Abstract
Background
Serious mental illness imposes a substantial burden. Pharmacologic treatments remain only partially effective and are associated with significant side effects, highlighting the need for novel treatment approaches. Ketogenic metabolic therapy (KMT) is emerging as an intervention for serious mental illness, with a growing evidence base and strong patient interest. A critical barrier to KMT implementation is the lack of health care professional (HCP) competence and readiness to discuss KMT with patients with serious mental illness. Existing training does not adequately address HCP competence in presenting KMT as a treatment option. This study describes the pilot-testing of “Live It, Launch It” (LI-LI), the first KMT training program designed to build self-reported competence to discuss KMT in psychiatric care for HCPs.
Methods
LI-LI combines a 4-hour asynchronous educational course on KMT with a 4-week experiential group KMT intervention during which participants adhered to a ketogenic diet. LI-LI aimed to improve self-reported competence to utilize KMT and perceived ability to engage in shared decision-making with patients about incorporating KMT into their treatment plan.
Results
Forty HCPs participated in the education course: 10 psychiatrists, 10 psychiatric pharmacists, 8 psychologists/therapists, and 12 other HCPs (e.g., nurse practitioners, physician assistants). Twenty-five initiated the diet intervention. Baseline competence scores (visual analog scale 0-100) were low, M(SE) = 17.40 (2.68), increasing to M(SE) = 68.08 (2.47) after education (d = 2.88, p <0.0001), and to M(SE) = 86.62 (1.82) post-diet (d = 1.08), with a very large whole-study effect (d = 3.49, p < 0.0001). Shared decision-making scores at baseline were M(SE) = 53.64 (2.89), increasing to M(SE) = 83.35 (1.83) after the educational course (d = 1.74, p <0.0001), and to M(SE) = 91.23 (2.05) after the diet phase (d = 0.73, p = 0.009), with a very large whole-study effect (d = 2.53, p < 0.0001). Feedback indicated that lived experience with KMT was helpful for implementation-readiness.
Discussion
The educational course on KMT was associated with increased self-reported competence and perceived shared decision-making in HCPs, and this was enhanced with combined education and lived experience. Implementation of this approach could accelerate KMT into clinical care. Results should be interpreted with caution as this was a small uncontrolled study with self-reported main outcomes.
Clinical trial registration
https://clinicaltrials.gov/study/NCT07116226, identifier NCT07116226.
Keywords: competence, shared decision-making, health care professionals, ketogenic diet, mental health, training model, ketogenic metabolic therapy, education
Background
According to the World Health Organization (WHO), nearly 1 billion people worldwide were living with a mental disorder in 2019, underscoring the vast global burden of mental illness (1). The economic impact is similarly profound; for example, the societal cost of schizophrenia alone in the United States was estimated at $366.8 billion in 2024 (2). Existing pharmacologic treatments are often only partially effective and frequently associated with significant adverse effects (3–12). These adverse effects contribute to poor adherence or treatment discontinuation, increasing the risk of relapses and suicide (11, 13, 14). In addition, current clinical guidelines provide limited support for individualized medication selection partially due to lack of understanding underlying pathophysiology and disease subgroups (15). As a result, psychopharmacologic treatment often relies on a trial-and-error approach to balance therapeutic benefits and tolerability (16).
Individuals with serious mental illness experience disproportionately high rates of medical comorbidities, including obesity, type 2 diabetes, cardiovascular disease, and metabolic syndrome, all of which contribute substantially to disability, reduced quality of life, and escalating healthcare expenditures (17–19). These comorbidities arise from such factors as social determinants of health, lifestyle choices, chronic stress, psychotropic medication effects, and potentially shared biological mechanisms linking metabolic and psychiatric dysfunction (20, 21). As a result, people with serious mental illness die 10–20 years earlier than the general population, with the majority of mortality attributable not to suicide, but to preventable and treatable chronic medical illnesses, particularly cardiometabolic disease (22). In addition to the significant human burden, these overlapping psychiatric and medical conditions contribute to markedly increased healthcare utilization and economic costs across inpatient, outpatient, emergency, and long-term care settings (19, 23).
The limited efficacy of available treatments, along with the need to simultaneously address physical health comorbidities, have driven efforts to identify novel and more acceptable treatment options. Increasingly, systems, patients, families, and caregivers are requesting focus and attention on alternative and holistic treatments beyond or in addition to traditional pharmacologic interventions (24–30).
One emerging potential treatment is the use of a ketogenic diet for medical treatment, also referred to as ketogenic metabolic therapy (KMT). This growing body of evidence suggests that metabolic dysfunction may contribute to psychiatric disorders and that the state of ketosis may represent a novel therapeutic mechanism for treatment (31, 32). KMT is a well-established treatment for epilepsy, with over a century of supporting evidence (33, 34). In the context of KMT for epilepsy, macronutrient ratios are typically 3:1 or 4:1 grams of fat to combined protein and carbohydrates (34). Emerging data on KMT in psychiatric populations, is being used in modified ratios typically between 1:1-2.5:1 grams of fat to combined protein and carbohydrates (see 35, 36-40).
Early studies using KMT for mental illness show promising symptom improvements in schizophrenia, bipolar disorder, and depression (35–42). The first randomized controlled trial for KMT in serious mental illness has recently been published, which found metabolic improvements in participants with bipolar and schizophrenia after 1 month on KMT compared to diet-as-usual controls, and found significant improvement in positive, negative, cognitive, and depressive symptoms in participants on KMT for 4-months (36). Importantly, the study phase that showed significant psychiatric improvement was single-arm (36). Therefore, we still need randomized controlled trials testing psychiatric improvement on KMT for sufficient durations of time in order to have gold standard evidence for KMT in psychiatric care. Another randomized controlled trial that is designed to do this is currently finalizing (43). In addition to psychiatric improvement, KMT may be useful in attenuating common metabolic health comorbidities observed in people with serious mental illness, such as metabolic syndrome, insulin resistance, and type 2 diabetes (44–46).
While further research is needed, clinical recommendations have recently been published supporting the use of KMT alongside standard care in psychiatry (47). However, preparation for improving knowledge about KMT will likely be insufficient to change prescribing and implementation behaviors. Many treatments in psychiatry, despite an adequate evidence-base, remain slow to be adopted and often remain underutilized, as is the case with clozapine, long-acting injectable antipsychotics and lithium, three effective and underused treatments (48–51). Barriers for implementation into practice are multifactorial but often include the fact that health care professionals (HCPs) report lack of competence/confidence in using new or more complex treatments (52–54). Changing prescribers’ behaviors has been a major challenge and scientific focus using many traditional educational approaches, such as dissemination of printed educational materials, academic detailing, and continuing education workshops to improve knowledge of the topic. Nonetheless, these strategies have been shown to be insufficient in changing clinician behavior or improving patient outcomes (55, 56). More active strategies such as audits and feedback, or educational outreach visits, show only modest effects in changing behaviors beyond educational strategies and remain limited in their impact (57, 58).
Successful implementation of a new treatment modality into practice depends on three key elements: evidence, context, and facilitation (59). Facilitation involves the processes and strategies used to guide and support HCPs throughout the implementation process, helping to overcome barriers and promote the successful adoption of the new treatment. These elements are strengthened through immersive, or hands-on experiential learning approaches which have been shown to improve learner engagement, knowledge, retention, and confidence, the latter which is known to be a more reliable predictor of behavior change (60–62). Educational theory further emphasizes the importance of self-efficacy in promoting behavior change. Self-efficacy refers to an individual’s belief in their ability to successfully perform a task such as prescribing or using new treatments (63). Closely related to this concept is competence, or a clinician’s perceived ability to implement a task, which serves as an important mediator or driver of behavior change and adoption of new practices (64, 65). Our previous work has focused on strategies to improve competence for improving psychiatric treatment implementation (66).
