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Trial · NCT04292106

The Effects of Red Spinach Extract Supplementation on Isometric Strength, Resistance Exercise and Cognitive Performance

NCT04292106, Not applicable, Completed, Lipscomb University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Effects of Red Spinach Extract Supplementation on Isometric Strength, Resistance Exercise and Cognitive Performance. Trials, record NCT04292106. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04292106

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Effects of Red Spinach Extract Supplementation on Isometric Strength, Resistance Exercise and Cognitive Performance
NCT number
NCT04292106
Status
Completed
Phases
Not applicable
Enrollment
11 participants, actual
Lead sponsor
Lipscomb University
Conditions
Sports
Interventions
Red Spinach Extract (RSE), Placebo
First posted
2020-03-02
Last updated
2022-01-14

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBench Press Repetitions to FatiugeThrough study completion, during both treatments (~4 weeks)Number of repetitions completed in each set during the acute exercise bout will be recorded and analyzed
PrimaryBench Press PowerThrough study completion, during both treatments (~4 weeks)Power during bench press repetitions will be measured via a linear transducer.
PrimaryIsometric Mid-thigh pull (IMTP) Peak ForceThrough study completion, during both treatments (~4 weeks)Peak Force will be measured via dual force plates during a full-body isometric strength test.
PrimaryIsometric Mid-thigh pull (IMTP) Rate of Force DevelopmentThrough study completion, during both treatments (~4 weeks)Rate of Force development will be measured via dual force plates during a full-body isometric strength test.
SecondaryEstimated Muscle Blood Flow via Near-infrared Spectroscopy (NIRS)Through study completion, during both treatments (~4 weeks)Measures of muscle oxygenation of the anterior deltoid will be estimated using a NIRS Device.
SecondaryCognitive Performance via Stroop TestThrough study completion, during both treatments (~4 weeks)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

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests1

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed as
Stroop Color-Word TestSecondary outcome

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04292106

GET https://conductscience.org/api/trials/v1/NCT04292106/registered