Clinical TrialID 8024
Beta-alanine Supplementation and CrossFit Performance
NCT05772988
Exercise-Induced Lactic Acidemia
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 8024
- Evidence Id
- 8024
- Core Evidence Id
- 8024
- Source Clinical Trial Id
- 8018
- Herb2 Clinical Trial Id
- HBCT008018
- Nct Id
- NCT05772988
- Title
- Beta-alanine Supplementation and CrossFit Performance
- Status
- Completed
- Phase
- Study Result
- No
- Study Condition
- Exercise-Induced Lactic Acidemia
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
- Intervention
- DIETARY_SUPPLEMENT: Beta-alanine|DIETARY_SUPPLEMENT: Maltodextrin
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Triple
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 12
- Outcome Measure
- Change from baseline in time to perform a "Fran" CrossFit workout, This involves alternating sets of dumbbell thrusters and pull-uips, Baseline, 3 weeks
- Sponsor Collaborator
- University of Saskatchewan
- Funded By
- OTHER
- Location
- University of Saskatchewan, Saskatoon, Saskatchewan, S7N5B2, Canada
- Other Id
- 2022_23_02
- Start Date
- 2023-03-15
- Primary Completion Date
- 2023-08-31
- Completion Date
- 2023-08-31
- First Posted
- 2023-03-17
- Results First Posted
- Last Update Posted
- 2024-05-29
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05772988
- Title Cn
- Title En
- Beta-alanine Supplementation and CrossFit Performance
- Bilingual Status
- semi_complete