Trial · NCT02019316
BioSteel Supplementation and Performance
NCT02019316, Phase 1, Unknown, University of Western Ontario, Canada
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. BioSteel Supplementation and Performance. Trials, record NCT02019316. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02019316
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- BioSteel Supplementation and Performance
- NCT number
- NCT02019316
- Status
- Unknown
- Phases
- Phase 1
- Enrollment
- 15 participants, estimated
- Lead sponsor
- University of Western Ontario, Canada
- Conditions
- Fatigue
- Interventions
- BioSteel Sports Drink, Isoenergetic Control
- First posted
- 2013-12-24
- Last updated
- 2013-12-24
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change from baseline in Muscular Power | Baseline and following each trial (1 day). | Wingate test: Will be conducted using a cycle ergometer which electronically measures power (average, peak and decline). Resistance will be equal to 10% of subject body mass in kg. |
| Secondary | Change from baseline in Executive Function via Modified Stroop Test | Baseline and after each trial (1 day). | Modified Stroop test- a measurement of attentional fatigue and executive function, will be scored based on error rate and mean response time (Kane \& Kay, 1992). |
| Secondary | Change from baseline in anaerobic muscular power via Sitting Medicine Ball Toss | Baseline and after each trial (1 day). | Sitting medicine ball toss using a standard 4kg medicine ball. Where the ball first lands will be measured as the total distance (recorded in cm.) |
| Secondary | Change from baseline in anaerobic muscular power via Standing Long Jump | Baseline and after each trial (1 day). | Standing long jump will be conducted from a standing start with feet together. The distance from the jumping line to the individuals heels will recorded as the total distance (recorded in cm.) |
| Secondary | Change from baseline in anaerobic muscular power via Vertical Jump | Baseline and after each trial (1 day). | Vertical jump will be conducted from a standing start. Without a pre-step individual will jump as a high as possible. Measurement is to the nearest cm. |
| Secondary | Change from baseline in muscular endurance via Bench Press | Baseline and after each trial (1 day). | Bench press repetitions of 150 lbs (including the barbell) will be performed at a rate of 25 repetitions per minute. |
| Secondary | Change from baseline in speed of processing via Trail Making Test Part B | Baseline and after each trial (1 day). | Trail Making Test Part B- a measurement of visual attention and speed of processing, will be scored on total time to completion (Sanchez-Cubillo et al., 2009). |
| Secondary | Change from baseline in subjective feeling of exertion via Rating of Perceived Exertion | Baseline and after each trial (1 day) | Ratings of perceived exertion: Will be assessed after each sprint interval trial and at the conclusion of muscular endurance and power testing via a Borg Scale (Noble et al., 1983). |
Source ClinicalTrials.gov
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.
Papers8
The papers the trial lists on ClinicalTrials.gov.
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.
Tests2
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Trail Making Test B | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
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/NCT02019316
GET https://conductscience.org/api/trials/v1/NCT02019316/registered