Sideritis Supplementation and Performance

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversity of Thessaly

About this trial

The purpose of this study is to examine the effect of sideritis consumption on physiological and performance indicators in adult subjects and compare it with the control trial.

Eligibility criteria

Qualifiers

Healthy Individuals aged 18-40 years

Disqualifiers

Musculoskeletal Injury

Dietary supplements

Medication

Trial design

Treatments tested in this trial

  • 950 mg of Sideritis Scardica (SidTea+) extract one hour pre-exercise
  • 950 mg of placebo one hour pre-exercise

Treatment groups

12 Participants
are divided into 2 treatment groups

Sponsors and collaborators