We therefore investigated whether an educational program incorporating active participation and lived experience designed to facilitate how to plan, initiate, and monitor a ketogenic diet, would improve HCP self-reported competence for using a ketogenic diet with patients. “Live it Launch it” (LI-LI) is a training model designed to enhance HCP self-reported competence and confidence in shared decision making with their patients specifically with regards to implementing KMT for mental illness. Given growing evidence, patient demand and limited HCP training, this study aimed to assess whether immersive education could improve HCP self-reported competence (rather than objective assessment) to incorporate this emerging treatment into clinical practice.
Methods
Design
This study was a single-arm open-label pilot trial that employed a two-part training model. The first component consisted of an online educational intervention about KMT for mental health (described in Supplementary Table 1) (educational phase), and the second phase was a 4-week lived cohort experience in which participants implemented the ketogenic diet themselves (diet phase). This yielded a total of 3 study timepoints (pre-education/baseline, post-education/midpoint, and post-diet/endpoint).
Participants
HCPs from across the United States were recruited, and the first 40 eligible individuals were enrolled. Eligibility criteria for the educational component included age 18–74 years, not currently following a ketogenic diet, no prior successful personal implementation of a medical ketogenic diet, and active involvement in clinical care or research as an HCP. Target enrollment was N = 30 but permitted up to N = 40. Forty participants completed the educational phase, and 21 of these participants also completed the diet phase.
Eligibility for participation in the dietary intervention included ages 18–74 years, body mass index >18.5 (self-reported), not currently on KMT, and no prior successful experience implementing a ketogenic diet. Exclusion criteria included pregnancy or lactation, type 1 diabetes, insulin-dependent type 2 diabetes, or diagnosed carnitine deficiency.
All participants met with a research coordinator either in person or via Zoom to review study procedures and provide informed consent. Participants completed the Evaluation to Sign Consent (ESC) to assess decisional capacity, and written informed consent was obtained electronically (Docusign®) or in person. The study protocol was approved by the University of Maryland Institutional Review Board.
Materials
Educational coursework
All participants were asked to complete the same educational program. The educational content was delivered through the Ketogenic Metabolic Therapy for Psychiatric Conditions course (67). Specifically, this was a 4-hour asynchronous course consisting of four modules covering foundations of KMT such as its history and illness application and how glucose, ketones, and insulin work; variations and personalization of KMT such as the classic versus modified ketogenic diet; how to do a well-formulated ketogenic diet, which aims to optimize overall nutrition on the ketogenic diet; and ketogenic management, such as monitoring labs and addressing adverse effects (See Supplementary Table 1). The course also included a substantial library of optional supplemental resources, including quizzes, scientific literature, case studies, patient interviews, educational videos, implementation guides, food lists, KetoDietCalculator tutorials, resource directories, and additional condition-specific learning materials. This course is available to the public for $299 but was provided at no cost to participants as part of the study. No continuing medical education (CME) credits were offered; however, continuing education units (CEU) were available for Registered Dietitian Nutritionists (RDNs).
Diet intervention
After a 2-hour meeting with an RDN or nutrition specialist physician, participants were instructed to initiate a medical ketogenic diet with a target macronutrient ratio ~1.5:1 (grams of fat to combined grams of carbohydrate and protein), but could range from 1:1 to 2.1, depending on individual ability to reach ketosis. Individual daily caloric requirements were calculated in collaboration with an RDN or nutrition specialist physician, incorporating age, sex, weight, height, activity level, and individual goals (e.g., maintaining vs. losing weight). Macronutrient ratios and caloric targets were adjusted throughout the intervention to optimize ketosis, support weight goals, and ensure adequate protein intake. Participants were able to choose between a precision ketogenic diet, in which a gram scale is used to weigh food, or a modified ketogenic diet, in which measuring cups and measuring spoons are used.
Participants were responsible for implementing the diet independently using standardized guidance provided during the educational program, supplemented by individualized recommendations from the RDN or nutrition specialist physician. All participants began the intervention within the same 7-day window and followed dietitian-prescribed caloric targets (e.g., 2000–2200 kcal/day). Nutritional plans were individualized and ranged from two meals per day to three meals and 2 snacks per day. Ongoing support was provided by the lead RDN, who assisted with calculating macronutrient distributions and making iterative adjustments during the study period.
Participants tracked dietary intake using the Cronometer® application (Gold version), which was provided to them at no cost (68). The goal was to achieve and maintain nutritional ketosis, defined as blood β-hydroxybutyrate (βHB) levels ≥0.5 mmol/L, with an expected range of 1–5 mmol/L for most participants. To track βHB, KetoMojo® glucose and ketone monitors were provided to participants at no cost. Food scales were provided as needed to support accurate measurement of intake, also at no cost to participants. More details on diet-related materials will be provided in another publication.
Participants were encouraged to review medications for carbohydrate content, particularly liquid formulations. Reporting medications was optional to respect participant privacy. A daily multivitamin was recommended, and additional supplementation (e.g., vitamin D, calcium) was advised at the discretion of the RDN or nutrition specialist physician. Further dietary details and specific health outcomes using the diet, such as macronutrients, micronutrients, βHB, health outcomes, and side effects, will be reported in another paper.
Clinical assessments
At baseline, participants completed demographic information and two self-efficacy-based assessments.
Self-reported competence
The primary outcome was self-reported competence. This construct is grounded in self-efficacy and defined in this study as a participant’s perceived ability to implement KMT in patients with mental illness (65). Consistent with established measurement approaches for assessing self-reported competence as described above and our experience using this as an outcome in educational interventions (65, 66, 69), we assessed self-reported competence using a Visual Analog Scale (VAS) ranging from 0–100 mm, with anchors of 0 (no competence) and 100 (fully competent). Overall self-reported competence was measured by the question “How competent are you at implementing a ketogenic diet?” Additionally, 14 additional sub-items were asked relating to various specific aspects of the process, including monitoring ketones, assessing side effects, etc. (Full questions are in Supplementary Table 2). Self-efficacy ratings have demonstrated strong reliability and validity in assessing perceived competence (61, 70, 71).
Self-efficacy of shared decision making
A secondary outcome was perceived shared decision making ability with patients, which refers to HCPs’ level of confidence in supporting their patients in making an informed choice and using a ketogenic diet in the future. The Decision Self-Efficacy Scale (DSE), a validated and reliable 11-item self-report instrument (72–74), was used to evaluate confidence in shared decision making. The DSE is rated on a 5-point Likert-type scale ranging from 0 (not at all) to 4 (very confident). This measure was used to evaluate HCP readiness to incorporate KMT into patient-centered care discussions. See the list of items in Supplementary Table 3.
Exploratory qualitative data
At the conclusion of the study, we asked if participants thought that LI-LI improved their ability to implement a ketogenic diet. We also asked questions on what aspects of learning helped them the most, what aspects surprised them, and what they would change about the educational program. Additionally, many participants also included many discussion points they would want to emphasize with their patients. We also asked about clinical populations for which participants were interested in using KMT.
All study data were collected and managed using the REDCap system. Participants were asked open-ended questions regarding the most helpful aspects of the program to collect rich qualitative data that may pick up information the questionnaires did not. Qualitative analysis was conducted in accordance with methods for thematic analysis by Braun & Clarke (2006) and following the specific steps outlined by Ahmed (2025). Broadly, responses were read multiple times and initial impressions were noted; initial codes were generated upon later reads; candidate themes were recorded; and final themes were chosen (See Supplementary Table 4).
