Wearable Device-Based Analysis of the Relationship Between Sleep Patterns and Clinical Prognosis in Patients With Traumatic Brain Injury

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorGeneral Hospital of Ningxia Medical University

About this trial

In patients with traumatic brain injury, post-traumatic sleep patterns have the potential to impact clinical prognosis. While some progress has been made in the study of sleep and prognosis in patients with traumatic brain injury, there is still lack of research on the relationship between sleep and clinical prognosis in post-traumatic patients due to differences in study design, patient age, severity of trauma, and definitions of sleep disorders. Additionally, the primary data collection methods employed in most studies have been self-reported sleep assessments, which are subject to potential biases and inaccuracies. Therefore, explore the impact of sleep patterns on clinical prognosis in post-traumatic patients, with potential to advance our comprehension of recovery outcomes in this patient group.

Eligibility criteria

Qualifiers

18~60 years old.

The patient had no sleep disturbance problems prior to traumatic brain injury.

The patient has a definite diagnosis of traumatic brain injury and the Glasgow score is >8.

The patient had abnormal imaging scans.

Disqualifiers

Patients with a previous history of traumatic brain injury, mental illness, alcohol abuse or sleep disorders.

Patients admitted for surgical intervention.

Patients with a combination of other heavy visceral injuries.

Women during pregnancy and lactation.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed