← Back to all trials
Completed
NCT06648967
Impact of Different Carbohydrate Feedings on a Hydrogen Breath Curve and Self-reported Gastrointestinal Complaints
Conditions: Quality of Life
Sex: All
Ages: 18 Years – 60 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 8
Sponsor: Arizona State University
Location: Health Futures Center Phoenix Arizona
Summary
GI distress is widely prevalent among athletes, ranging from 30 to 90% in recreationally and professionally active athletes. As the recipient of nutrients, the gastrointestinal (GI) tract plays an important role in athleticism. The following pilot project aims to better understand if a fructose load after hiking under heat stress will result in a meaningful hydrogen breath elevation as a marker for malabsorption in healthy participants, and if supplementation of a multi-ingredient fermented whey supplement will result in a different hydrogen breath response rate after a heat stress hiking test.
Eligibility Criteria
Inclusion Criteria:
* Healthy subjects living in the United States.
* Women/Men aged between 18-60 years (50-50%).
* BMI value between ≥18.5 and ≤ 30 kg/m2.
* No physical limitations (i.e., able to perform all activities associated with daily living in an independent manner).
* Written informed consent.
* Completed PAR-Q+ without any "yes" responses.
* If currently using chronically or intermittently, willing to stop taking pre- and probiotics beginning 1 month prior to and throughout data collection.
* If currently using chronically or intermittently, willing to stop using laxatives or fiber supplements, antacids and prokinetics beginning 1 month prior to and throughout data collection.
Exclusion Criteria:
* Smoking.
* Clinical or self-perceived lactose intolerance.
* Clinical or self-perceived milk protein allergy.
* Diagnosed GI tract disorders or diseases.
* Musculoskeletal disorders.
* Diagnosed metabolic disorders (such as diabetes).
* Use of any medications known to affect protein metabolism (i.e., corticosteroids, non-steroidal anti-inflammatories, or prescribed acne medications).
* Chronic use of gastric acid suppressing medication or anti-coagulants.
* Chronic use of anti-inflammatory medication.
* Unwilling to stop taking pre- and probiotics beginning 1 month prior to and throughout data collection.
* Unwilling to stop using laxatives or fiber supplements, antacids and prokinetics beginning 1 month prior to and throughout data collection.
Source: ClinicalTrials.gov (NCT06648967). StuddyBuddy aggregates publicly available trial information.