Krupp Center for Integrative Research

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research

Krupp Endowed Fund RFA

Request for Applications for Fiscal Year 2026–27 Funding

Summary

The UC San Diego Krupp Center for Integrative Research (KCIR) Krupp Endowed Fund (KEF) is soliciting applications for funding beginning July 1, 2026. These awards are funded up to $50,000 per year for 1–2 years, up to $100,000 total. Applicants must be responsive to the Primary Aim, Primary Objective, and Research Priorities as described below. KEF studies are typically small, exploratory research projects that generate hypotheses or pilot data needed to design a larger, more definitive study. We also encourage researchers to apply for matching funds from other sources to conduct a larger, more definitive study that builds upon or adds to KEF funding.

For a listing of previously funded KEF projects, visit cih.ucsd.edu/research/studies.

Primary Aim

  • To support research that examines the benefits of natural, complementary and alternative medicine, and integrative medicine approaches that show the greatest promise of bettering human health for the largest number of people, at the lowest cost, without the use of prescription drugs or surgery.

Primary Objective

  • To support innovative clinical research in the fields of diet/nutrition; medicinal food and herbs; homeopathy; and food-derived macro- and micronutrients (which include vitamins and minerals).

Research Priorities

Priority will be given to research projects that meet the Primary Aim and Primary Objective (above), and also:

  1. Promote active involvement of patients in their own care.
  2. Address the health needs and conditions and/or involve the participation of those with limited means.
  3. Utilize inexpensive, readily available, and natural approaches, treatments, and products.
  4. Incorporate a team approach to care (e.g., group-based intervention programs).
  5. Involve Centers for Integrative Health (CIH) patients or those who participate in CIH clinical, nutritional, or educational programs.

Support for Development of Project Ideas

KCIR offers potential applicants the opportunity to discuss and review potential project ideas that prospective applicants may wish to develop for submission. For those who want to submit a concept idea for review, KCIR will advise applicants on potential relevance of proposed project concept ideas as they relate to the objectives of the KEF. Please submit your concept idea for review online.

Award Information

Funds will be disbursed annually. The first year of funding will be allocated upon submission of IRB application. The second year of funding will be released upon approval of an annual progress report. All funds not spent by the end date of the project award may be carried forward pending approval of a no-cost extension. At the end of the project, investigators must return any unexpended funds to the KEF.

Application

A. Eligibility

1. Eligible Applicants

To be eligible to apply for a grant, a potential applicant must be a UC San Diego faculty or staff member and a member of the KCIR. To become a KCIR member, complete the following online survey. UC San Diego faculty or staff who successfully complete the online survey will be automatically granted membership.

2. Eligible Research Projects

Eligible projects will need to meet the following requirements:

  • Focus on diagnosis, prevention, or treatment of common, clinically significant, or costly health conditions (in which introduction of a natural CAM/IM approach could improve clinical outcomes, ameliorate suffering, or reduce costs) without the use of prescription drugs or surgery.
  • Address the use of one or more Complementary, Alternative, or Integrative Medicine (CAM/IM) approaches in the fields of natural diet (may also include lifestyle focus if part of a comprehensive diet and lifestyle program); medicinal foods and herbs; food-derived macro- and micronutrients (which include vitamins and minerals); and homeopathy.
  • Other CAM/IM research projects will be considered on merit after all existing work in the fields above have been exhausted.

The following types of projects are allowed:

  • Self-contained research projects that generate pilot data needed to design a larger, more definitive study.
  • Clinical studies that bring credibility to previous low-level research already done by others.
  • Clinical studies that also employ a basic science component to determine biological mechanisms of CAM/IM approaches (as specified above).
  • Epidemiologic (observational) investigations of effects of CAM/IM use on important health outcomes in specific patient populations.
  • Health services research addressing cost, utilization, or satisfaction with CAM/IM care.

B. Applications will be received in two stages:

  1. Letter of Intent (LOI): reviewed for scientific merit and program relevance. The LOI must include: Principal Investigator and Co-Investigator name(s), title of project, type of study, requested grant type/funding level, core services requested, and 500-word maximum narrative. We suggest writing the abstract in a Word document and then copying/pasting into the online LOI form.
  2. Full application (by invitation only): Each full application must follow a required template that includes:
    • Research plan (4-page limit with the following sections: Specific Aims (1 page), Significance and Innovation (1 page), and Approach (2 pages));
    • Literature cited (no page limit);
    • Budget and budget justification (no page limit);
    • Biosketch(es) of P.I. and key personnel (include other support); and
    • Letter(s) of support (as appropriate).

C. All submissions should adhere to the following format specifications:

  1. 11-point Arial font
  2. Single-spaced
  3. 0.5 inch margins on all sides
  4. 8½″ × 11″ pages
  5. Number all pages
  6. Combine all pages into one document
  7. Microsoft Word or PDF format
  8. At the top of the first page:
    1. Title of proposed study
    2. PI name(s)
    3. Amount of funding requested per year, listed by year
  9. Include the requested KEF core services to be utilized in the study
  10. Name final file as “PILastName_AbbreviatedStudyTitle_FY27”

D. Deadlines, Notices, and Funding Cycle Dates:

  1. Letter of Intent (LOI) Deadline: LOI must be received via electronic submission by 11:59 PM Pacific time, Sunday, Jan. 18, 2026.
  2. Notice of LOI Decisions: By Friday, Feb. 27, 2026.
  3. Full Application Deadline (by invitation only): Full applications must be received via electronic submission by 11:59 PM Pacific Time on Monday, Apr. 27, 2026.
  4. Notice of Awards: ~ By June 2026
  5. Funding Cycle:
    1. Starts FY 2026–27 (Jul. 1, 2026)
    2. Funds allocated upon submission of IRB application (estimated ~ Oct. 1, 2026)

E. Evaluation Criteria

All submissions should be well-written, precise, and succinct. LOIs are scored for eligibility (including alignment with Primary Aim, Primary Objective and Research Priorities), scientific merit (significance of problem, feasibility of project, and confidence in PI/research team), cost efficiency, and programmatic impact.

Full applications (if invited) will be subject to a comprehensive scientific and programmatic review. The following scoring criteria will be used in the Scientific Review to evaluate applications:

  1. Significance. Does the project address an important (clinically significant, costly) health problem or a critical barrier to progress in a field of research?
  2. Innovation. Does the application challenge and seek to shift current research or clinical practice paradigms by utilizing novel theoretical concepts, approaches or methodologies, instrumentation, or interventions?
  3. Approach. Are the overall strategy, methodology, and analyses well-reasoned and appropriate to accomplish the specific aims? Are potential problems, alternative strategies, and benchmarks for success presented? Is the project feasible?
  4. Environment. Will the scientific and clinical environment in which the work will be done contribute to the probability of success?
  5. Investigator(s). Is/are the investigator(s) well suited to the project? If the investigators are in the early stages of their careers, do they have appropriate experience, training and senior mentorship? If established, have they demonstrated an ongoing record of accomplishments that have advanced their field(s)?

Programmatic review criteria include: strategic alignment with KEF aims, objectives and priorities; efficiency and responsibility in use of grant funds; and demonstration of greatest impact to society and future research, if funded. The highest scoring applications will be presented to a funding committee who makes the final decisions.

F. Core Services

Study efficiency is an important factor in our consideration. In order to reduce the cost of all of our grants, depending on availability, the KCIR may be able to provide selected core research services such as:

  • Consulting on CAM/IM modalities
  • Access to specific CAM/IM practitioners
  • Access to specific patient groups
  • Access to healthy volunteers
  • Research design and grant application development
  • Support in consent form development/IRB application and correspondence
  • Questionnaire selection and design
  • Dietary counseling / intervention
  • Nutrition / anthropometric / behavioral assessment
  • Database development / management
  • Statistical support
  • Manuscript preparation

We strongly recommend that potential applicants contact KCIR to discuss availability of services and their customization in support of your project's success and cost-effectiveness: KruppREC@ucsd.edu.

G. Presentations and Publications

Awardees are expected to publish their findings in scholarly peer-reviewed journals and present their research at professional meetings. All publications, grants, and presentations resulting from research funded by the KEF must cite the UC San Diego Krupp Center for Integrative Research as the funding agency and indicate the grant title and number. If a project is required to be registered at ClinicalTrials.gov, the Principal Investigator is responsible for doing so before beginning the research.

H. Progress Reports

All investigators selected for funding will be required to submit a bi-annual progress report. This report will consist of a detailed description of progress to date, which includes: IRB approval and any amendment date(s), subject recruitment and enrollment, adverse events, milestones, study modifications, a budget update, and a listing of all submitted publications and grant applications (pending or funded), meeting abstracts, and seminars relating to the project. We now request that all progress reports be submitted online through our website.

The Effect of Anti-Inflammatory Diet on Clinical and Biologic Outcomes in Long-COVID (PASC) Patients

This study aimed to assess the feasibility of a 12-week anti-inflammatory diet (ITIS) among Long-COVID (PASC) patients. This study also explored diet-induced changes in clinical symptoms and plasma inflammatory marker levels. The intervention included individualized dietary counseling and 2 weeks of a Long-COVID ITIS diet plan including a food basket of key ingredients, recipes, and manuals to learn how to follow an anti-inflammatory diet.

Study findings and publications can be found under the Outcomes section of this website.

Principal Investigator(s)
Email
krupp-wellness@health.ucsd.edu
Primary Center

Glutathione Support for Health: A Randomized Trial

This randomized, placebo-controlled study aimed to determine the feasibility and potential effects on glutathione status using a Whole-Food Plant-Based (WFPB) diet among an adult population with type-2 diabetes. The intervention group included educational classes and meal-planning recommendations aiming to increase the intake of glutathione-rich foods. 

Principal Investigator(s)
Email
krupp-wellness@health.ucsd.edu
Primary Center

Clinical and Biological Changes in Rheumatoid Arthritis Patients Exposed to an Anti-inflammatory Diet

This pilot study investigated how a short-term anti-inflammatory dietary intervention might reduce pain and inflammation in individuals with rheumatoid arthritis (RA). Over a two-week period, participants followed a specialized diet (ITIS) rich in omega-3 fats, antioxidants, and anti-inflammatory ingredients like turmeric, while avoiding pro-inflammatory foods such as red meat, gluten, nightshades, and lactose. Researchers observed improvements in joint tenderness, swelling, and overall disease activity, suggesting dietary changes may complement standard RA treatments.

Study findings and publications may be found under the Outcomes section of this website.

Principal Investigator(s)
Email
krupp-wellness@health.ucsd.edu
Primary Center

Clinical, Inflammatory, and Microbiome Effects of Dietary Modification in Women With Endometriosis

This study aimed to determine whether increasing consumption of a Whole-Food Plant-Based (WFPB) diet can improve gut microbiome diversity, quality of life, pain, and inflammation in women with endometriosis. Study outcomes were measured before and after a 3-month intervention, including dietary counseling, online cooking classes, and individual and group health coach sessions. Study findings and publications can be found under the Outcomes section of this website.

Principal Investigator(s)

Sanjay Agarwal, MD 

Rob Knight, PhD
Lauren Foster, PhD
Gordon Saxe, MD, PhD 

Primary Center

Effects of Cannabidiol (CBD) Versus Placebo as an Adjunct to Antipsychotics in Early Psychosis

This 6-week double-blinded trial examines whether individuals in the early stages of psychosis (EP) respond to 1000 mg of endocannabinoids (CBD) with the aim of improving positive, negative, and cognitive symptoms of psychosis. Researchers are exploring the possibility that CBD might reduce anxiety, and perhaps normalize biological stress response. Symptoms, eating behaviors, metabolic parameters, cannabinoid, and biomarkers of inflammation and cortisol are measured at baseline, 3 weeks and end of study in a population with a diagnosis of first episode psychosis who are stabilized on antipsychotic medication.

Principal Investigator(s)

Kristin Cadenhead, MD

Heline Mirzakhanian, Ph.D
Cris Achim, MD, Ph.D  

Email
krupp-wellness@health.ucsd.edu
Primary Center

Aromatherapy and Healing Visual Art for Hospitalized Cancer Patients

The study aimed to evaluate the feasibility and explore the potential effects of using aromatherapy and visual mindfulness as complementary therapies to address pain and nausea in hospitalized cancer patients. Aromatherapy involves olfactory stimulation of selected scents via a patch, and visual mindfulness involves watching curated videos by cinematographer Louie Schwartzberg.

Principal Investigator(s)

Jay Varughese, MD

Alice Chen, DO

Primary Center

Mushrooms as COVID-19 Vaccine Adjunct

A randomized, double-blinded, placebo-controlled clinical trial to evaluate the safety of FoTv (a combination of two polypore mushrooms, Fomitopsis officinalis, and Trametes versicolor) in an adult population at the time of COVID-19 vaccination. Researchers examined the effect of FoTv vs. placebo for use as an adjunct to vaccination for COVID-19. Vaccine-related side effects following COVID-19 vaccination were examined in both study groups.  

Study-related publication(s) may be found in the Outcomes section of this website. 

Principal Investigator(s)
Email
krupp-wellness@health.ucsd.edu
Primary Center

Randomized Controlled Trial (RCT) of Immune Supporting Mushrooms for COVID-19

A multi-centered, randomized, double-blinded, placebo-controlled clinical trial to evaluate the safety of FoTv (a combination of two polypore mushrooms, Fomitopsis officinalis and Trametes versicolor) for COVID-positive outpatients with mild-to-moderate symptoms. Researchers used changes in COVID-19 viral load, blood markers, and a 14-day symptom diary to examine the safety, feasibility, and preliminary effects of the study product versus placebo. Study findings and publications may be found under the Outcomes section of this website.


 

Principal Investigator(s)
Email
krupp-wellness@health.ucsd.edu
Primary Center