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Satiety Response of Four Dietary Fibers

Satiety Response of Fructo-oligosaccharide (FOS), Inulin, Soluble Corn Fiber (SCF), and Resistant Starch (RS) in Overweight Woman and Relationship to Fermentation

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01233024
Enrollment
20
Registered
2010-11-02
Start date
2010-11-30
Completion date
2012-02-29
Last updated
2012-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Adult, Women, Dietary Fiber, Satiety Response, Food Intake

Brief summary

Studies have found a relationship between dietary fiber consumption and body weight regulation. This relationship may stem from enhanced satiety through fermentation of certain fibers in the large intestine. The objective of this study is to determine and compare satiety ratings, changes in food intake, and gastrointestinal effects for four fibers: fructooligosaccharide, inulin, soluble corn fiber, and resistant starch.

Interventions

DIETARY_SUPPLEMENTControl

Dinner bar fortified with 0g fiber; breakfast bar fortified with 0g dietary fiber.

DIETARY_SUPPLEMENTSoluble corn fiber

Dinner bar fortified with 12g fiber; breakfast bar fortified with 11g dietary fiber.

DIETARY_SUPPLEMENTResistant starch

Dinner bar fortified with 12g fiber; breakfast bar fortified with 11g dietary fiber.

DIETARY_SUPPLEMENTFructooligosaccharide

Dinner bar fortified with 12g fiber; breakfast bar fortified with 11g dietary fiber.

DIETARY_SUPPLEMENTInulin

Dinner bar fortified with 12g fiber; breakfast bar fortified with 11g dietary fiber.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy women * Age 18-40 years * Nonsmoking * Not taking weight loss medications * Non-dieting (weight has not changed more than 11 pounds over three months) * BMI between 18.5 and 29 * Spoken and written English literacy

Exclusion criteria

* Do not regularly consume breakfast * Food allergies to wheat, soy, peanut, or dairy * BMI less than 25 or greater than 29 upon admission to study * Cancer diagnosis in past 5 years * History of heart disease, kidney disease, diabetes, or eating disorder * History of ulcerative colitis, Crohn's disease, or any other gastrointestinal condition * History of drug or alcohol abuse in past 6 months * Use of lipid-lowering, anti-hypertensive, or anti-inflammatory steroid medication * Concurrent or recent (within 30 days) intervention study participation * Pregnant or lactating * Irregular menstrual cycle * Vegetarians * People who eat more than approximately 15 grams of fiber per day

Design outcomes

Primary

MeasureTime frameDescription
Satiety response using visual analogue scales0, 15, 30, 45, 60, 90, 120, 180 minutes postprandiallySatiety response will be measured using subjective perceptions of hunger, fullness, satisfaction, and prospective food intake evaluated by previously validated visual analogue scales (VAS).

Secondary

MeasureTime frameDescription
Food intake180 minutes postprandially and over 24 hours
Breath hydrogen response0 and 180 minutes
Gastrointestinal tolerance using visual analogue scales (VAS)24 hoursSubjective ratings of bloating, stool consistency, and flatulence will be measured using VAS. A stool count will also be recorded.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026