Recovery With Exogenous Ketones and Antipsychotics

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorUniversité de Sherbrooke

About this trial

The RECAP project will evaluate the clinical and metabolic effects of adding exogenous ketones to antipsychotic (AP) treatment in young adults with a first episode of psychosis (FEP).

FEP requires early intervention to limit relapse, chronic symptoms, cognitive decline, and reduced life expectancy. Symptoms include positive (hallucinations, delusions), negative (amotivation, anhedonia), cognitive (attention, working memory), and mood disturbances. Standard care combines second- or third-generation APs with psychosocial interventions. However, many patients have persistent symptoms despite optimal treatment.

Psychosis is linked to increased cardiovascular and obesity risk. APs can cause insulin resistance, type 2 diabetes, and dyslipidemia, but some metabolic abnormalities-both systemic and cerebral-may precede AP use, suggesting an intrinsic metabolic dysfunction. Brain energy metabolism is often impaired, with altered insulin signaling, glucose transport, and ATP production. Glucose hypometabolism in the prefrontal cortex correlates with negative and cognitive symptoms, even before medication, resembling patterns in Alzheimer's, bipolar disorder, and depression.

Ketones, especially beta-hydroxybutyrate, provide an alternative to glucose for brain energy. Ketogenic diets have therapeutic potential but are difficult to maintain, particularly in psychiatric populations. Exogenous ketones, such as medium-chain triglycerides (MCTs), can raise circulating ketone levels without major dietary changes. MCT supplementation has been shown to improve brain metabolism and cognition in other conditions, but no studies have tested it in FEP.

This uncontrolled, prospective pilot study will provide 15 g of MCT oil twice daily for 12 weeks, in addition to participants' usual diet and treatment. The primary objective is to assess changes in circulating ketone levels and metabolic markers (glucose, insulin, HbA1c). Secondary objectives include feasibility, acceptability, effects on real-time glucose metabolism (via continuous glucose monitoring), clinical symptoms (negative, cognitive), quality of life, other metabolic biomarkers, and general systemic markers.

This is the first study to test exogenous ketones in FEP. It will assess safety, tolerability, and potential metabolic and clinical benefits, offering preliminary mechanistic insights and guiding future integrative mental health strategies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Referred or self-referred to the PEP Clinic of the Estrie region, either as an outpatient or inpatient.

Currently receiving a second- or third-generation antipsychotic at a stable dose for at least 4 weeks.

Able to read and communicate in French or English.

Capable of understanding and signing the informed consent form.

Disqualifiers

Pregnancy, childbirth within the past 6 months, or breastfeeding.

any use of MCT oil, ketone salts, or a ketogenic diet within the past year.

Previous diagnosis of type I or type II diabetes.

Uncontrolled acute suicidal ideation at the time of inclusion in the PEP clinic.

Trial design

Design model

Single group

Treatments tested in this trial

  • Medium chain triglyceride oil

    Other intervention

    Supplementation with 15 g of medium chain triglyceride oil, a food product commercially available over-the-counter in regular grocery stores, emulsified in beverage of choice, twice daily (morning and evening) for 12 weeks.

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: 12 week ketogenic supplementationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Plasma total ketones concentration

Change in plasma total ketone (acetoacetate + betahydroxybutyrate) after 12 weeks of supplementation (uM)

Time frame
12 weeks
2

Plasmatic glucose concentration

Change in glucose concentration (mM) after 12 weeks of supplementation (uM)

Time frame
12 weeks
3

Plasma Insulin concentraiton

Change in insuline concentration (UI) after 12 weeks of supplementation (uM)

Time frame
12 weeks
4

Plasma Glycated hemoglobin

Change in Glycated hemoglobin (%) after 12 weeks of supplementation

Time frame
12 weeks

Secondary outcomes

1

acceptability of exogenous ketone supplementation

Participant perspectives will be collected through a short semi-structured interview and analyzed using a descriptive thematic approach.

Time frame
at the end of the 12 weeks treatment
2

compliance rate

dose of supplement taken during the 12 weeks/ number of dose expected (%)

Time frame
during 12 weeks intervention
3

Adverse event rate

Total number of adverse event during the intervention

Time frame
12 weeks intervention
4

Drop-out rate

Number of participant taht have drop-out/total number of participant included in the study

Time frame
After 12 weeks of intervention

Other outcomes

Sponsors and contacts

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