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GLOSSARY

Key Terms & Definitions for Health Sciences

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Evidence-Based Ergogenic Aids Table

Nutrition & Sports Nutrition Reference Tables

Evidence-Based Ergogenic Aids Table

Evidence categories describe efficacy in specific contexts and do not replace safety, legality or product-quality assessment.

Category or example Evidence context Decision point
Creatine monohydrate Repeated high-intensity effort and training adaptation Useful for selected goals
Caffeine Selected endurance and high-intensity tasks Dose, sleep and individual response matter
Nitrate, beta-alanine, bicarbonate Specific exercise contexts Protocol and tolerance are important
Limited or inconsistent evidence Many marketed ingredients and combinations Do not infer benefit from a biochemical mechanism
Prohibited or high-risk substances Separate anti-doping and safety assessment Do not use an efficacy score as permission

Supplement Evidence is the body of scientific information supporting a particular claim. Quality, consistency, relevance and uncertainty matter alongside the number of studies.

A credible supplement claim needs relevant controlled evidence, an appropriate comparison and a meaningful outcome. Randomization, placebo control and blinding reduce different sources of bias but do not guarantee a useful result. Sample size, uncertainty, training status, sex, diet and protocol affect interpretation. A pooled estimate is not a promise to every individual. Mechanistic plausibility, a changed biomarker, exercise capacity and actual competition performance are distinct levels of information that should not be treated as interchangeable.

Apparent individual responses combine biological variation, measurement error, expectations and changes in training or diet. A person classified as a nonresponder after one noisy test may not have a stable absence of benefit. Use repeated, relevant observations under comparable conditions and consider starting nutrient status or habitual intake. Genetic mechanisms can be informative without making a commercial genetic test a validated prescription. Individualization should improve a practical decision, not turn uncertain differences into permanent athlete labels.

A nutritional strategy should be evaluated by the quality and relevance of evidence, the athlete's response and the feasibility of implementation. Molecular signaling, a substrate-oxidation change, a laboratory capacity test and race performance are different outcomes. Association does not establish cause, and a response in one small study need not generalize to all athletes. Define the intended benefit before changing the plan, then evaluate training quality, recovery and performance under comparable circumstances rather than judging success by novelty.

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