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Satiety, Glycemic, and Gastrointestinal Effects of Novel Fibers

Satiety, Glycemic, and Gastrointestinal Effects of Novel Fibers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00958399
Enrollment
20
Registered
2009-08-13
Start date
2008-07-31
Completion date
2010-04-30
Last updated
2012-02-06

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

Conditions

Healthy

Keywords

satiety, fiber, food intake, gut hormones, visual analog scales, microflora

Brief summary

Research suggests dietary fiber may play a role in weight management, and fiber consumption is inversely associated with body weight, body fat, and BMI in cross-sectional studies. These effects may be mediated by increased satiety, reduced food intake, or changes in blood levels of glucose, insulin, and gut hormones. The purpose of this study is to determine the satiety, glycemic, hormonal, and gastrointestinal responses of novel fiber supplements.

Interventions

DIETARY_SUPPLEMENTPlacebo

Low fiber muffin, hot cereal and beverage (acute phase) or fiber bars and beverage (chronic phase)

DIETARY_SUPPLEMENTResistant Starch

25 g resistant starch, administered in a muffin, hot cereal and beverage (acute phase) or fiber bars and beverage (chronic phase)

DIETARY_SUPPLEMENTResistant starch + soluble fiber

25 g fiber as resistant starch and a soluble fiber, administered in a muffin, hot cereal and beverage (acute phase) or fiber bars and beverage (chronic phase)

DIETARY_SUPPLEMENTFiber made from corn starch

25 g fiber made from corn starch, administered in a muffin, hot cereal and beverage (acute phase) or fiber bars and beverage (chronic phase)

DIETARY_SUPPLEMENTFiber made from corn starch + soluble fiber

25 g fiber as a fiber made from corn starch and a soluble fiber, administered in a muffin, hot cereal and beverage (acute phase) or fiber bars and beverage (chronic phase)

Sponsors

Tate and Lyle Ingredients France
CollaboratorINDUSTRY
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy men and women * age 18-60 years * non-smoking * not taking medication * non-dieting (weight stable in prior 3 months) * BMI 18-27 * English literacy * ability to give blood

Exclusion criteria

* do not regularly consume breakfast * food allergies to ingredients found in study products * dislike for muffins, fiber bars, or hot cereal * BMI \<18 or \>27 * diagnosed cardiovascular, renal, or hepatic disease * diabetes mellitus (fasting blood sugar \>126 mg/dl) * cancer in previous 5 years (except basal cell carcinoma of the skin) * any gastrointestinal disease or condition * recent bacterial infection (\< 3 months) * recent or concurrent participation in an intervention research study * history of drug or alcohol abuse in prior 6 months * use of lipid-lowering, anti-hypertensive, or anti-inflammatory steroid medication * restrained eaters * vegetarians * people who eat more than approximately 15 grams of fiber per day * women who are pregnant or lactating * women with irregular menstrual cycles

Design outcomes

Primary

MeasureTime frame
Satiety0, 15, 30, 45, 60, 90, 120, 180, 215 minutes postprandially

Secondary

MeasureTime frame
ad libitum food intake180 minutes postprandially and over 24 hours
Ghrelin, polypeptide YY (PYY), and glucagon-like peptide-1 (GLP-1) response0, 30, 60 minutes postprandially
Gastrointestinal tolerance and fecal chemistryfollowing 7 days of treatment
Glucose/Insulin Response0, 15, 30, 45, 60, 90, 120, 180 minutes postprandially

Countries

United States

Outcome results

None listed

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