NCT06748950Not yet recruiting
Ketogenic Metabolic Therapy in Schizophrenia, Bipolar Disorder, Major Depressive Disorder: Deep Omic Profiling
A Randomized Controlled Trial of a Ketogenic Metabolic Therapy in Schizophrenia, Bipolar Disorder, Major Depressive Disorder: Deep Omic Profiling
Source: ClinicalTrials.gov · Last updated 16 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this randomized clinical trial is to be adequately powered to evaluate the effect of ketogenic metabolic therapy on the quality of life in serious mental illness, schizophrenia, bipolar disorder, major depressive disorder.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- First submitted
- 14 Dec 2024
- Start date
- Jul 2025
- Primary completion date
- Jul 2028
- Lead sponsor
- Stanford University
- Diseases
- Schizophrenia, Depression, Bipolar disorder
- NCT number
- NCT06748950
What you commit to
- Study type: Interventional
- Planned participants: 120
- From Jul 2025 to the primary completion date, Jul 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- participation in any clinical trial- within the past month or concurrent to study participation- with an investigational drug/device and/or intervention that may interfere with study participation/evaluation of results
Other illness
- severe renal or hepatic insufficiency
- cardiovascular dysfunction, including diagnosis of:
- Congestive heart failure
- Angina
- Arrhythmias
- Cardiomyopathy
- Valvular heart disease
- active substance abuse with illicit drugs or alcohol and/or current diagnosis of a Substance Use Disorder (Abuse or Dependence, as defined by DSM-IV-TR), with the exception of nicotine or cannabis dependence
- history of TBI
- any other medical condition that may make diet intervention dangerous as determined by the study medical team (e.g. anorexia nervosa) or assessed by study team to have insufficient control over their food intake to adhere to study diets.
- any medical condition that physicians or the PI believe would interfere with study participation or evaluation of results
- history of familial hypercholesterolemia
Other
- has started the ketogenic diet or was in ketosis within 3 months of wanting to enroll
- pregnant or nursing
- insulin dependent
- comorbidity of developmental delay
- in a current severe mood or psychotic state when entering the study that would prohibit compliance with study visits or dietary programs.
- any one who has been hospitalized or taken clozapine at doses above 550mg over the past 3 months
- inability to complete baseline measurements
- active suicidal and considered at significant risk for suicide during course of study
- mild BPRS at screening or baseline visits
Who the study is looking for
- diagnosed with bipolar disorder (BD), major depressive disorder (MDD), and or schizophrenia
- For individuals diagnosed with bipolar disorder (BD):
- Meet DSM V criteria for BD (any subtype)
- Not mild
- \>40 on BPRS
- clinically stable (with no hospitalization for past 3 months)
- For individuals diagnosed with major depressive disorder (MDD):
- Not mild
- PHQ-9 \> 10
- clinically stable (with no hospitalization for past 3 months)
- For individuals diagnosed with schizophrenia:
- Meet DSM V criteria for schizophrenia (any subtype)
- Not mild
- \>40 on BPRS
- clinically stable (with no hospitalization for past 3 months)
- Participants may currently be on a stable and adequate dose of SSRI antidepressant therapy or other psychiatric medication. Concurrent hypnotic therapy (e.g., with zolpidem, zaleplon, melatonin, or trazodone) will be allowed if the therapy has been stable for at least four weeks prior to screening and if it is expected to remain stable. Participants may be switched from other classes of medication to another medication class by their psychiatrist or primary care doctor, but need to be stable enough to enroll and adhere to study procedures.
- willing and able to give informed consent for participation in English.
- live within the United States.
- \--------------------------------------------------------------------------------
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Stanford University Coordinator of this site? Confirm its status | Palo Alto | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.