Soccer

2

Review clinical trials related to Soccer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The Effect of Individual Sodium Citrate Consumption on Repeated Sprint Performance in Female Soccer Players

The aim of this research is to determine whether sodium citrate supplementation, taken at the best individual time, would improve repeated sprint performance in professional female soccer players. The main questions it aims to answer are: 1. Does sodium citrate improve sprint times, peak power, minimum power, and mean power during repeated sprints? 2. Does sodium citrate lower fatigue index (the drop in power across sprints) during repeated sprint exercise? 3. Does sodium citrate change blood bicarbonate, pH, and lactate levels before and after exercise? 4. Does sodium citrate affect how hard exercise feels (perceived exertion)?

Participants needed: 20
Trial details
Age: 18-25Biological sex: FemaleType: InterventionalSponsor: Hacettepe UniversityUpdated: Jul 30, 2026
Eligibility criteria

Female professional soccer players competing in the Turkish Women's Third League [+6]

Use of oral contraceptives [+6]

Status: Not yet recruiting

Isometric vs. Dynamic Squat Pre-Loading: Acute PAPE Responses

This randomized crossover study compared the acute post-activation performance responses to isometric and dynamic squat-based preconditioning protocols performed with and without electromyostimulation (EMS). Participants completed five randomized experimental conditions: maximal voluntary isometric contraction (MVIC), dynamic contraction (DC), MVIC+EMS, DC+EMS, and EMS only (O-EMS). Baseline and post-intervention assessments included countermovement jump (CMJ), countermovement jump with arm swing (CMJWH), zig-zag agility, and shooting speed, with post-tests conducted after a 4-minute recovery period. Perceptual responses, including ratings of perceived exertion (RPE), perceived discomfort (RPD), and fatigue (VAS), were recorded immediately after each protocol. All sessions were conducted between 14:00 and 16:00 under standardized conditions, with protocol order randomized and participants instructed to avoid strenuous exercise and food intake before testing.

Participants needed: 22
Trial details
Age: 18-25Biological sex: MaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jul 10, 2026Locations: 1
Eligibility criteria

Being healthy [+2]

Being under 18 years old [+2]