Procedure
After providing informed consent, participants received a link to complete baseline assessments, including measures of self-reported competence and shared decision making. These questionnaires were administered through REDCap. After participants completed baseline assessments, the educational intervention began. The education phase included 4-hours of online asynchronous course curriculum; two 1.5-hour educational sessions available to all national course participants; and three weekly one-hour free form Q&A sessions with the lead Registered Dietitian Nutritionist (RDN), which were provided exclusively to LI-LI study participants following diet initiation. Participants were given approximately one month to complete baseline assessments, online training, and post-education assessments of self-reported competence and shared decision making for future use with patients. After completing the post-education assessments, participants were invited to continue into the experiential diet phase of the study and implement KMT themselves as part of a cohort experience (living out the diet). This phase consisted of an initial 1–2-hour individual consultation with a dietitian or nutrition specialist physician, followed by a 4-week self-implemented ketogenic diet as a cohort. During this period, participants were invited to attend a weekly live group-based Q&A with the lead study dietitian and each other to ask questions about the diet, share recipes and strategies, and ask about side effect management. After the 4-week diet experience, participants completed endpoint assessments of self-reported competence and shared decision making. More details on the diet phase of the study, including food tracking, health outcomes, detailed side effect coverage, and qualitative feedback on living out the diet, will be published elsewhere.
Analysis of data
This pilot trial was designed to inform a larger implementation study. The pre-to-post educational study included the sample of N = 40, and pre-to-post-diet changes included the diet completers (N = 21). Pre-to-post changes in 100 mm VAS scores measuring self-reported competence for the educational program as well as perceived shared decision making using the DSE scale were calculated using linear mixed-effects models. Time was included as a categorical fixed effect with three levels, and a participant-specific random intercept was included to account for within-participant correlation among repeated measurements. Under the assumptions of independent and homoscedastic residual errors, this mixed-effects model specification induces a compound-symmetry marginal covariance structure within participants. Models were estimated using restricted maximum likelihood (REML), with degrees of freedom approximated using the Satterthwaite method. All available observations were included without restricting the analyses to participants with complete data at all time points. Follow-up pairwise comparison between time points were conducted using estimated marginal means. Qualitative responses were analyzed using thematic analysis (75), and the 16-item checklist for this process was followed to ensure rigorous application of this method (76).
Results
The study opportunity was posted using an IRB approved graphic via the Maryland Psychiatric Research Center (MPRC) social media pages (LinkedIn, Instagram and X) and reached full enrollment (N = 40) within two weeks. One participant withdrew shortly after consenting due to an unrelated hospitalization and was replaced prior to study initiation. A CONSORT diagram is presented in Figure 1. Of the 40 enrolled participants, 26 elected to continue into the diet phase. Reported reasons for non-participation in the diet phase included pregnancy or plans for pregnancy (n=4), scheduling conflicts (n=4), unspecified reasons (n=4), dietary restrictions (n=1), and concerns about side effects (n=1). One was excluded from the diet phase before it began due to low BMI.
Figure 1.

Participant flow CONSORT diagram.
The sample included approximately 25% physicians, 25% pharmacists, 20% psychologists/therapists, and 30% other health professionals (including nurses, physician assistants, nurse practitioners, and researchers). All participants (N = 40) completed the educational component. See Table 1 for participant demographics. Among those entering the diet phase, 21 of 25 participants (84%) completed the full 4-week intervention. One participant was excluded after enrollment for not meeting eligibility criteria; one was unable to start with the cohort; and two were withdrawn due to adverse events, which were believed to be related to the diet and were rated as moderate (muscle soreness, heart palpitations). The person with muscle soreness withdrew after 3 weeks on the diet and did not reach resolution by the end of the 4-week study despite diet discontinuation the week prior. The person with heart palpitations withdrew after 2 weeks on the diet and reported resolution after discontinuing the diet and medium-chain triglycerides (MCT) oil. Diet benefits, tolerability, adverse effects, and laboratory values associated with the diet in N = 21 will be discussed in further detail in another publication.
Table 1.
Demographic information.
| Education phase (N = 40) |
Diet phase (N = 21) |
|
|---|---|---|
| Sex | N (%) | N (%) |
| Female | 29 (72.5%) | 15 (71%) |
| Male | 11 (27.5%) | 6 (29%) |
| Race | ||
| Black | 5 (12.5%) | 2 (10%) |
| White | 30 (75%) | 16 (76%) |
| Asian | 4 (10%) | 2 (10%) |
| Multiracial | 1 (2.5%) | 1 (5%) |
| Profession | ||
| Pharmacists | 10 (25%) | 7 (33%) |
| Physicians | 10 (25%) | 2 (10%) |
| Psychologists/Therapists | 8 (20%) | 3 (14%) |
| Other | 12 (30%) | 9 (43%) |
| Age | Mean (SD) | Mean (SD) |
| 44.41 (9.16) | 46.59 (7.08) | |
Q & A group session attendance
During the educational phase, one national Q&A session was offered, which was a group session open to all patients under AKT, Limited Liability Company (LLC) care including the study participants, with 8 of 40 participants (20%) attending. A second Q&A session for just LI-LI study participants was offered during the diet phase and was attended by 18 of 40 participants (45%). Among those in the diet cohort, attendance at weekly study-specific Q&A group sessions was as follows: baseline (18/25; 72%), week 1 (14/24; 58%), week 2 (11/22; 50%), and week 3 (13/21; 62%). Out of the 21 diet completers, 18 (86%) went to at least one study-specific diet group meeting.
Main outcomes
Self-reported competence
Overall self-reported competence on the VAS scale from 0 to 100 was M(SE) = 17.40 (2.68) before education (baseline), M(SE) = 68.08 (2.47) after education, and M(SE) = 86.62 (1.82) after the diet phase. A linear mixed model and follow-up specific comparisons showed statistically significant improvements in self-reported competence at every time point and spanning the whole study (see Table 2). From pre-education to post education, improvements were significant, p < 0.0001, with a large effect size, d = 2.88, 95% CI [2.17, 3.58]. From post-education to post-diet, improvements were also statistically significant, p < 0.0001, with a large effect size, d = 1.08, 95% CI [0.52, 1.61]. The total effect, spanning the whole study from pre-education to post-diet, was largest and most significant, p < 0.0001, d = 3.49, 95% CI [2.33, 4.63]. Improvements in self-reported overall competence across all three timepoints (pre-education, post-education, and post-diet) are visualized in Figure 2. An exploratory visualization of individual aspects of self-reported competence over the three timepoints are shown in Figure 3 to describe specific areas of KMT which participants felt they had improved.
Table 2.
Linear mixed model for overall self-reported competence rating at each time point.
| Linear mixed model Model reference timepoint: Pre-education | |||||
|---|---|---|---|---|---|
| Estimate | SE | Df | t | P-value | |
| Intercept (pre-education) | 17.40 | 2.39 | 84.16 | 7.29 | <0.0001 |
| Post-education | 50.68 | 2.81 | 56.78 | 18.00 | <0.0001 |
| Post-diet | 68.07 | 3.51 | 65.59 | 19.38 | <0.0001 |
| Specific comparisons | |||||
| Pre-education to post-education | 50.7 | 2.81 | 59.4 | 18.01 | <0.0001 |
| Post-educatiom to post-diet | 17.4 | 3.53 | 67.9 | 4.93 | <0.0001 |
| Pre-education to post-diet (whole study effect) | 68.1 | 3.53 | 67.9 | 19.28 | <0.0001 |
Figure 2.

Self-reported overall competence for the implementation of a ketogenic diet (visual analog scale 0 – 100).
Figure 3.

Self-reported competence for individual aspects regarding the ketogenic diet.
