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Study to Examine the Effects of ATP Supplementation on Muscle Excitability and Reaction Time During and Following a Repeated Sprint Bout

Study to Examine the Effects of ATP Supplementation on Muscle Excitability and Reaction Time During and Following a Repeated Sprint Bout

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02093611
Enrollment
42
Registered
2014-03-21
Start date
2013-07-31
Completion date
2015-08-31
Last updated
2015-09-28

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

Conditions

Muscle Fatigue Caused by Repetitive Muscle Exercise

Brief summary

We hypothesize that adenosine-5'-triphosphate (ATP) supplementation will be able to enhance motor unit recruitment while simultaneously blunting the decline in power and reaction time that is typically seen during repetitive sprints. This will give researchers a better understanding of the mechanism by which ATP supplementation can augment power, especially under high fatiguing conditions.

Detailed description

Healthy participants of similar training status as previously tested will be enrolled into the study. The participants will be randomly assigned to either placebo supplementation or to 400 mg ATP per day for 14 days. The supplements will be taken in the morning and the last dose will be taken 30 min prior to testing on the last day. Testing will be performed at baseline and after the 14 days of supplementation. Ten successive sprints will be conducted on the Wingate apparatus as this has been previously demonstrated to decrease muscle excitability. After the sprints, muscle excitability, reaction time, and vertical jump power will be measured. In addition a blood sample will be obtained before and after supplementation and complete blood hematology and chemistry analyses will be performed. It is expected that ATP supplementation may help maintain muscle excitability and power after the successive sprint sessions.

Interventions

DIETARY_SUPPLEMENTPlacebo
DIETARY_SUPPLEMENTATP

400 mg of ATP

Sponsors

University of Tampa
CollaboratorOTHER
Metabolic Technologies Inc.
Lead SponsorINDUSTRY

Study design

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

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Agree to eating a diet approved by a registered dietician consisting of the following by caloric percentages: 15-20% protein, 44-55% carbohydrate, and 25-30% fat. * Must not have taken performance enhancing supplements for at least 3 months prior to the study start, * Must be a non-smoker. * Must not be taking amino acid supplements. * Must not be using anabolic or catabolic hormones. * Must not be taking any medications known to influence variables to be measured in the study.

Exclusion criteria

* Will not agree to eating a diet approved by a registered dietician consisting of the following by caloric percentages: 15-20% protein, 44-55% carbohydrate, and 25-30% fat. * Has taken performance enhancing supplements for at least 3 months prior to the study start, * Is currently a non-smoker. * Is currently taking amino acid supplements. * Is currently using anabolic or catabolic hormones. * Is currently taking medications known to influence variables to be measured in the study.

Design outcomes

Primary

MeasureTime frameDescription
Muscle ExcitabilityDay 14Muscle excitability will be measured using Delsys Wireless Electromyography (EMG) sensors.

Secondary

MeasureTime frameDescription
PowerDay 14Muscle power will be measured using the Wingate and vertical jump power measures.

Other

MeasureTime frameDescription
Reaction TimeDay 14Reaction time will be measured using a Dynavision apparatus.
Blood Biochemical AnalysesDay 14Blood chemistries and hematology will be measured after the 14 days of supplementation.

Countries

United States

Outcome results

None listed

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