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 volunteersQualifiers
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
Single group
Treatments tested in this trial
Medium chain triglyceride oil
Other interventionSupplementation 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
Trial outcomes
Primary outcomes
Plasma total ketones concentration
Change in plasma total ketone (acetoacetate + betahydroxybutyrate) after 12 weeks of supplementation (uM)
Plasmatic glucose concentration
Change in glucose concentration (mM) after 12 weeks of supplementation (uM)
Plasma Insulin concentraiton
Change in insuline concentration (UI) after 12 weeks of supplementation (uM)
Plasma Glycated hemoglobin
Change in Glycated hemoglobin (%) after 12 weeks of supplementation
Secondary outcomes
acceptability of exogenous ketone supplementation
Participant perspectives will be collected through a short semi-structured interview and analyzed using a descriptive thematic approach.
compliance rate
dose of supplement taken during the 12 weeks/ number of dose expected (%)
Adverse event rate
Total number of adverse event during the intervention
Drop-out rate
Number of participant taht have drop-out/total number of participant included in the study
Sponsors and contacts
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