Self-reported shared decision making
Perceived decision making self-efficacy to use KMT, as measured by the DSE, was M(SE) = 53.64 (2.89) at baseline. Post-education phase, average DSE was M(SE) = 83.35 (1.83). Post-lived experience on KMT, DSE level was improved to M(SE) = 91.23 (2.05). A linear mixed model and follow-up specific comparison showed statistically significant improvements in DSE at every timepoint across the whole study (See Table 3). Improvements from pre-education to post-education were statistically significant (p < 0.0001), with a large effect size, d = 1.74, 95% CI [1.24, 2.23]. Improvements from post-education to post-diet were statistically significant (p = 0.009), with a moderate-large effect size, d = 0.73, 95% CI [0.24, 1.20]. The total improvement in DSE scores from baseline to post-diet, was statistically significant (p < 0.0001), with a large effect, d = 2.53, 95% CI [1.63, 3.41] (See Figure 4).
Table 3.
Linear mixed model for shared decision making self-efficacy score, as measured by the DSE, over all three timepoints.
| Linear mixed model Model reference timepoint: Pre-education | |||||
|---|---|---|---|---|---|
| Predictor (time point) | Estimate | SE | Df | t-value | P-value |
| Intercept (pre-education) | 53.64 | 2.28 | 80.94 | 23.54 | <0.0001 |
| Post-education | 29.72 | 2.61 | 56.42 | 11.38 | <0.0001 |
| Post-diet | 38.59 | 3.27 | 64.53 | 11.80 | <0.0001 |
| Specific comparisons | |||||
| Estimate | SE | Df | T | P-value | |
| Pre-education to post-education | 29.72 | 2.61 | 59.3 | 11.38 | <0.0001 |
| Post-education to post-diet | 8.87 | 3.29 | 67.2 | 2.70 | 0.009 |
| Pre-education to post-diet (whole study effect) | 38.59 | 3.29 | 67.2 | 11.74 | <0.0001 |
Figure 4.

Self-reported shared decision making scores using the decision self-efficacy (dse) scale (0-100).
Exploratory outcomes
Qualitative data
At study completion, 29 participants provided qualitative feedback on the program. Twenty-eight out of 29 (97%) answered “Yes” to the question “Do you think the Live It Launch It program improved your ability to implement a ketogenic diet for your patients?” Supplementary Table 4 lists thematic codes identified in the open-ended qualitative responses and broader themes formed based on these codes through thematic analysis (75). These questions included helpful aspects and improvements they would make to the educational program and what discussion points they would want to emphasize with their patients, as well as expected challenges for patients implementing KMT.
Also, at the start of the study, participants completed a checklist of the clinical populations for which they may have interest in using a ketogenic diet. Figure 5 shows the total number of HCPs (out of 40) who indicated potential interest in using KMT for each diagnosis.
Figure 5.

Clinical diagnoses for which health care professionals may have future interest in considering ketogenic diets for treatment (N = 40)*. *Evidence base for treatments is variable for each condition. This question provided understanding of potential future use and not a measure of efficacy, effectiveness or strength of evidence base.
Discussion
To our knowledge, this is the first study to evaluate a KMT training program designed to improve HCP self-reported competence in introducing, offering, and discussing KMT in psychiatric care for individuals with serious mental illness. LI-LI is distinctive as it is also the first KMT training program to integrate training to enhance shared decision making in HCPs. Given the complexity of implementing dietary interventions in psychiatric care and the growing concerns that the current workforce is inadequately prepared to deliver such interventions (77), there is a need to train a variety of multidisciplinary HCPs in KMT for mental health. These findings demonstrate that LI-LI was associated with improved self-reported competence in HCPs to discuss and offer KMT and improved self-reported shared decision making capability to collaborate with patients in considering KMT as part of their treatment.
The demand for training was high, with enrollment reaching capacity within two weeks and participation spanning multiple disciplines, including physicians, pharmacists, therapists, and other HCPs. This multidisciplinary engagement is particularly encouraging given the collaborative nature of psychiatric care and ongoing workforce shortages (78–80). It is important to point out that certain HCPs can prescribe and monitor KMT themselves (e.g. physicians and RDNs), while others (e.g., psychologists, therapists, researchers) would be able to educate patients about KMT and then refer them to an appropriate specialist (e.g., RDN) for implementation and monitoring. We believe that educating people in diverse HCP roles is important, as this will increase patient reach, awareness, and knowledge of KMT, even if an additional provider is needed to monitor and implement the diet. The goal of these efforts is to ultimately increase patient access and choice, even if it takes a more collaborative care approach.
Considering the high levels of competing demands inherent to a sample of HCPs, participant engagement was strong. A slight majority completed the lived experience diet phase (21/40; 53%) and within the diet phase, most attended at least one group Q&A session (18/21; 86%).
Large and significant improvements in self-reported competence emerged after participation in LI-LI (Table 2). Meaningful changes on VAS are often in the range of 13–15 points (81–84), so the observed increase of 69.2 points overall represents a substantial effect. Mean self-reported overall competence scores were ~87 after the lived diet experience, signifying high self-perceived confidence in the learned skills. The data suggests that both KMT education and self-implementation were important for increasing HCP self-reported competence to use KMT with patients in the future.
Parallel improvements were observed in self-reported shared decision making skills for discussing and/or implementing a ketogenic diet (Table 3). It is important for HCPs to be able to engage patients and families in informed, collaborative treatment discussions, and thus we wanted to provide pilot data in this area as it related to their confidence in implementing discussions of KMT for treating mental health disorders. Preparing HCPs to have the skills and confidence to work with their patients is essential. Previous work has demonstrated that individuals initiating KMT require time to develop an understanding of carbohydrate content in foods, how these foods influence blood glucose and ketone levels, and how to successfully achieve and maintain nutritional ketosis (85). This initial learning period highlights that the complexities of KMT are not immediately intuitive, and a training model like LI-LI may help to provide skills necessary for HCPs to support patients in a collaborative fashion as they navigate KMT. Our inclusion of a shared decision making scale (the DSE) was unique in that most KMT interventions are aimed at families and patients, but less so on the clinician’s ability to engage in this important treatment aspect (86).
Regarding shared decision making, participants identified several important considerations for future patient education and clinical implementation. Experiencing the diet firsthand increased awareness of common adherence barriers and reinforced the importance of proactively discussing strategies to support long-term adherence with patients. Many participants reported feeling confident in explaining KMT. However, they also recognized the value of involving an RDN, and the need to do so when the intervention extends beyond their professional scope of practice. The thematic findings also reinforce that successful implementation requires presenting a balanced perspective that communicates both the potential benefits and practical challenges of KMT, enabling patients to develop realistic expectations and facilitating informed, shared decision making. These findings align with previous work on shared decision making (87, 88), conceptualizing shared decision making as an ongoing therapeutic partnership that is strengthened by incorporating the lived experiences and perspectives of both service users and clinicians and by openly addressing barriers and facilitators to treatment implementation. Our findings extend these concepts beyond mental health and to clinician education by suggesting that incorporating lived experience into KMT training may improve clinicians’ communication skills, confidence, and ability to engage patients in collaborative treatment decisions. Future work should focus on developing evidence-based approaches for discussing and implementing KMT with individuals living with severe mental illness, as their clinical, cognitive, and psychosocial needs may require tailored communication and support strategies.
The qualitative analyses also provided insight into pros and cons of the pilot program. Overall, participants reported high satisfaction with both the educational curriculum and the lived-experience component, with many indicating intentions to either implement KMT in practice or refer appropriate patients, suggesting potential downstream clinical impact. Thematic analyses demonstrated that both the didactic coursework and lived-experience diet contributed meaningfully to learning, while weekly group support sessions with dietitians and peers facilitated adherence and fostered a sense of comradery similar to that reported among patients using KMT (89). Participants’ firsthand experience also highlighted practical challenges that are now better understood by both the research team and participating health care professionals. Recommendations for improving the LI-LI program included providing more information about potential side effects, particularly long-term lipid effects, streamlining and updating the educational modules, and more clearly defining the roles of different health care professionals in implementing KMT versus educating and referring patients to physicians or registered dietitians.
