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Probiotic and Prebiotic Supplementation in Elite Athletes With Spinal Cord Injury

Spinal Cord Injuries Clinical Trial

Official title:
The Effect of Probiotic and Prebiotic Supplementation on Gastrointestinal Comfort in Elite Athletes With Spinal Cord Injury: A Pilot Study

Clinical Trial Summary

The main objective of this pilot study is to obtain information, which will be used for the design of a main randomized controlled trial (RCT) with a larger size based on feasibility, validity and sample size estimation as well as the potential effects of pre- and probiotic intake on intestinal microbiota. A larger trial will then be designed to test the hypothesis that adding probiotics or prebiotics may improve gut microbiome composition, gastrointestinal symptoms as well as cardiometabolic health indices in mid-term and possibly lead to improved sports performance over a longer-term period in athletes with a Spinal Cord Injury.

Clinical Trial Description

In this pilot crossover randomized controlled trial, twenty (N = 20) para-athletes will participate in an intervention consisting of a four-week intake of probiotic, using the commercially available multistrain probiotic preparation "BactoSan pro FOS" from Mepha (Basel, Switzerland), followed by a four-week wash-out period, and a four-week prebiotic intervention using "Naturaplan Bio Oat Bran" (Coop, Switzerland). Total duration of the study will be 16 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04659408
Study type Interventional
Source Swiss Paraplegic Centre Nottwil
Contact
Status Completed
Phase N/A
Start date March 1, 2021
Completion date October 29, 2021
View Details
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