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Can meal timing and blue glasses tame mania? new pilot study explores Drug-Free options

NCT ID NCT06504342

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This pilot study tested whether time-restricted eating and blue-blocking glasses can help people with bipolar disorder during manic episodes. The goal was to see if these simple, drug-free approaches are feasible and safe for inpatients. Twenty-one participants were enrolled to track symptom changes and sleep-wake cycles, with results guiding a larger future trial.

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

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

21 people

The number who actually took part.

Started

Sep 2024

Finished

Oct 2025

Lead sponsor

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

16 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Be over age 16 * Have DSM-5-defined manic symptoms that persist beyond the physiological effects of a substance and a YMRS≥20 * Be willing to have investigators obtain information from the treatment team and electronic medical record * Participants must be able to read and understand English or French. * Be willing and able to provide informed consent. Exclusion Criteria: * Have a history of eating disorders. * Have a diagnosis of moderate to severe traumatic brain injury with residual or long-term effects, parenchymal brain surgery or stroke * Have a neurocognitive disorder * Take hypoglycemia-inducing medications * Be pregnant/lactating women * Have a diagnosis of sleep apnea * Have any other medical condition for which physician or investigator team expresses concern about safety or ability to participate in the study.

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Conditions

The condition(s) this trial relates to.

bipolar disorder Intermittent Fasting Mania

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Ottawa Hospital Research Insitute

    Ottawa, Ontario, K1Y 4E9, Canada

More trials for these conditions

Other studies related to the condition(s) this trial covers.