Limitations and future directions
The self-reported competence and shared decision making measures do not equate to objective or applied skills or to behavioral changes associated with implementation. Future testing of an updated training model should include objective implementation outcomes, such as measuring frequency of discussions of KMT, patient education, referrals to registered dietitians and metabolic psychiatry services, and prescription/implementation of KMT when clinically appropriate.
The current study design was a small single arm trial in which several study team members were also study participants. Further, it is important to mention that a smaller sample (N = 26) elected to try the diet phase out of the N = 40 who completed the education. Therefore, not everyone participated in experiential learning. Data from study team members were included in all analyses. Due to the small sample size, sensitivity analyses excluding study team participants were not performed. Author SLM analyzed the data, and the research coordinator recruited participants and collected the data. Therefore, due to several members of the study team participating as subjects, this study is not free from bias, and results should be interpreted with caution, including the magnitude of the effect sizes.
Given also that the diet phase of the study was optional, the diet sample was self-selected and is prone to selection bias, likely towards those with special interest in, or positive inclination towards, KMT. Therefore, findings in the diet phase should be interpreted as exploratory. Furthermore, these study results do not suggest the education course used is exclusive, as other courses on the topic are available. Data and feedback from this study will be used to inform an updated approach to providing KMT education specifically designed for health care professionals providing care to psychiatric patients.
Importantly, the diagnostic groups for which participants indicated consideration in using KMT merely reflect participants’ reported interest. Each illness listed in Figure 5 has undergone or is undergoing some level of research with KMT; however, evidence for the use of KMT in most of these illnesses is in an early stage far from determining the appropriateness of widespread use.
We recommend that future KMT training models for HCPs, like LI-LI, include an expert in KMT delivery on the team, such as a registered dietitian, and additional access to medical providers for monitoring and side effect management. Also, trained educators and implementation scientists should be included in future projects using and studying an updated version of this educational approach. We also believe the next steps should incorporate objective outcome measures of behavior change and larger participant sample sizes to test the reach and impact of this training approach for HCPs.
Conclusion
The present study was a single-arm, open-label pilot trial training HCPs about KMT as an adjunct treatment for mental illness. As this, to our knowledge, was the first study of its kind, training outcomes were limited to self-reported measures of HCPs' perceived competence to introduce, discuss, and implement KMT with patients and perceived self-efficacy to collaborate with patients through shared decision making about incorporating KMT into a treatment plan. Participants demonstrated statistically significant improvements in both self-reported competence and perceived shared decision making self-efficacy. However, this was a small pilot feasibility study in which several members of the study team also participated, and the findings should therefore be interpreted with caution. Nevertheless, these preliminary quantitative and qualitative findings support further refinement of the training program, evaluation in a larger sample, and inclusion of more objective outcome measures to determine whether an updated version of this model can serve as an effective approach for building HCP capacity to use KMT. Our work reinforces that future implementation of evidence-based treatments requires more than passive knowledge acquisition; it depends on building competence, confidence, and practical skills.
Acknowledgments
We thank the participants across the US for their diligent participation in collecting such detailed data. We thank the Maryland Psychiatric Research Center (MPRC) study team for assistance with study conduct including the study coordinator Matthew Glassman who handled recruitment and data collection and regulatory compliance specialist Ann Marie Kearns. We would like to disclose that Matthew Glassman and Ann Marie Kearns also participated in the education and diet phases of the study. Additionally, we thank the RDNs and nutrition specialist physicians working under Denise Potter at AKT, LLC, and assisting with the participant meetings: Stephanie Criteser, RDN, CSP, Marisa Armeno, MD, PhD, Danielle Eller, MS, RDN, CSP, CDN, Lindsay Krupp, RDN, Emily Samuels, MS, RDN, CSP, LD, and Lenycia Neri, PhD, MSc, RDN, MS.
Funding Statement
The author(s) declared that financial support was received for this work and/or its publication. This study was funded by a grant from the Baszucki Foundation. The Ketone meter and test strips used in this study were purchased from Keto Mojo® at a discounted price for research purposes. The foundation nor the company had any role in the study design, data analysis, manuscript preparation, or publication (project number: PF-2025-007).
Footnotes
Edited by: Mansoo Yu, University of Missouri, United States
Reviewed by: Joy M. Rooney, University of Birmingham, United Kingdom
Riccardo Gurrieri, Sant’Anna School of Advanced Studies, Italy
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by University of Maryland Baltimore Institutional Review Board. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
SM: Writing – original draft, Formal analysis, Data curation, Investigation, Visualization, Writing – review & editing, Validation. DP: Methodology, Writing – review & editing, Resources. YZ-I: Resources, Methodology, Writing – review & editing. SC: Supervision, Methodology, Writing – review & editing. HL: Writing – review & editing, Methodology. DR: Methodology, Writing – review & editing. LR: Methodology, Writing – review & editing. CP: Writing – review & editing, Conceptualization, Supervision, Methodology. DK: Funding acquisition, Resources, Writing – review & editing, Methodology, Conceptualization, Writing – original draft, Investigation, Supervision.
Conflict of interest
DK has served as a consultant for Alkermes and served on an advisory board for Boehringer Ingelheim, Teva and Amani Therapeutics. CP receives royalties for his book, Brain Energy, and owns a healthcare practice, MH², that incorporates ketogenic therapies into mental health care. DP is the owner of Advanced Ketogenic Therapies AKT, LLC and co-owner of Keto Mastery Courses, serves on the advisory board for Accord Mental Health, Keto Hope Foundation and Ajinomoto Cambrooke, is a consultant to the Charlie Foundation for Ketogenic Therapies, is on the finance committee for the International Neurological Ketogenic Society and is a research consultant for Mass General Brigham, University of MD, UCSD, UCLA and the Children’s Mental Health Resource Center. In accordance with the Institutional Review Board IRB-approved protocol and methods, authors DK, SM, DR, and LR were participants in the education and dietary intervention; however all data is aggregate and no identifying information is disclosed.
