Analyzing how sleep patterns affect recovery in traumatic brain injury patients
Wearable Device-Based Analysis of the Relationship Between Sleep Patterns and Clinical Prognosis in Patients With Mild to Moderate Traumatic Brain Injury
This study looks at how sleep patterns affect recovery in adults aged 18 to 60 who have had a traumatic brain injury.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | General Hospital of Ningxia Medical University Academic / other |
| Locations | 1 site (Yinchuan, Ningxia) |
| Trial ID | NCT06790979 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the relationship between sleep patterns and clinical prognosis in patients who have experienced traumatic brain injury (TBI). By utilizing wearable devices to collect objective sleep data, the study aims to overcome the limitations of self-reported assessments that are often biased. The research focuses on patients aged 18 to 60 who have a confirmed diagnosis of TBI and meet specific inclusion criteria, with the goal of enhancing understanding of recovery outcomes based on sleep quality. The findings could provide valuable insights into how sleep impacts recovery in this patient population.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 60 who have sustained a traumatic brain injury and had no prior sleep disturbances.
Not a fit: Patients with a history of traumatic brain injury, mental illness, or sleep disorders, as well as those undergoing surgical intervention, will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery strategies for patients with traumatic brain injury by highlighting the importance of sleep patterns.
How similar studies have performed: While some studies have explored the relationship between sleep and recovery in TBI patients, this approach using wearable devices for objective data collection is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. 18\~60 years old. 2. The patient had no sleep disturbance problems prior to traumatic brain injury. 3. The patient has a definite diagnosis of traumatic brain injury and the Glasgow score is \>8. 4. The patient had abnormal imaging scans. 5. It has complete preclinical data. Exclusion Criteria: 1. Patients with a previous history of traumatic brain injury, mental illness, alcohol abuse or sleep disorders. 2. Patients admitted for surgical intervention. 3. Patients with a combination of other heavy visceral injuries. 4. Women during pregnancy and lactation. 5. The patents' use of medications that interfere with sleep
Where this trial is running
Yinchuan, Ningxia
- The General Hospital of Ningxia Medical University — Yinchuan, Ningxia, China (Recruiting)
Study contacts
- Study coordinator: Zhanfeng Niu, Doctor
- Email: niuzfeng228626@163.com
- Phone: +8613995297581
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.