ClinicalTrials.gg
Status unknownNCT05313490Updated Aug 24, 2022

Exercise Fatiguability in Older Adults: The Protective Effects of Dietary Nitrate Supplementation

An interventional study of Beetroot Juice and Placebo Beetroot Juice in Aging, sponsored by Marquette University. Status unknown at 1 site in United States. Open to participants aged 60 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-08-24.

Sponsored by Marquette University · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Aug 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
60 Years to 90 Years
Sex
All
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Study summary

Vascular and skeletal muscle function decline with age and are associated with decreased nitric oxide (NO) bioavailability. Dietary nitrate supplementation in the form of beet root juice increases NO bioavailability and improves exercise tolerance in younger adults, yet its effects on fatigability in older adults are largely unknown. The proposed research will investigate the impact of increased NO bioavailability on vascular function, skeletal muscle bioenergetics, and fatigability in older (≥65 yrs) men and women.

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Conditions studied

  • Aging
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In context

Lead sponsor

Marquette University is the lead sponsor of 38 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
60 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy men and women ≥ 60 years old

Exclusion criteria

Exclusion Criteria:

  1. body mass index ≥40 kg/m2;
  2. type 1 or type 2 diabetes or HbA1c >6.5%
  3. uncontrolled hypertension;
  4. active cancer, cancer in remission, or having received treatment for any form of cancer in the previous five years;
  5. coronary artery disease;
  6. cardiovascular disease (e.g., PAD, PVD);
  7. abnormal and untreated thyroid function;
  8. chronic and/or regular nonsteroidal anti-inflammatory drugs (NSAID) consumption,
  9. tobacco use (includes smoking);
  10. any condition that presents a limitation to exercise (e.g., severe arthritis, COPD, neuromuscular disorder, moderate or severe cognitive impairment, Alzheimer's Disease, severe untreated sleep apnea).
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    Beetroot Juice

    The subject will ingest 140mL of a nitrate-rich beetroot juice each day for 7 consecutive days.

    Dietary Supplement: Beetroot Juice

  • Placebo comparator
    Placebo Beetroot Juice

    The subject will ingest 140mL of a placebo (nitrate-depleted) beetroot juice each day for 7 consecutive days.

    Other: Placebo Beetroot Juice

Interventions

  • Dietary supplementBeetroot Juice

    7 days of 140 mL per day of beetroot juice

    Also known as: James White Drinks Beet It Sport 400

  • OtherPlacebo Beetroot Juice

    7 days of 140 mL per day of placebo beetroot juice

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What researchers measure

Primary outcomes

  1. Change in fatigability of the knee extensor muscles with beetroot juice supplementation

    Fatigability will be quantified as the reduction in limb muscle power output during a 4-minute dynamic fatiguing exercise task using a dynamometer. Fatigability after 7 days of beetroot juice supplementation will be compared with fatigability after 7 days of placebo supplementation, with the outcome measure being the change (or difference) between these two supplementation conditions.

    Time frame: Day 8 (after 7 days of placebo supplementation) and day 29 (after 14 days of a washout period with no supplementation plus 7 days of beetroot juice supplementation)

Secondary outcomes

  1. Change in femoral artery blood flow with beetroot juice supplementation

    Femoral artery blood flow will be quantified as the change in femoral artery blood flow during a 4-minute dynamic fatiguing exercise task using a ultrasonography. Femoral artery blood flow after 7 days of beetroot juice supplementation will be compared with Femoral artery blood flow after 7 days of placebo supplementation, with the outcome measure being the change (or difference) between these two supplementation conditions.

    Time frame: Day 8 (after 7 days of placebo supplementation) and day 29 (after 14 days of a washout period with no supplementation plus 7 days of beetroot juice supplementation)

  2. Change in muscle efficiency with beetroot juice supplementation

    Muscle efficiency will be quantified as the ATP cost of contraction using phosphorus magnetic resonance spectroscopy (P-MRS). Muscle efficiency after 7 days of beetroot juice supplementation will be compared with muscle efficiency after 7 days of placebo supplementation, with the outcome measure being the change (or difference) between these two supplementation conditions.

    Time frame: Day 8 (after 7 days of placebo supplementation) and day 29 (after 14 days of a washout period with no supplementation plus 7 days of beetroot juice supplementation)

Other outcomes

  1. Change in plasma nitrate concentration with beetroot juice supplementation

    Plasma nitrate concentration will be quantified using a nitrate colorimetric assay. Plasma nitrate concentration after 7 days of beetroot juice supplementation will be compared with plasma nitrate concentration after 7 days of placebo supplementation, with the outcome measure being the change (or difference) between these two supplementation conditions.

    Time frame: Day 8 (after 7 days of placebo supplementation) and day 29 (after 14 days of a washout period with no supplementation plus 7 days of beetroot juice supplementation)

  2. Change in plasma nitrite concentration with beetroot juice supplementation

    Plasma nitrite concentration will be quantified using a nitrite colorimetric assay. Plasma nitrite concentration after 7 days of beetroot juice supplementation will be compared with plasma nitrite concentration after 7 days of placebo supplementation, with the outcome measure being the change (or difference) between these two supplementation conditions.

    Time frame: Day 8 (after 7 days of placebo supplementation) and day 29 (after 14 days of a washout period with no supplementation plus 7 days of beetroot juice supplementation)

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Study locations

1 of 1 sites recruiting
  • Marquette University
    Milwaukee, Wisconsin 53233, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 24, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05313490
Lead sponsor
Marquette University
Responsible party
Timothy Fulton (Principal Investigator, Marquette University) — Principal investigator
First posted
Apr 6, 2022
Start date
May 1, 2022
Primary completion
Dec 31, 2023 (estimated)
Completion
Dec 31, 2023 (estimated)
Last update
Aug 24, 2022

Study contacts

Timothy Fulton, PhD
Contact
timothy.fulton@marquette.edu
319-290-5529

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Beet juice

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