Hypertension
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants aged 18 to 35 years; both sexes; absence of clinical conditions; no continuous use of medications such as diuretics, corticosteroids, or beta-blockers; no dietary restrictions (lactose intolerance, gluten allergy, cow's milk protein allergy); non-smokers; physically active
Exclusion criteria
Exclusion criteria: Functional limitation, family history of cardiovascular diseases, use of food supplements (especially thermogenic/slimming supplements), being a regular consumer of coffee (usual intake estimated at up to 100 mg/day), teas and/or soft drinks that contain caffeine in their formulation and consume other stimulant drinks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome found 1: Only the 500 mg caffeine dose elicited an increase in the fat oxidation rate—which began 60 minutes after ingestion and remained elevated until the end of the experiment—compared to the other experimental conditions (p-value = 0.00187). Caffeine supplementation at various doses did not affect hemodynamic variables during the 120-minute period compared to the placebo (p-value > 0.05);Expected outcome 1:Changes in fat oxidation rate (mg/min), blood pressure (mmHg), and serum triglyceride levels (mg/dL) are expected to be identified after the ingestion of different doses of caffeine by comparing the values obtained before and after each intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: Changes in the carbohydrate oxidation rate (mg/min) are expected to be identified following the ingestion of different doses of caffeine, comparing values ??obtained before and after each intervention;Outcome found 2: Resting energy expenditure and the carbohydrate oxidation rate were not altered by caffeine supplementation under any of the experimental conditions (P-value > 0.05) | — |
Countries
BR
Contacts
Universidade Federal de Ciências da Saúde de Porto Alegre