A study for the effect of traumatic pain and intervention on the incidence of early post-traumatic stress disorder

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900024687

Enrollment

Unknown

Registered

2019-07-21

Start date

2019-08-01

Completion date

Unknown

Last updated

2019-09-16

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

Conditions

Post-traumatic stress disorder(PTSD)

Interventions

PTSD group and non-PTSD group:Trauma was treated routinely without additional intervention.

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18 years or older, agreed to join the researcher; 2) clear mind, normal vision, stable condition and vital signs; 3) no other major stress events within one year; 4) those who can effectively complete the questionnaire.

Exclusion criteria

Exclusion criteria: 1) Severe organic brain injury and blurred vision; 2) Severe traumatic history (sexual assault, etc.), mental illness or mental retardation; 3) drug addicts or drug addicts; 4) critically ill or emotional agitation can not cooperate with investigators; 5) withdrawal from the researcher halfway.

Design outcomes

Primary

Measure	Time frame
PCL-5 score;	—

Countries

China

Contacts

Public ContactXu Tie

Affiliated Hospital of Xuzhou Medical University

xutie889@163.com+86 18052268399

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026