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NCT04299009 · ClinicalTrials.gov registry record · NA

Bright Light Therapy for Residual Daytime Symptoms Associated With Obstructive Sleep Apnea

A NA study, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT04299009: Completed NA study, sponsored by VA Office of Research and Development.

NCT04299009 is a NA study that has completed, run by VA Office of Research and Development. The registered enrollment target is 15 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04299009, a NA study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

Sleep apnea is one of the most common chronic condition among US military Veterans, causing sleepiness, reduced psychomotor vigilance and depression, which undermine daytime functioning and quality of life. Persistent daytime symptoms of sleepiness in individuals with Obstructive Sleep Apnea (OSA) who are using Continuous Positive Airway Pressure (CPAP) are associated with adverse long term medical and functional outcomes. Residual daytime sleepiness (RDS) is associated with reduced occupational and family functioning and overall lower quality of life. Napping is a common behavior among individuals with OSA and RDS and has been linked to both benefits to and decline in health and functioning. Longer nap times may maintain, as opposed to decrease, sleepiness by promoting sleep inertia and can contribute to maintaining subclinical circadian alterations that result in higher night-tonight variability in sleep patterns. Preliminary studies in humans and animal models have shown persisting alterations of circadian rhythms in OSA patients, that fail to normalize with CPAP treatment. CPAP treatment, while effective at correcting respiratory events and night time blood oxygen saturation levels, does not necessarily re-align the circadian system. Current treatment options are limited to stimulants and modafinil, whose long-term safety profile, effectiveness and impact on functional recovery is largely unknown. Supplementary exposure to bright light has beneficial effects on sleep quality and daytime vigilance in healthy individuals and it has been increasingly applied in a variety of sleep and neuropsychiatric conditions. However, no study to date has tested the application of BLT to treat daytime symptoms associated with sleep apnea. The investigators' study will be the first to explore the role of Bright Light Therapy (BLT), a well-established non-pharmacological intervention for circadian disturbances, for the treatment of residual daytime symptoms of OSA which do not res

Interventions

  • DEVICE Bright light therapy glasses

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2020-09-01
Est. Completion 2022-09-13
Phase NA

Sponsor

VA Office of Research and Development

1,668 total trials

What the Registry Record Tells You About NCT04299009

The ClinicalTrials.gov registry entry for NCT04299009 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bright light therapy glasses is the first listed.

NCT04299009 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04299009 about?

NCT04299009 is a clinical study titled "Bright Light Therapy for Residual Daytime Symptoms Associated With Obstructive Sleep Apnea". Sleep apnea is one of the most common chronic condition among US military Veterans, causing sleepiness, reduced psychomotor vigilance and depression, which undermine daytime functioning and quality of life. Persistent daytime symptoms of sleepiness in individuals with Obstructive Sleep Apnea (OSA) w...

What is the current status of trial NCT04299009?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2020-09-01. Estimated completion is 2022-09-13.

What interventions are being tested in trial NCT04299009?

The interventions under investigation include: Bright light therapy glasses (DEVICE).

Who is sponsoring clinical trial NCT04299009?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.