Using white noise to improve sleep for hospitalized patients
Sleepless at Scripps: The Use of White Noise to Increase Sleep Duration in Hospitalized Patients, a Prospective Study
This study tests if using white noise can help older patients in the hospital sleep better by reducing the disturbances from hospital noise.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Scripps Health Academic / other |
| Locations | 1 site (La Jolla, California) |
| Trial ID | NCT05475262 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of white noise on sleep quality for hospitalized patients aged 65 and older. It employs a randomized cross-over design where participants will experience both active white noise (57-60 dB) and inactive white noise (45-50 dB) on alternate nights during their hospital stay. The primary outcomes include objective measurements of sleep duration and fragmentation, assessed using actigraphy devices. The goal is to determine if white noise can effectively reduce sleep disturbances caused by hospital noise.
Who should consider this trial
Good fit: Ideal candidates for this study are inpatient adults aged 65 years and older who are admitted to the internal medicine service for at least three nights.
Not a fit: Patients who are not hospitalized or those who do not meet the age and admission criteria may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance sleep quality for hospitalized patients, aiding in their recovery.
How similar studies have performed: Previous studies have indicated that sound management strategies, including white noise, can improve sleep quality in hospital settings, suggesting a potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Over 18 years old * Admitted to inpatient internal medicine service for at least 3 nights Exclusion Criteria: \-
Where this trial is running
La Jolla, California
- Scripps Health — La Jolla, California, United States (Recruiting)
Study contacts
- Study coordinator: Stuti Jaiswal, MD, PhD
- Email: JAISWAL.STUTI@SCRIPPSHEALTH.ORG
- Phone: 858-554-7909
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.