Understanding sleep disturbances in ICU patients
Explore the Effects of SLEEP Deprivation on Short-term Outcomes in ICU pAtients basEd on polysomnogRaphy：a Single-center Prospective Cohort Study
This study looks at how sleep problems affect recovery in ICU patients to see if better sleep can help them heal faster.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Shanghai Zhongshan Hospital Academic / other |
| Locations | 1 site (Shanghai) |
| Trial ID | NCT06336408 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate sleep disturbances in patients admitted to the intensive care unit (ICU), focusing on the impact of sleep deprivation on patient outcomes. By utilizing polysomnography, the study seeks to provide a more accurate assessment of sleep quality compared to traditional subjective evaluation methods. The findings will help clarify how different levels of sleep disruption affect recovery and overall health in critically ill patients.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 years and older who are expected to stay in the surgical intensive care unit for 24 hours or more.
Not a fit: Patients who are pregnant, have a history of sleep disorder treatments, mental illness, or are undergoing specific treatments like CRRT or ECMO may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management of sleep disturbances in ICU patients, potentially enhancing their recovery and overall outcomes.
How similar studies have performed: While the approach of using polysomnography in ICU settings is gaining attention, this specific study addresses gaps in understanding sleep disturbances and their effects on critically ill patients, making it a novel exploration.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * adults (≥ 18-years old) * anticipated SICU stay for 24 hours or more Exclusion Criteria: * pregnancy * Have a clear history of medication for sleep disorders * History of mental or psychological illness * Treated with CRRT or ECMO during monitoring
Where this trial is running
Shanghai
- Zhongshan Hospital, Fudan University — Shanghai, China (Recruiting)
Study contacts
- Study coordinator: Jingjing Li, Master
- Email: li.jingjing@zs-hospital.sh.cn
- Phone: 13512106878
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.