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New treatment option for Sports Nutrition
Official title Effect of a Short-term Multi-strain Probiotic Supplementation in Endurance Athletes
ClinicalTrials.gov ID: NCT07252778
What this study is testing
- What it's testing
- The aim of this project is to evaluate and identify the effect of a short-term 2-week multi-strain probiotic (MPRO) supplementation on the exercise-associated gastrointestinal (GI) symptoms and perturbations in high level female athletes of the Polish national team during strictly controlled conditions of a training camp, based on recommendations for best practices for probiotic (PRO) research in athletes and assessment of EX-associated GI perturbations.
- Phase 3: a large, late-stage study
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 16 to 50, women only. Healthy volunteers may be eligible.
You may be able to join if
- belonging to the national rowing team;
- training experience ≥5 years;
- a currently issued medical certificate confirming
- good health and capacity to practice sports;
- good health without chronic health disorders;
You likely can't join if
- injury, any health contraindication or failure to perform exercise procedures;
- gastrointestinal infections, diseases, disorders;
- past history of gastrointestinal surgery, and
- other self-reported gastrointestinal issues;
- reporting symptoms of infection or taking any medication (e.g. antibiotics) for 4 weeks before the study protocol;
- current supplementation of prebiotics,
See the full eligibility criteria
- belonging to the national rowing team;
- training experience ≥5 years;
- a currently issued medical certificate confirming
- good health and capacity to practice sports;
- good health without chronic health disorders;
- written informed consent to participate.
- injury, any health contraindication or failure to perform exercise procedures;
- gastrointestinal infections, diseases, disorders;
- past history of gastrointestinal surgery, and
- other self-reported gastrointestinal issues;
- reporting symptoms of infection or taking any medication (e.g. antibiotics) for 4 weeks before the study protocol;
- current supplementation of prebiotics,
- probiotics, synbiotics (last 4 weeks);
- current intake of pharmaceutical agents (e.g., nonsteroidal anti-inflammatory drugs, laxatives, antidiarrhea agents, antacids, and/or antiemetics) (last 4 weeks);
- failure to follow the study protocol;
- declared general feeling of being unwell;
- pregnancy or current pregnancy planning.
The study team makes the final eligibility decision.
Where it's taking place
- Poznan, Wielkopolska, Poland
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 16 years to 50 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Poznan, Wielkopolska, Poland. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.