The remaining author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpsyt.2026.1913325/full#supplementary-material
References
- 1. World Health Organization . Over a billion people living with mental health conditions – services require urgent scale-up. (2025). [Google Scholar]
- 2. Krasa HB, Baumgardner JR, Brewer IP, Chou JW, Flottemesch T, Markowitz JT, et al. National and state societal costs of schizophrenia in the US in 2024. JAMA Psychiatry. (2026) 83:341–52. doi: 10.1001/jamapsychiatry.2025.4383 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Muench J, Hamer AM. Adverse effects of antipsychotic medications. Am Fam Phys. (2010) 81:617–22. [PubMed] [Google Scholar]
- 4. Sabé M, Pallis K, Solmi M, Crippa A, Sentissi O, Kaiser S. Comparative effects of 11 antipsychotics on weight gain and metabolic function in patients with acute schizophrenia: a dose-response meta-analysis. J Clin Psychiatry. (2023) 84. doi: 10.4088/JCP.22r14490 [DOI] [PubMed] [Google Scholar]
- 5. Leucht S, Priller J, Davis JM. Antipsychotic drugs: a concise review of history, classification, indications, mechanism, efficacy, side effects, dosing, and clinical application. Am J Psychiatry. (2024) 181:865–78. doi: 10.1176/appi.ajp.20240738 [DOI] [PubMed] [Google Scholar]
- 6. Chue P, Lalonde JK. Addressing the unmet needs of patients with persistent negative symptoms of schizophrenia: emerging pharmacological treatment options. Neuropsychiatr Dis Treat. (2014) 10:777–89. doi: 10.2147/ndt.s43404 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Management of Posttraumatic Stress Disorder and Acute Stress Disorder Work Group . Va/Dod Clinical Practice Guideline for Management of Posttraumatic Stress Disorder and Acute Stress Disorder. Washington, DC: U.S. Government Printing Office; (2023). Affairs DoVDefense Do. [Google Scholar]
- 8. Schottenbauer MA, Glass CR, Arnkoff DB, Tendick V, Gray SH. Nonresponse and dropout rates in outcome studies on PTSD: review and methodological considerations. Psychiatry. (2008) 71:134–68. doi: 10.1521/psyc.2008.71.2.134 [DOI] [PubMed] [Google Scholar]
- 9. Williams T, Phillips NJ, Stein DJ, Ipser JC. Pharmacotherapy for post traumatic stress disorder (PTSD). Cochrane Database Syst Rev. (2022) 3:CD002795. doi: 10.1002/14651858.cd002795.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Hamina A, Taipale H, Lieslehto J, Lähteenvuo M, Tanskanen A, Mittendorfer-Rutz E, et al. Comparative effectiveness of antipsychotics in patients with schizophrenia spectrum disorder. JAMA Netw Open. (2024) 7:e2438358. doi: 10.1001/jamanetworkopen.2024.38358 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Cipriani A, Furukawa TA, Salanti G, Chaimani A, Atkinson LZ, Ogawa Y, et al. Comparative efficacy and acceptability of 21 antidepressant drugs for the acute treatment of adults with major depressive disorder: a systematic review and network meta-analysis. Lancet. (2018) 391:1357–66. doi: 10.1176/appi.focus.16407 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Huhn M, Nikolakopoulou A, Schneider-Thoma J, Krause M, Samara M, Peter N, et al. Comparative efficacy and tolerability of 32 oral antipsychotics for the acute treatment of adults with multi-episode schizophrenia: a systematic review and network meta-analysis. Lancet. (2019) 394:939–51. doi: 10.1176/appi.focus.18306 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Ascher-Svanum H, Faries DE, Zhu B, Ernst FR, Swartz MS, Swanson JW. Medication adherence and long-term functional outcomes in the treatment of schizophrenia in usual care. J Clin Psychiatry. (2006) 67:453–60. doi: 10.4088/jcp.v67n0317 [DOI] [PubMed] [Google Scholar]
- 14. Novick D, Haro JM, Suarez D, Perez V, Dittmann RW, Haddad PM. Predictors and clinical consequences of non-adherence with antipsychotic medication in the outpatient treatment of schizophrenia. Psychiatry Res. (2010) 176:109–13. doi: 10.1016/j.psychres.2009.05.004 [DOI] [PubMed] [Google Scholar]
- 15. Mulder R, Singh AB, Hamilton A, Das P, Outhred T, Morris G, et al. The limitations of using randomised controlled trials as a basis for developing treatment guidelines. BMJ Ment Health. (2018) 21:4–6. doi: 10.1136/eb-2017-102701 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Yoshida K, Takeuchi H. Dose-dependent effects of antipsychotics on efficacy and adverse effects in schizophrenia. Behav Brain Res. (2021) 402:113098. doi: 10.1016/j.bbr.2020.113098 [DOI] [PubMed] [Google Scholar]
- 17. Correll CU, Solmi M, Veronese N, Bortolato B, Rosson S, Santonastaso P, et al. Prevalence, incidence and mortality from cardiovascular disease in patients with pooled and specific severe mental illness: a large-scale meta-analysis of 3,211,768 patients and 113,383,368 controls. World Psychiatry. (2017) 16:163–80. doi: 10.1002/wps.20420 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. De Hert M, Correll CU, Bobes J, Cetkovich-Bakmas M, Cohen D, Asai I, et al. Physical illness in patients with severe mental disorders. I. Prevalence, impact of medications and disparities in health care. World Psychiatry. (2011) 10:52–77. doi: 10.1002/j.2051-5545.2011.tb00014.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Firth J, Siddiqi N, Koyanagi A, Siskind D, Rosenbaum S, Galletly C, et al. The Lancet Psychiatry Commission: a blueprint for protecting physical health in people with mental illness. Lancet Psychiatry. (2019) 6:675–712. doi: 10.1016/s2215-0366(19)30132-4 [DOI] [PubMed] [Google Scholar]
- 20. Nousen EK, Franco JG, Sullivan EL. Unraveling the mechanisms responsible for the comorbidity between metabolic syndrome and mental health disorders. Neuroendocrinology. (2013) 98:254–66. doi: 10.1159/000355632 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Penninx BWJH, Lange SMM. Metabolic syndrome in psychiatric patients: overview, mechanisms, and implications. Dial Clin Neurosci. (2018) 20:63–73. doi: 10.31887/dcns.2018.20.1/bpenninx [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Chan JKN, Correll CU, Wong CSM, Chu RST, Fung VSC, Wong GHS, et al. Life expectancy and years of potential life lost in people with mental disorders: a systematic review and meta-analysis. EClinicalMedicine. (2023) 65:102294. doi: 10.1016/j.eclinm.2023.102294 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Figueroa JF, Phelan J, Orav EJ, Patel V, Jha AK. Association of mental health disorders with health care spending in the Medicare population. JAMA Netw Open. (2020) 3:e201210. doi: 10.1001/jamanetworkopen.2020.1210 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Lipskaya-Velikovsky L, Roe D, Speyer H, Rudnick A, Shields M, Zisman-Ilani Y. Integrating psychiatric rehabilitation into inpatient psychiatric hospitalization to advance personal recovery. Psychiatr Rehabil J. (2026) 49:109–15. doi: 10.1037/prj0000677 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Deegan PE, Stiles A, Rufo M, Zisman-Ilani Y. Awakening on antipsychotic medication: a call to action. Psychiatr Rehabil J. (2024) 47:283–90. doi: 10.1037/prj0000608 [DOI] [PubMed] [Google Scholar]
- 26. Herman PM, Poindexter BL, Witt CM, Eisenberg DM. Are complementary therapies and integrative care cost-effective? A systematic review of economic evaluations. BMJ Open. (2012) 2, 1–16. doi: 10.1136/bmjopen-2012-001046 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. McHugh RK, Whitton SW, Peckham AD, Welge JA, Otto MW. Patient preference for psychological vs pharmacologic treatment of psychiatric disorders: a meta-analytic review. J Clin Psychiatry. (2013) 74:595–602. doi: 10.4088/jcp.12r07757 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. United Nations . Policy brief: COVID-19 and the need for action on mental health. (2020). 1–17. doi: 10.18356/15643913-57-4-6 [DOI] [Google Scholar]
- 29. Patterson EH, Miller C, Hannapel M. Public psychology and holistic approaches to prevention and treatment of depression. Front Psychiatry. (2025) 16:1600094. doi: 10.3389/fpsyt.2025.1600094 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Murray SL, Roche DJO, Palmer CM, Vyas G, Adams HA, Harrington V, et al. International advocacy for ketogenic diet research in schizophrenia: insights from a public petition. Front Public Health. (2026) 14. doi: 10.3389/fpubh.2026.1854868 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Sestan-Pesa M, Horvath TL. Metabolism and mental illness. Trends Mol Med. (2016) 22:174–83. doi: 10.1016/j.molmed.2015.12.003 [DOI] [PubMed] [Google Scholar]
- 32. Sethi S, Berk M, Andreazza AC, Mujica-Parodi LR, Campbell I, Campbell H, et al. Metabolic psychiatry targeting metabolic dysregulation in mental health. Nat Ment Health. (2026) 4:508–20. doi: 10.1038/s44220-026-00609-537880705 [DOI] [Google Scholar]
- 33. Ruan Y, Chen L, She D, Chung Y, Ge L, Han L. Ketogenic diet for epilepsy: an overview of systematic review and meta-analysis. Eur J Clin Nutr. (2022) 76:1234–44. doi: 10.1038/s41430-021-01060-8 [DOI] [PubMed] [Google Scholar]
- 34. Borowicz-Reutt K, Krawczyk M, Czernia J. Ketogenic diet in the treatment of epilepsy. Nutrients. (2024) 16, 1–17. doi: 10.3390/nu16091258 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Sethi S, Wakeham D, Ketter T, Hooshmand F, Bjornstad J, Richards B, et al. Ketogenic diet intervention on metabolic and psychiatric health in bipolar and schizophrenia: a pilot trial. Psychiatry Res. (2024) 335:115866. doi: 10.1016/j.psychres.2024.115866 [DOI] [PubMed] [Google Scholar]
