Can bright light beat insomnia? a new trial investigates
NCT ID NCT05715411
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether wearing light therapy glasses can help people with insomnia fall asleep faster. Adults aged 30 to 60 with insomnia will use the glasses or a placebo version, and researchers will measure sleep latency using actigraphy. The goal is to see if light exposure is a viable non-drug alternative to improve sleep onset.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- light therapy via portable glasses
- What this could lead to
- If effective, light therapy could offer a drug-free, easy-to-use treatment for insomnia, potentially helping many people who don't respond to current therapies.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to everyone. Light therapy may not improve sleep latency for all participants, and individual responses can vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 66 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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30 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient aged 30 to 60 years * Insomnia disorders (ICSD-3) with sleep latency \>30min - 3 times a week * Patient able to understand the objectives and risks associated with the research and to give informed dated and signed consent * Patient affiliated to a social health insurance scheme * For women of childbearing age, effective contraceptive measure for the duration of the research (hormonal contraception, IUD). Exclusion Criteria: * \- Shift work in the year preceding inclusion * Trans meridian travel (\> 2 time zones) in the month preceding inclusion * Patient in exclusion period determined by a previous or ongoing study * Impossibility of giving the patient informed information (emergency patient, difficulty understanding the patient) * Patient under judicial protection * Patient under guardianship or curatorship * For a woman of childbearing age: ongoing pregnancy or breastfeeding * Drug treatment which can disturb sleep or the measurement of DLMO: corticosteroids by general route, beta-blockers in the evening, exogenous melatonin. * Phase delay syndrome defined according to the criteria of the international classification of ICSD-3 * Restless legs syndrome with IRLS score\> 20 * Other psychiatric disorders or addictive disorder (screening with the MINI structured interview) * Other medical conditions not stabilized (detected by clinical interview), only the diseases appearing in the following list will constitute a criterion of non-inclusion: * Chronic allergies * Neurological disorders * cardiovascular, respiratory, gastrointestinal, hematopoietic, visual diseases * diseases of the immune system * kidney and urinary tract diseases * endocrine and metabolic diseases * infectious diseases * epilepsy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hôpitaux Universitaires de Strasbourg
RECRUITINGStrasbourg, 67000, France
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