affiliated Hospital of Air Force Medicial University

About this trial

The goal of this observational study is to learn about the long-term effects of key factors such as cognitive flexibility, social support, and physiological stress on the occurrence of Post-Traumatic Stress Disorder (PTSD) in adult trauma patients treated in the emergency department. The main question it aims to answer is:

Among emergency department patients who have experienced major trauma, can factors such as early post-trauma cognitive flexibility, level of social support, inflammatory markers, and trauma severity predict the development of PTSD within 6 months? Participants will complete a series of online questionnaires and clinical assessments at baseline, 1 month, 3 months, and 6 months after the traumatic event.

Eligibility criteria

Qualifiers

Age between 18 and 65 years old (inclusive);

Experienced a life-threatening major traumatic event, clearly diagnosed by a clinician;

The patient is able to communicate normally with medical staff through language;

The subject is fully informed and voluntarily signs the informed consent form.

Disqualifiers

History of psychiatric disorders or current use of psychotropic medications;

Pre-existing cognitive impairment (e.g., dementia, Alzheimer's disease);

Terminal illnesses (such as advanced malignant tumors, end-stage organ failure, advanced neurological diseases, or any other condition judged by the attending physician to have a life expectancy of less than 6 months);

Inability to cooperate with follow-up.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations