Effects of a Very Low Carbohydrate Ketogenic Diet or Mediterranean Diet on Markers of Musculoskeletal Health in Older Adults

NCT ID: NCT06203392

Last Updated: 2026-01-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-07-15
• Study Completion Date: 2025-11-24

Brief Summary

Preclinical data indicate that very low carbohydrate ketogenic diets (KD) may prevent progression of age-related sarcopenia (skeletal muscle decline) but also may disturb bone metabolism. The investigators will pilot test a randomized trial comparing the effects of short-term adaptation to a well-formulated ketogenic diet and Mediterranean diet on markers of bone metabolism and muscle function in older adults. The expected results will help inform the benefit-risk assessment for older patients considering longer term use of KD therapy.

Detailed Description

Eucaloric very low carbohydrate ketogenic diets (KD) are therapeutic diets that mimic fasting by generating ketones for metabolic fuel while meeting nutritional requirements (nutritional ketosis). Nutritional ketosis may broadly benefit healthspan through mechanisms such as suppression of inflammation or induction of autophagy, and preclinical and emerging clinical data indicate that KD therapy may help slow progression of age-related conditions including sarcopenia. However, questions remain about the benefits and risks of KD, especially relative to recommended therapeutic diets such as the Mediterranean Diet (MD) for which there is evidence of benefit for age-related conditions. For example, KD has shown efficacy for weight loss, which could reduce ectopic lipid accumulation that weakens muscle and bone. KD has been shown to increase skeletal muscle mitochondrial mass, mitochondrial activity, and strength in aged mice, possibly by increasing peroxisome proliferator-activated receptor activity and preserving fast-oxidative fibers that typically decline with age. However, long term use of KD may adversely impact bone. KD can cause deterioration of bone in juvenile mice without evidence of undernutrition and is associated with skeletal demineralization in children being treated for drug-resistant epilepsy.

Given the burden of musculoskeletal disease in older Americans, it is vital to understand the effects of KD on the musculoskeletal system of older adults to inform the benefit-risk assessment for an older patient and to optimize the effectiveness of KD for age-related conditions. The investigators are conducting a pilot test of a randomized clinical trial comparing the effects of short-term adaptation to a well-formulated KD and MD on markers of bone health and muscle function in older adults. The investigators will supply fresh prepared meals to achieve high adherence to the dietary interventions and adequate contrast in metabolic state between treatment groups.

Potential participants will complete a screening process so the investigators can determine whether potential participants are eligible to enroll in the study. At the first screening visit, the study team will measure blood pressure, height, and weight. Individuals will complete questionnaires that collect information about their health history, dietary intake, and physical activity habits. No more than 50 mL of blood will be collected from potential participants to run routine clinical lab tests to evaluate health status.

If an individual remains eligible after the first screening visit, they will be invited to complete a 24-hour urine collection (at home) and to schedule a second screening visit. At the second screening visit, a physician will conduct a physical exam and assess their body composition with an x-ray technology called dual-energy x-ray absorptiometry (DEXA or DXA).

If an individual remains eligible after the second screening visit, they will be invited to enroll in the dietary intervention study. Once enrolled, the participant will be assigned to either a very low carbohydrate ketogenic dietary pattern or a Mediterranean dietary pattern. The investigators will provide most of the food the participant will need each day in the form of a nutrition shake (breakfast) and two prepared meals (lunch and dinner). A study dietitian will be available to provide continuous support through a secure messaging app.

While in the dietary intervention phase of the study, participants will come to the UF Clinical and Translational Science Building once a week for 6 weeks. The study team will measure participant blood pressure and weight at each visit. At the first, middle, and final visits, the study team will collect a blood sample and urine sample from participants for lab testing, and participants will complete a short series of tests that measure physical performance.

Our ultimate research goal is to determine the effects of KD on body composition and clinically relevant measures of bone health and muscle function, as those data are needed to (1) inform the benefit-risk assessment for an older patient who is considering longer term adherence to KD therapy and (2) optimize the effectiveness of KD for age-related conditions.

Conditions

Aging; Musculoskeletal Diseases

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

Very low carbohydrate ketogenic diet for six weeks

Group Type: EXPERIMENTAL

Very low carbohydrate ketogenic diet

Intervention Type: OTHER

Very low carbohydrate ketogenic diet provided for six weeks

Mediterranean diet for six weeks

Group Type: ACTIVE_COMPARATOR

Mediterranean diet

Intervention Type: OTHER

Mediterranean diet provided for six weeks

Interventions

Very low carbohydrate ketogenic diet

Very low carbohydrate ketogenic diet provided for six weeks

Intervention Type: OTHER

Mediterranean diet

Mediterranean diet provided for six weeks

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Postmenopausal
• BMI 20 to <40 kg/m2
• Weight stable for last 12 months
• Male or female biological sex
• Willing to eat supplied food and adhere to dietary advice
• Willing to document food intake
• Willing to maintain weight
• Willing to attend study visits
• Smartphone ownership
• Community-dwelling with permanent living arrangement
• Resides within 30 miles of Gainesville, FL
• Willing to avoid alcohol intake
• Estimated energy requirement ≤ 2,700 kcal/day
• Have a refrigerator and means to reheat food within dwelling
• Bone mineral density tested within past 5 years or U.S. ethnicity-specific fracture risk assessment tool (FRAX) indicates ten year-probability of hip fracture <3% and ten year-probability of major osteoporotic fracture <20%

Exclusion Criteria

• Pre- or peri-menopausal
• Fracture in past 6 months
• Circulating 25-hydroxyvitamin D < 20 ng/mL at screening
• History or prevalence of metabolic bone disease
• Chronic kidney disease diagnosis or eGFR <60 mL/min/1.73 m2 at screening
• Current or history of cancer excluding non-melanoma skin cancer
• Clinical cardiovascular disease, excluding current use of anti-hypertensive medication
• LDL cholesterol at screening that is elevated (≥ 160 mg/dL) or uncontrolled (≥ 100 mg/dL despise current statin treatment)
• History of recurrent kidney stones
• Current diabetes diagnosis
• Liver disease
• Pancreatic disease
• Heavy drinking per CDC definition
• Currently smoke tobacco
• Malabsorption disease including celiac and inflammatory bowel disease
• Inborn error of metabolism including disorders of fatty acid transport or oxidation, organic aciduria, porphyria, or familial hyperlipidemia
• Dementia diagnosis
• Dietary restrictions including food allergy, vegetarianism, veganism or gluten, dairy, or seafood avoidance
• Current or history of diagnosed eating disorder
• Thyroid disorder
• Male hypogonadism
• Menopause before age 40 years
• Gender-affirming hormone therapy
• Currently eat a ketogenic or Mediterranean diet based on ASA 24-hour dietary recall and Mediterranean diet screener
• Participation in concurrent research study
• Currently homeless
• Presence or possibility of co-morbid condition discovered during medical screening that would elicit safety concerns
• Living in skilled nursing facility
• Current gallbladder disease including gallstones
• History of 2 or more abdominal surgeries
• Current chronic constipation
• Current chronic diarrhea

• Minimum Eligible Age: 55 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute on Aging (NIA)

NIH

Sponsor Role: collaborator

University of Florida

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Cora Best, PhD, RDN

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

University of Florida

Gainesville, Florida, United States

Countries

United States

Other Identifiers

2P30AG028740-16

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IRB202301329

Identifier Type: -

Identifier Source: org_study_id