Effects of sleep quality on recovery after heart surgery
The Effects of Non-pharmacological Interventions on the Quality of Sleep in Cardiac Surgical Patients
This study tests whether using eye masks and ear plugs to improve sleep can help adults recover better after heart surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Amrita Institute of Medical Sciences & Research Center Academic / other |
| Locations | 1 site (Kochi, Kerala) |
| Trial ID | NCT06527105 on ClinicalTrials.gov |
What this trial studies
This study investigates how sleep quality impacts recovery outcomes in patients undergoing elective cardiac surgery. It focuses on the use of eye masks and ear plugs to improve sleep in the intensive care unit (ICU) setting, where patients often experience sleep deprivation due to the hospital environment. By assessing the relationship between enhanced sleep quality and postoperative complications such as delirium and atrial fibrillation, the study aims to identify potential interventions that could improve patient recovery. The study will include adult patients aged over 18 years who are scheduled for cardiac surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients over 18 years old who are scheduled for elective cardiac surgery.
Not a fit: Patients with preoperative psychological disorders, those on mechanical ventilation for more than 12 hours, or those using sleep medications may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery outcomes and reduced complications for patients undergoing cardiac surgery.
How similar studies have performed: While the specific approach of using eye masks and ear plugs in this context may be novel, other studies have indicated that improving sleep quality can positively affect postoperative outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult cardiac surgical patients aged above 18years undergoing elective cardiac surgery Exclusion Criteria: * Not willing to give consent * Preoperative sleep medications use * Preoperative psychological disorders, on mechanical ventilation for \>12hrs, dementia, cerebrovascular accident
Where this trial is running
Kochi, Kerala
- Dr. Nagarjuna — Kochi, Kerala, India (Recruiting)
Study contacts
- Study coordinator: Nagarjuna P, MD, DM
- Email: drarjun83@gmail.com
- Phone: 9177208286
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.