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| Name | Class |
|---|---|
| TriService Nursing Research Program | OTHER |
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Human centric lighting (HCL) is a technology that supports the body's circadian rhythm, as it can stimulate the sleep triggering hormone, melatonin, to improve sleep hygiene over standard lighting (SL), and promote recuperative sleep for a timely return-to-duty. In intensive care units, exposure to HCL has improved sleep measures. However, the effect in the medical surgical (MS) environment is unknown. The purpose of this study is to assess the feasibility of study procedures in MS setting and conduct a preliminary evaluation of the effect of light on inpatient sleep. Recruitment started November 2020 through April 2021. Data analysis is pending.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Human Central Lighting (HCL) Room | Experimental | This inpatient room was outfitted with lights that mimic the day/night cycle, thereby supporting circadian rhythm. Day time lights were automatically on during 0600 to 1900 and in use any time the patients would normally utilize their lights, with a goal of three hours of light exposure per day. The lights automatically transitioned to warmer toned evening lighting at 1900. |
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| Standard Hospital Lighting (SL) Room | No Intervention | The lighting in this room was standard florescent hospital lighting. The only changes in the lighting was the on/off settings normally associated with lighting. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Human Centric Lights | Device | Bright light is emitted during the day from 06:00, then auto-dimmed light is used at night, beginning 19:00. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Total Sleep Time | Assess the feasibility of measuring total sleep time in MS setting, using an actigraphy device. | During participant's inpatient stay, not to exceed 5 days. |
| Sleep Efficiency | Assess the feasibility of measuring sleep efficiency in MS setting, using an actigraphy device. | During participant's inpatient stay, not to exceed 5 days. |
| Sleep Patterns | Assess the feasibility of assessing sleep patterns in MS setting, using a Consensus Sleep Diary (CSD). | During participant's inpatient stay, not to exceed 5 days. |
| Dim Light Melatonin Onset - collection | Assess the feasibility of collecting samples to assess dim light melatonin onset in MS setting, using passive drool saliva sampling. | During participant's inpatient stay, not to exceed 5 days. |
| Patient experience | Describe the patient's experience of participating in the study, in a MS setting, using a semi-structured interview (SSI). | One time - approximately a 5 to 15 minute interview |
| Measure | Description | Time Frame |
|---|---|---|
| Dim Light Melatonin Onset - analysis | Conduct a preliminary evaluation of the effect of light on inpatient sleep using dim light melatonin onset saliva sampling. | Collected during participant's inpatient stay, not to exceed 5 days. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pauline A Swiger, PhD | US Army Landstuhl Regional Medical Ceneter | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Landstuhl Regional Medical Center | Landstuhl | Germany |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Aug 14, 2025 | |
| Reset | Sep 3, 2025 |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | Mar 30, 2021 | Jun 24, 2021 | ICF_000.pdf |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Aug 14, 2025 | Sep 3, 2025 |
| ID | Term |
|---|---|
| D020447 | Parasomnias |
| ID | Term |
|---|---|
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
| D001523 | Mental Disorders |
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