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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05993715
Other study ID # 5951
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 4, 2019
Est. completion date March 1, 2020

Study information

Verified date August 2023
Source Northumbria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to assess if nitrate supplementation influence motor unit (MU) activity following a sustained ischemic contraction and whether this is affected by blood flow restriction (BFR) during the recovery period. Fourteen male participants (mean ± SD, 25 ± 6 years) completed two experimental trials following 5-days of supplementation with either nitrate-rich (NIT) or nitrate-depleted (PLA) beetroot juice in a randomized, double-blinded, cross-over design. Intramuscular electromyography was used to assess MU potential (MUP) size and firing rates (MUFR) during a submaximal (25% MVC) sustained isometric contraction with BFR. These variables were also assessed during a 90 s recovery period with the first half completed with, and the second half completed without, BFR. Nitrate supplementation can expedite the recovery of MUP duration following a sustained ischemic contraction in healthy adults. These novel observations improve understanding of the effects of nitrate on the recovery of neuromuscular function post-exercise and might have implications for recovery of muscle contractile function.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date March 1, 2020
Est. primary completion date February 3, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Male between 18 - 30 years - free from known respiratory insufficiency, cardiovascular disease and neuro-musculo-skeletal problems at present or in the preceding 6 months. - having at least 5 years competitively (team) sport experience. Exclusion Criteria: - having cardiovascular disease, neuromuscular disease and any lower limb injury and treatment for chronic respiratory complaints.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Nitrate supplementation
Participants ingested 2 × 70 mL/day shots of concentrate nitrate-rich (~12.8 mmol/day nitrate) or nitrate-depleted (~0.08 mmol/day nitrite) beetroot juice (Beet It, James White Drinks Ltd., Ipswich, UK). Two shots were supplemented for 5 days; one each morning (~9 am) and one each evening (~9 pm) except for the day of the experimental trial when both shots were taken together 2.5 h before the experimental trial.
Placebo supplementtaion
2 × 70 mL/day shots of concentrate nitrate-depleted (~0.08 mmol/day NO3-) beetroot juice. Two shots were supplemented for 5 days; one each morning (~9 am) and one each evening (~9 pm) except for the day of the experimental trial when both shots were taken together 2.5 h before the experimental trial.

Locations

Country Name City State
United Kingdom Northumbria University Newcastle Upon Tyne

Sponsors (2)

Lead Sponsor Collaborator
Northumbria University Manchester Metropolitan University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma Nitrite Level concentration [nmol] Pre-exercise
Primary Motor Unit Activity Duration (ms), area (uV.ms), firing rate (Hz) Pre-exercise, post-exercise, recovery (45 s)
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