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Fiber Supplement

Dietary Fibers for Aerobic Endurance

N/A
Recruiting
Led By J. Philip Karl, PhD
Research Sponsored by United States Army Research Institute of Environmental Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Females must have normal menstrual cycles between 26-32 days in duration; 5 menstrual cycles within the past 6 months; or be using an oral/hormonal contraceptive which contains low-dose estrogen/progesterone to maintain continuous levels throughout the 28-day cycle (i.e., no placebos)
Self-reports a usual bowel movement frequency of every other day or more often
Timeline
Screening 3 weeks
Treatment Varies
Follow Up phases 1 and 2, day 8. measured fasted (-300minutes) and before (0minutes), during (40minutes) and at the end (80minutes) of steady state endurance exercise.
Awards & highlights

Study Summary

This trial will study how adding certain fibers to diets affects exercise performance & how biological changes may explain results.

Who is the study for?
This trial is for healthy, active-duty adults aged 18-39 who exercise regularly and meet Army body composition standards. Women must have normal menstrual cycles or be on low-dose hormonal contraceptives. Participants must avoid caffeine, alcohol, nicotine, dietary supplements, and certain foods before and during the study. Exclusions include GI issues, recent colonoscopy, pregnancy/breastfeeding, metabolic/cardiovascular abnormalities, anemia/sickle cell trait/disease.Check my eligibility
What is being tested?
The study tests how short-chain fatty acids (SCFAs) from high amylose maize starch affect aerobic endurance compared to a placebo of low amylose maize starch in physically active adults. It's a randomized double-blind crossover trial with two one-week diet periods separated by at least two weeks. Endurance exercises are performed post-diet; biological samples are collected to analyze metabolism and gut health.See study design
What are the potential side effects?
Potential side effects may include gastrointestinal discomfort due to changes in fiber intake from the SCFA-enriched diets or allergic reactions to ingredients in the provided foods. However, as this is a nutrition-based intervention involving commonly consumed substances rather than novel drugs or treatments, significant side effects are not typically expected.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My menstrual cycles are regular, between 26-32 days, or I am on a specific birth control.
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I usually have bowel movements every other day or more frequently.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~phases 1 and 2, day 8. measured fasting (-300minutes) and before (0minutes) and at the end (80minutes) of steady state endurance exercise
This trial's timeline: 3 weeks for screening, Varies for treatment, and phases 1 and 2, day 8. measured fasting (-300minutes) and before (0minutes) and at the end (80minutes) of steady state endurance exercise for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Run time
Secondary outcome measures
Fecal short-chain fatty acid concentrations
Intestinal pH
Intestinal permeability
+4 more
Other outcome measures
Appetite
Breath hydrogen and methane
Circulating biomarkers of gut barrier function
+13 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: High-amylose maize starch+acetate/butyrateActive Control1 Intervention
High-amylose maize starch, (Hylon VII; Ingredion, Inc.) to which the SCFA acetate or butyrate has been chemically added.
Group II: Low-amylose maize starchPlacebo Group1 Intervention
Low-amylose maize starch (AMIOCA; Ingredion, Inc).

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
SCFA-enriched high amylose maize starch increases colonic SCFA content through the fermentation of resistant starch by gut microbiota. SCFAs, such as acetate, propionate, and butyrate, regulate energy homeostasis, improve gut health, and modulate inflammation. They enhance insulin sensitivity, reduce fat accumulation, and provide energy for colonocytes. This is crucial for metabolism patients as it helps manage metabolic disorders like obesity, type 2 diabetes, and metabolic syndrome by improving metabolic health and reducing associated risks.

Find a Location

Who is running the clinical trial?

United States Army Research Institute of Environmental MedicineLead Sponsor
61 Previous Clinical Trials
3,438 Total Patients Enrolled
J. Philip Karl, PhDPrincipal InvestigatorUnited States Army Research Institute of Environmental Medicine
1 Previous Clinical Trials
33 Total Patients Enrolled
~7 spots leftby Jun 2025