Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04292106
Other study ID # 092619
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 26, 2019
Est. completion date March 30, 2020

Study information

Verified date January 2022
Source Lipscomb University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Red Spinach is a natural food which is a rich source of nitrates, which are beneficial in hemodynamics, cardiovascular function, and have natural hypotensive and antianginal effects. Red spinach extract has been shown to be beneficial in exercise performance, albeit mostly in aerobic exercise. In a previous study in our lab, we found that dietary nitrate consumption resulted in significantly greater isometric force production in teenage males. However, currently there is little know regarding the effects of dietary nitrate supplementation on isometric strength, resistance exercise and cognitive performance.


Description:

This research study is designed to measure the effects of red spinach extract (RSE) on markers of physical and cognitive performance during and following anaerobic exercise.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date March 30, 2020
Est. primary completion date March 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 34 Years
Eligibility Inclusion Criteria: - 18-34 years old Participants must have at least 1 year of resistance training experience. - Free of any physical limitations, medications, and supplements that may affect performance, as determined by a health and activity questionnaire. - Are free of musculoskeletal injuries - Are not taking medications that may interfere with study measurements Exclusion Criteria: - Participants that cannot take either the RSE or placebo supplement will be excluded, as this will be a double-blind study. - Furthermore, participants that cannot participate in pre- and post-research testing, and/or those that cannot commit to regular training sessions will be excluded. - Inability to perform physical exercise (determined by health and activity questionnaire) - Taking any other nutritional supplement or performance enhancing drug. - Any chronic illness that causes continuous medical care

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Red Spinach Extract (RSE)
Oral capsules containing 2g of Red Spinach Extract will be consumed daily for 7 days
Placebo
Oral placebo capsules will be taken consisting of maltodrextrin daily for 7 days

Locations

Country Name City State
United States Jeremy Townsend Nashville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Lipscomb University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bench Press Repetitions to Fatiuge Number of repetitions completed in each set during the acute exercise bout will be recorded and analyzed Through study completion, during both treatments (~4 weeks)
Primary Bench Press Power Power during bench press repetitions will be measured via a linear transducer. Through study completion, during both treatments (~4 weeks)
Primary Isometric Mid-thigh pull (IMTP) Peak Force Peak Force will be measured via dual force plates during a full-body isometric strength test. Through study completion, during both treatments (~4 weeks)
Primary Isometric Mid-thigh pull (IMTP) Rate of Force Development Rate of Force development will be measured via dual force plates during a full-body isometric strength test. Through study completion, during both treatments (~4 weeks)
Secondary Estimated Muscle Blood Flow via Near-infrared Spectroscopy (NIRS) Measures of muscle oxygenation of the anterior deltoid will be estimated using a NIRS Device. Through study completion, during both treatments (~4 weeks)
Secondary Cognitive Performance via Stroop Test The Stroop Color and Word Test (SCWT) is a neuropsychological test used to assess cognitive performance. This will be administered before and after the fatiguing bench press protocol Through study completion, during both treatments (~4 weeks)
See also
  Status Clinical Trial Phase
Completed NCT05726435 - Effects of Soluble Dietary Fiber on Sport Efficiency and Fatigue Delay in Top Basketball Players N/A
Completed NCT03822663 - The Influence of Caffeine Supplementation on Specific Performance and Training Activities Phase 3
Active, not recruiting NCT06094075 - Dynamic Strength Index-based Intervention in Basketball. N/A
Recruiting NCT05811273 - Effect of Physical Readiness Training In Badminton Players N/A
Recruiting NCT06027138 - Comparison Between Blood Flow Resistance and Slow Motion Strength Training in Wrestlers N/A
Completed NCT05576740 - Influence of Menstrual Cycle Stages on Female Athletes
Completed NCT06070064 - Effects of Trap and Reggaeton Music on Movement Velocity, Power and Muscular Endurance in the Lower Limbs of Physically Active Women N/A
Completed NCT06243341 - The Impact of MACA Supplementation on Basketball-related Performance N/A
Completed NCT04369079 - Myofascial Versus Conventional Physiotherapy N/A
Recruiting NCT05645562 - Pain Education Program in the Sport Population N/A
Completed NCT04282265 - The Effects of Red Spinach Extract on Physical Performance Following Chronic Resistance Training in Trained Males N/A
Completed NCT01727479 - Ribose and Sport Performance N/A
Completed NCT03918785 - Rice Germ Supplementation on Swimmers N/A