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Beetroot Juice Resistance Training Older Adults

Effect of Beetroot Juice on Body Composition, Physical Function, Muscle Strength, and Peak Oxygen Consumption in Resistance Trained Older Adults Consuming a Protein Supplement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05460351
Enrollment
24
Registered
2022-07-15
Start date
2014-02-28
Completion date
2015-05-31
Last updated
2022-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Old Age; Atrophy, Sarcopenia

Brief summary

The present study compared the effects of a nitrate containing beetroot juice supplement (BRJ+Nitrate) vs. a placebo (Control) on total and regional fat free mass, quadriceps muscle strength, lower body mobility, and VO2peak in healthy, older adults undergoing a 10-week long progressive resistance training program with protein supplementation.

Interventions

DIETARY_SUPPLEMENTBRJ+Nitrate

Participants in this group drank a 70 mL bottle of Beet It Sport drink with nitrate plus 15 grams of whey protein 3 days a week following a resistance exercise training program

DIETARY_SUPPLEMENTControl

Participants in this group drank a 70 mL bottle of Beet It Sport drink without nitrate plus 15 grams of whey protein 3 days a week following a resistance exercise training program

Sponsors

Wake Forest University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

A third party not involved with the conduct of the study provided research staff with the beetroot juice in participant specific coded bottles. The research staff then distributed these coded bottles to the participant. At the end of the trial, the code was revealed for intervention assignment.

Intervention model description

Participants will be randomized into one of two groups. The first group will consume daily beetroot juice containing 380 mg of nitrate and the second group will consume daily beetroot juice with nitrate removed. Both groups will undergo resistance exercise training and consume a protein supplement

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Able to provide own transportation to study testing visits and intervention * Able to read and write in English * Nondiabetic, i.e. fasting glucose \< 126 mg/dl * Sedentary (less than 60 minutes of moderate intensity structured physical activity each week and occurs in no more than 10 minute blocks and not participating in a resistance exercise training program) * Willingness to provide informed consent and participate in intervention. Participants with diagnosed depression were permitted to participate provided that they have been medically stable without medication change for at least 3 months.

Exclusion criteria

* Smoking or use of chewing tobacco * Involved in another intervention research study * Diabetic (type 1 or 2) * Atrophic gastritis * Hypo- or hyperthyroidism * Gout or history of kidney stones * History of hypotension * Premenopausal (women) * Aversion to study-related testing procedures * Allergy/sensitivity/aversion to beetroot beverages or protein supplement * Medical conditions with contraindications for engaging in resistance training program or taking the protein supplement * Systemic, uncontrolled diseases (diabetes, recent (last 6 months) or current treatment of cancer, thyroid disorders, cardiovascular disease, COPD, or inflammatory bowel diseases) * Use of any of the following medications: phosphodiesterase type 5 inhibitors, nitroglycerin or nitrate preparations, proton pump inhibitors, or medications for hypothyroidism * Potential inability to complete the tasks required for the protocol as well as conditions that may interfere with interpretation of results including: inability to ambulate, severe congestive heart failure or severe cardiovascular disease, neoplasm for practical and neurophysiologic reasons * Individuals with contraindications for performing a graded exercise test or have medical contraindications for participating in a scheduled exercise training program * Individuals more than 300 pounds or less than 125 pounds due to DEXA weight limits and possibility of exceeding recommended daily nitrate dose of 7 mg/kg body weight, respectively.

Design outcomes

Primary

MeasureTime frameDescription
Whole body fat free massCollected at baselineMass of fat free tissue
Whole body fat massCollected at baselineMass of fat tissue
Thigh muscleCollected at baselineVolume of thigh muscle
Thigh intermuscular fatCollected at baselineVolume of fat in the thigh muscle
Thigh subcutaneous fatCollected at baselineVolume of subcutaneous fat in the thigh
Visceral fatCollected at baselineVolume of visceral fat
Muscle strengthCollected at baselineStrength of quadriceps muscle at a speed of 60 degrees per second
400 meter walkCollected at baselineTime to walk 400 meters
Stair climb timeCollected at baselineTime to ascend and descend 12 stairs
Peak oxygen consumptionCollected at baselinePeak oxygen consumed at maximal exercise during graded exercise testing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026