- 36. Abram SV, Kyner JM, Vu A, Naeem Z, Sethi S, Jacob MS, et al. Metabolic improvements with a ketogenic diet correlate with symptom improvement in psychosis: a randomized controlled trial. Schizophr Bull. (2026) 52, 1–11. doi: 10.1093/schbul/sbag082 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Campbell IH, Needham N, Grossi H, Kamenska I, Luz S, Sheehan S, et al. A pilot study of a ketogenic diet in bipolar disorder: clinical, metabolic and magnetic resonance spectroscopy findings. BJPsych Open. (2025) 11:e34. doi: 10.1192/bjo.2024.841 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Chrysafi M, Jacovides C, Papadopoulou SK, Psara E, Vorvolakos T, Antonopoulou M, et al. The potential effects of the ketogenic diet in the prevention and co-treatment of stress, anxiety, depression, schizophrenia, and bipolar disorder: from the basic research to the clinical practice. Nutrients. (2024) 16, 1–22. doi: 10.3390/nu16111546 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39. Janssen-Aguilar R, Vije T, Peera M, Al-Shamali HF, Meshkat S, Lin Q, et al. Ketogenic diets and depression and anxiety: a systematic review and meta-analysis. JAMA Psychiatry. (2026) 83:13–22. doi: 10.1001/jamapsychiatry.2025.3261 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40. Rog J, Wingralek Z, Nowak K, Grudzien M, Grunwald A, Banaszek A, et al. The potential role of the ketogenic diet in serious mental illness: current evidence, safety, and practical advice. J Clin Med. (2024) 13, 1–29. doi: 10.3390/jcm13102819 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Mentzelou M, Dakanalis A, Vasios GK, Gialeli M, Papadopoulou SK, Giaginis C. The relationship of ketogenic diet with neurodegenerative and psychiatric diseases: a scoping review from basic research to clinical practice. Nutrients. (2023) 15, 1–22. doi: 10.3390/nu15102270 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Decker DD, Patel R, Cheavens J, Hayes SM, Whitted W, Lee AJ, et al. A pilot study examining a ketogenic diet as an adjunct therapy in college students with major depressive disorder. Transl Psychiatry. (2025) 15:322. doi: 10.1038/s41398-025-03544-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Longhitano C, Finlay S, Peachey I, Swift JL, Fayet-Moore F, Bartle T, et al. The effects of ketogenic metabolic therapy on mental health and metabolic outcomes in schizophrenia and bipolar disorder: a randomized controlled clinical trial protocol. Front Nutr. (2024) 11:1444483. doi: 10.3389/fnut.2024.1444483 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44. Chen S, Su X, Feng Y, Li R, Liao M, Fan L, et al. Ketogenic diet and multiple health outcomes: an umbrella review of meta-analysis. Nutrients. (2023) 15, 1–19. doi: 10.3390/nu15194161 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45. Athinarayanan SJ, Adams RN, Hallberg SJ, McKenzie AL, Bhanpuri NH, Campbell WW, et al. Long-term effects of a novel continuous remote care intervention including nutritional ketosis for the management of type 2 diabetes: a 2-year non-randomized clinical trial. Front Endocrinol (Lausanne). (2019) 10:348. doi: 10.3389/fendo.2019.00348 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46. McKenzie AL, Athinarayanan SJ, Van Tieghem MR, Volk BM, Roberts CGP, Adams RN, et al. 5-year effects of a novel continuous remote care model with carbohydrate-restricted nutrition therapy including nutritional ketosis in type 2 diabetes: an extension study. Diabetes Res Clin Pract. (2024) 217:111898. doi: 10.1016/j.diabres.2024.111898 [DOI] [PubMed] [Google Scholar]
- 47. Ede G, Bernstein M, Calabrese L, Campbell IH, Laurent N, Palmer CM, et al. Awareness and best practices in using ketogenic therapy to treat serious mental illness: a modified Delphi consensus. Front Nutr. (2026) 13:1749406. doi: 10.3389/fnut.2026.1749406 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48. Kelly DL, Freudenreich O, Sayer MA, Love RC. Addressing barriers to clozapine underutilization: a national effort. Psychiatr Serv. (2018) 69:224–7. doi: 10.1176/appi.ps.201700162 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Bindel LJ, Seifert R. Evidence of lithium underuse in bipolar disorder: analysis of lithium and antipsychotic consumption, prediction of future trends, regional disparities and indicators of rational and inappropriate use in Europe. Naunyn Schmiedebergs Arch Pharmacol. (2025) 398:18049–70. doi: 10.1007/s00210-025-04389-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50. Haddad PM, Correll CU. Long-acting antipsychotics in the treatment of schizophrenia: opportunities and challenges. Expert Opin Pharmacother. (2023) 24:473–93. doi: 10.1080/14656566.2023.2181073 [DOI] [PubMed] [Google Scholar]
- 51. Torrey EF, Lieberman J. The underuse of clozapine and long-acting injectable antipsychotics. Psychiatr Serv. (2025) 76:90–2. doi: 10.1176/appi.ps.20240110 [DOI] [PubMed] [Google Scholar]
- 52. Wang T, Tan JB, Liu XL, Zhao I. Barriers and enablers to implementing clinical practice guidelines in primary care: an overview of systematic reviews. BMJ Open. (2023) 13:e062158. doi: 10.1136/bmjopen-2022-062158 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53. Cook JM, Biyanova T, Coyne JC. Barriers to adoption of new treatments: an internet study of practicing community psychotherapists. Adm Policy Ment Health. (2009) 36:83–90. doi: 10.1007/s10488-008-0198-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54. Cormican A, Hirani SP, McKeown E. Healthcare professionals' perceived barriers and facilitators of implementing clinical practice guidelines for stroke rehabilitation: a systematic review. Clin Rehabil. (2023) 37:701–12. doi: 10.1177/02692155221141036 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55. Forsetlund L, Bjørndal A, Rashidian A, Jamtvedt G, O'Brien MA, Wolf F, et al. Continuing education meetings and workshops: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. (2009) 2009:CD003030. doi: 10.1002/14651858.cd003030.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56. Giguère A, Zomahoun HTV, Carmichael PH, Uwizeye CB, Légaré F, Grimshaw JM, et al. Printed educational materials: effects on professional practice and healthcare outcomes. Cochrane Database Syst Rev. (2020) 8:CD004398. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57. Ivers N, Yogasingam S, Lacroix M, Brown KA, Antony J, Soobiah C, et al. Audit and feedback: effects on professional practice. Cochrane Database Syst Rev. (2026) 6:CD000259. doi: 10.1002/14651858.cd000259.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58. Thomson O'Brien MA, Oxman AD, Davis DA, Haynes RB, Freemantle N, Harvey EL. Educational outreach visits: effects on professional practice and health care outcomes. Cochrane Database Syst Rev. (2000):CD000409. [DOI] [PubMed] [Google Scholar]
- 59. Stetler CB, Damschroder LJ, Helfrich CD, Hagedorn HJ. A guide for applying a revised version of the PARIHS framework for implementation. Implementation Sci. (2011) 6:99. doi: 10.1186/1748-5908-6-99 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60. Cox L, Crump L, Struwing R, Gillum D, Abraham S. Building cultural competence: the lived experience of semester study abroad students. J Christian Nurs. (2017) 34:E35–40. doi: 10.1097/CNJ.0000000000000410 [DOI] [PubMed] [Google Scholar]
- 61. Turner NM, van de Leemput AJ, Draaisma JM, Oosterveld P, ten Cate OT. Validity of the visual analogue scale as an instrument to measure self-efficacy in resuscitation skills. Med Educ. (2008) 42:503–11. doi: 10.1037/t61226-000 [DOI] [PubMed] [Google Scholar]
- 62. Scott JA, Miller GT, Issenberg SB, Brotons AA, Gordon DL, Gordon MS, et al. Skill improvement during emergency response to terrorism training. Prehosp Emerg Care. (2006) 10:507–14. doi: 10.1080/10903120600887072 [DOI] [PubMed] [Google Scholar]
- 63. Bandura A. Self-Efficacy: The Exercise of Control. New York: W.H. Freeman and Company; (1997). [Google Scholar]
- 64. Sockalingam S, Arena A, Serhal E, Mohri L, Alloo J, Crawford A. Building provincial mental health capacity in primary care: an evaluation of a project ECHO mental health program. Acad Psychiatry. (2018) 42:451–7. doi: 10.1007/s40596-017-0735-z [DOI] [PubMed] [Google Scholar]
- 65. Pajares F, Hartley J, Valiante G. Response format in writing self-efficacy assessment: greater discrimination increases prediction. Measurement Eval Couns Dev. (2001) 33:214–21. doi: 10.1080/07481756.2001.1206901237339054 [DOI] [Google Scholar]
- 66. Kelly DL, Hunt J, Vyas G, Glassman M, Brown CH, Fang LJ, et al. A randomized controlled trial of an extension for community healthcare outcomes (ECHO) tele-mentoring program to increase clozapine utilization. Schizophr Bull. (2026) 52, 1–13. doi: 10.1093/schbul/sbaf067 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67. Potter D, Zupec-Kania B. Ketogenic metabolic therapy for psychiatric conditions. In: Keto Mastery (2024). [Google Scholar]
- 68. Cronometer . Science-Backed Nutrition Tracking at Your Fingertips (2026). Available online at: https://cronometer.com/index.html (Accessed August 27, 2026).
