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Cohort Study of Post-Traumatic Stress Disorder (PTSD) in Critically Ill Patients

Cohort Study of Post-Traumatic Stress Disorder (PTSD) in Critically Ill Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123311
Enrollment
Unknown
Registered
2026-04-23
Start date
2026-04-23
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Post-Traumatic Stress Disorder

Interventions

Post-traumatic Stress Disorder Observation Group:None

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. >= 18 years old; 2. ICU hospitalization duration >= 72 hours; 3. The patient or the family member has signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. The condition is extremely critical and the patient may die at any moment; 2. Patients with serious neurological disorders (such as severe brain injury); 3. Those who cannot complete the follow-up, including patients who cannot complete the scales or questionnaires.

Design outcomes

Primary

MeasureTime frame
Psychological Assessment Scales;

Secondary

MeasureTime frame
Quality of Life Scale;

Countries

China

Contacts

Public ContactLi Jinxiu;Xiang Bingjie;Zhang Yan

The Second Xiangya Hospital of Central South University

421511461@qq.com+86 731 85295870

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026