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Effect of Beet-root Juice and PBM Treatments on Muscle Fatigue

Application of Beet-root Juice Supplementation and Photobiomodulation Treatment on Forearm Muscle Fatigue in Older Adults

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05596474
Enrollment
10
Registered
2022-10-27
Start date
2022-09-09
Completion date
2024-08-31
Last updated
2024-03-20

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

Conditions

Health Care Utilization, Healthy Aging

Keywords

Red light therapy, Forearm muscle endurance, Beet-root juice, Electromyography

Brief summary

The goal of this randomized counterbalanced repeated measures study is to test beet-root juice supplementation and red light therapy augment forearm muscle endurance in apparently healthy older adults over 65 years of age. The main questions seek to answer the following question: Does beet-root juice supplementation improve forearm muscle endurance compared to a placebo supplement? Does red light therapy improve forearm muscle endurance compared to a sham light exposure? Does beet-root juice supplementation in combination with red light therapy improve forearm muscle endurance compared to a placebo-sham light control?

Interventions

DIETARY_SUPPLEMENTBeet-root juice

Two days prior to the forearm endurance protocol, participants will be provided and instructed to consume a 400mg nitrate once per day. On the day of the forearm endurance protocol, the participants will be provided and instructed to consume a third 400mg dose of nitrates at least 150 minutes before forearm endurance testing.

RADIATIONred-light therapy

Participants will place their dominant forearm 15 centimeters away from the light source and have their dominant forearm exposed to 660nm wave length light for 10-minutes.

DIETARY_SUPPLEMENTPlacebo

Two days prior to the forearm endurance protocol, participants will be provided and instructed to consume a nitrate depleted placebo once per day. On the day of the forearm endurance protocol, the participants will be provided and instructed to consume a third dose of the nitrate depleted placebo at least 150 minutes before forearm endurance testing.

RADIATIONsham light

Participants will place their dominant forearm 15 centimeters away from the light source and have their dominant forearm exposed to sham light for 10-minutes.

Sponsors

Wake Forest University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Self-reports performing at least 30 minutes of light to moderate intensity physical activity 3 times per week for the last three months

Exclusion criteria

* Currently smoke * Have smoked within the last 6 months * Are taking taking supplements known to increase blood nitrate levels * Have a known kidney disease * Have a known liver disease * Have a known thyroid condition * Have a known gastritis condition * Are taking medications that are known to cause complications with nitrate supplementation * Have known or reported joint pain within the dominant hand

Design outcomes

Primary

MeasureTime frameDescription
Total forearm work performedDuring the forearm exercise fatigue protocol lasting up to 45 minutesWork is the product of the number of times the forearm is activated multiplied by the amount of force produced by the forearm in kilograms.

Secondary

MeasureTime frameDescription
Intermuscular coordinationDuring the forearm exercise fatigue protocol lasting up to 45 minutesSurface electromyography measurements of muscle activity
Forearm enduranceDuring the forearm exercise fatigue protocol lasting up to 45 minutesThe duration of time the participant takes to complete the forearm fatigue protocol

Countries

United States

Contacts

Primary ContactAndrew D Wells, Ph.D.
wellsa@wfu.edu(336) 758-5837

Outcome results

None listed

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