Effects of Sulforaphane Supplementation on Athletic Performance
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Fatigue protocol.
- Who it may be relevant to
- Registry conditions: Nutrition, Sports. Basic parameters: 18 years — 35 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Effects of Sulforaphane Supplementation on Athletic Performance: a Double-blinded Randomized Crossover Study
Overview
Considering the promising effects observed and the scarce and incipient scientific background of SFN in sports, the present study aims to evaluate the effects of SFN supplementation on fatigue, EIMD and recovery in trained individuals. In particular, outcomes such as time to exhaustion (TTE), and perceptual questionnaires of muscle soreness, recovery, and fatigue will be assessed, aiming to explore the effectiveness of SFN.
Interventions
- Other Fatigue protocol
Fatigue protocol comprising 6 sets of 30 seconds at 120% of velocity of maximal oxygen consumption
Primary outcome measures
- time to exhaustion [Time frame: 24 hours]
Secondary outcome measures (4)
- Rating of Fatigue Scale [Time frame: Baseline, 30 minutes, 24 hours]
- Total Quality Recovery Scale [Time frame: Baseline, 30 minutes, 24 hours]
- Muscle soreness (Visual analogue scale) [Time frame: Baseline, 30 minutes, 24 hours]
- Rating of perceived exertion scale [Time frame: 30 minutes]
Eligibility criteria
Inclusion criteria
- Physically active individuals (engaging in exercise 3 or more times per week)
Exclusion criteria
- Individuals that experience musculoskeletal injuries or have experienced in the past 3 months
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Double blind
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07343518 · SFN_001