- 69. Bandura A. Guide for constructing self-efficacy scales. In: Self-Efficacy Beliefs of Adolescents (Greenwich, CT; Information Age Publishing; ) (2006). p. 307–37. [Google Scholar]
- 70. Kalichman SC, Cain D, Fuhrel A, Eaton L, Di Fonzo K, Ertl T. Assessing medication adherence self-efficacy among low-literacy patients: development of a pictographic visual analogue scale. Health Educ Res. (2005) 20:24–35. doi: 10.1093/her/cyg106 [DOI] [PubMed] [Google Scholar]
- 71. May BA, Limandri BJ. Instrument development of the self‐efficacy scale for abused women. Res Nurs Health. (2004) 27:208–13. doi: 10.1002/nur.20018 [DOI] [PubMed] [Google Scholar]
- 72. O'Connor AM. Decision Self-Efficacy Scale. Ottawa, ON: Ottawa Hospital Research Institute; (1995). [Google Scholar]
- 73. Zisman-Ilani Y, Parker M, Thomas EC, Suarez J, Hurford I, Bowen A, et al. Usability and feasibility of the antipsychotic medication decision aid in a community program for first-episode psychosis. Psychiatr Serv. (2024) 75:807–11. doi: 10.1176/appi.ps.20230230 [DOI] [PubMed] [Google Scholar]
- 74. Zisman-Ilani Y, Roe D, Elwyn G, Kupermintz H, Patya N, Peleg I, et al. Shared decision making for psychiatric rehabilitation services before discharge from psychiatric hospitals. Health Comm. (2019) 34:631–7. doi: 10.1080/10410236.2018.1431018 [DOI] [PubMed] [Google Scholar]
- 75. Braun V, Clarke V. Using thematic analysis in psychology. Qual Res Psychol. (2006) 3:77–101. doi: 10.1191/1478088706qp063oa [DOI] [Google Scholar]
- 76. Ahmed SK, Mohammed RA, Nashwan AJ, Ibrahim RH, Abdalla AQ, Ameen BMM, et al. Using thematic analysis in qualitative research. J Med Surgery Public Health. (2025) 6:100198. doi: 10.2139/ssrn.5222482 [DOI] [Google Scholar]
- 77. Laurent N. From theory to practice: challenges and rewards of implementing ketogenic metabolic therapy in mental health. Front Nutr. (2024) 11:1331181. doi: 10.3389/fnut.2024.1331181 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78. Health Resources and Services Administration Health Workforce . State of the Behavioral Health Workforce, 2025 (2025). Available online at: https://bhw.hrsa.gov/sites/default/files/bureau-health-workforce/data-research/Behavioral-Health-Workforce-Brief-2025.pdf (Accessed August 27, 2026).
- 79. Ballout S. Trauma, mental health workforce shortages, and health equity: a crisis in public health. Int J Environ Res Public Health. (2025) 22, 1–17. doi: 10.3390/ijerph22040620 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80. Kuehn BM. Clinician shortage exacerbates pandemic-fueled "mental health crisis. JAMA. (2022) 327:2179–81. doi: 10.1001/jama.2022.8661 [DOI] [PubMed] [Google Scholar]
- 81. Tilmon SJ, Lee KK, Gower PA, West KSH, Mittal K, Ogle MB, et al. Impact of an urban project ECHO: safety-net clinician self-efficacy across conditions. Am J Prev Med. (2023) 64:535–42. doi: 10.1016/j.amepre.2022.11.004 [DOI] [PubMed] [Google Scholar]
- 82. Gallagher EJ, Liebman M, Bijur PE. Prospective validation of clinically important changes in pain severity measured on a visual analog scale. Ann Emerg Med. (2001) 38:633–8. doi: 10.1067/mem.2001.118863 [DOI] [PubMed] [Google Scholar]
- 83. Raatz M, Ward EC, Moss P, Reilly C, Frederiksen N, Dickinson C, et al. Examining the outcomes of project ECHO((R)) as an interprofessional community of practice for pediatric feeding clinicians. Dysphagia. (2024) 39:208–22. doi: 10.1007/s00455-023-10603-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84. Jensen MP, Chen C, Brugger AM. Interpretation of visual analog scale ratings and change scores: a reanalysis of two clinical trials of postoperative pain. J Pain. (2003) 4:407–16. doi: 10.1016/s1526-5900(03)00716-8 [DOI] [PubMed] [Google Scholar]
- 85. Bellamy EL, Hadjiefthyvoulou F, Walsh J, Brown J, Turner J. Understanding the experiences of ketogenic metabolic therapy for people living with varying levels of depressive symptoms: a thematic analysis. Front Nutr. (2024) 11:1397546. doi: 10.3389/fnut.2024.1397546 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86. Zisman-Ilani Y, Barnett E, Harik J, Pavlo A, O’Connell M. Expanding the concept of shared decision making for mental health: systematic search and scoping review of interventions. Ment Health Rev J. (2017) 22:191–213. doi: 10.1108/mhrj-01-2017-000235579975 [DOI] [Google Scholar]
- 87. Kaminskiy E, Zisman-Ilani Y, Morant N, Ramon S. Barriers and enablers to shared decision making in psychiatric medication management: a qualitative investigation of clinician and service users' views. Front Psychiatry. (2021) 12:678005. doi: 10.3389/fpsyt.2021.678005 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88. Zisman-Ilani Y, Byrne L. Shared decision making and peer support: new directions for research and practice. Psychiatr Serv. (2023) 74:427–8. doi: 10.1176/appi.ps.20220407 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89. Bellamy EL. A retrospective evaluation of an online group ketogenic metabolic therapy intervention on mental health outcomes. Front Nutr. (2026) 13:1751564. doi: 10.3389/fnut.2026.1751564 [DOI] [PMC free article] [PubMed] [Google Scholar]
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Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
