Could a mood drug dull the Brain's reaction to light?
NCT ID NCT07750925
First seen Aug 06, 2026 · Last updated Aug 07, 2026 · Updated 1 time
Summary
This trial investigates whether taking lithium for a week changes how the eyes and brain respond to light in healthy adults aged 18 to 40. Participants will undergo light exposure sessions with and without lithium, while researchers measure melatonin suppression, alertness, mood, and brain activity. The study aims to uncover how lithium affects light sensitivity at the retina and in central pathways, which could shed light on its role in treating bipolar disorder.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lithium carbonate (Priadel)
- What this could lead to
- If lithium alters light responses, it could help explain how mood stabilizers work and why light therapy helps some people with bipolar disorder.
- What could go wrong
- This is a small, early study in healthy volunteers, not patients. Results may not apply to people with bipolar disorder, and lithium can have side effects.
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 45 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2029
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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18 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Aged between 18 and 40 years old * Fluent in English (both spoken and written) * Sleep duration between 6.5 and 9 hours daily * Have a regular normal sleep schedule with bedtime (weekdays) between 21:30 and 01:00. * BMI between 18 and 28kg/m2 * Currently enrolled and registered with a general practitioner * Female participants only: should use effective contraception or refrain from engaging in sexual activity that could result in pregnancy during participation in the study. Exclusion Criteria: * History of psychiatric or neurological disorders * First-degree family history of psychosis or severe mood disorder * Current or past suicidal ideation or self-harm * Current, chronic infections or diseases. * Life-threatening allergies, specifically a nut allergy. * Known visual disorders e.g., colour blindness, glaucoma, cataracts, diabetic retinopathy. * Known medical conditions that could affect the conduct of the study including * sleep disorders * cancer * diabetes * anaemia * epilepsy * psoriasis * thyroid disorders * kidney disease * severe eczema * anemia * migraines * Taking any long-term or regular medications other than oral contraceptives (e.g., antidepressants, diuretics (water-tablets), pain killers or anti-inflammatory drugs (such as ibuprofen) or medications for high blood pressure). * Have donated blood in the past 1 month * Regular or recent recreational drug use * Chronic alcohol addiction/misuse * Known contraindication to magnetic resonance imaging such as pacemaker or metal implants, recent surgery, severe claustrophobia and/or recent head or neck tattoos. * A current smoker (including use of cigarettes, vapes, and/or cigars). * Planning to travel across time zones at any point in time during the conduct of the study or have travelled across time zones within 1 month prior to enrolment. * Currently work night shifts * Been a shift worker in the past 3 months. * Current enrolment in any other interventional studies * Enrolment in any other interventional studies in the 1 month prior to the start of participation in this study
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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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Northumbria University
Newcastle upon Tyne, Tyne & Wear, NE1 8SG, United Kingdom
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