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Effect of Different Fiber Breakfasts on Appetite and Weight Change in Overweight Subjects

The Effect of Ingesting Breakfasts Varying in Fiber on Appetite and Weight Change in Overweight Subjects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02035150
Enrollment
36
Registered
2014-01-14
Start date
1998-03-31
Completion date
2002-12-31
Last updated
2014-01-14

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

Conditions

Obesity

Keywords

breakfast, oatmeal, appetite, cholesterol

Brief summary

Regular breakfast consumption may help lower body weight reduce body fatness and improve cardiovascular disease risk factors. However, the best kind of breakfast to consume to achieve these effects is unclear. We hypothesized that a high fiber breakfast would suppress appetite, lower body weight and improve cardiovascular disease risk factors compared with a no-fiber breakfast.

Detailed description

Participants will report to the hospital cafeteria between 0800 and 0900h following an overnight fast every weekday for 4 consecutive weeks. On arrival, participants will be provided will the allocated breakfast and will be given 15 min to consume all the foods provided. The oatmeal breakfast will consist of 80g dry oatmeal (Quaker Quick Oats) prepared with 120mL fat-free milk and 230mL water. The frosted flakes breakfast will consist of 62g frosted flakes and 160mL whole milk and 190mL water served on the side. The No-breakfast (control) will consist of only 350mL plain water. All participants will also receive 200mL decaffeinated coffee with 12mL non-dairy creamer and 1g packet of non-caloric sweetener. On Friday of each week participants will be provided with two portions of the breakfasts to take home at consume on the weekend days. On the first day of the intervention and weekly thereafter participants will complete 3hr subjective appetite ratings responses to the breakfast. Laboratory assessments including body weight, composition, blood pressure and a fasting blood sample will be collected before the start of the intervention and at the end of the intervention.

Interventions

DIETARY_SUPPLEMENTNo Breakfast

A breakfast consisting of plain water

DIETARY_SUPPLEMENTOatmeal

A breakfast consisting of oatmeal

DIETARY_SUPPLEMENTFrosted Flakes

A breakfast consisting of Frosted Flakes and milk

Sponsors

PepsiCo Global R&D
CollaboratorINDUSTRY
New York Obesity and Nutrition Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI \>27kg/m2 * Weight stable (\<5% weight change in past 3 months)

Exclusion criteria

* Smokers * Regular use of medications * Currently undertaking a weight-loss or exercise program * Females who are pregnant or lactating

Design outcomes

Primary

MeasureTime frameDescription
Change in body weightChange in body weight over 4 week interventionBody weight will be measured at baseline and following 4-week breakfast intervention

Secondary

MeasureTime frameDescription
Subjective appetiteAppetite ratings in response to breakfast will be collected for 3hs on the first day of the study and after 1, 2, 3 and 4 weeks of the interventionRatings of hunger and Fullness will be collected on a 6 point rating scale with 0 labelled not at all, 40 moderately, 60 quite, 80 very and 100 extremely.
Change in plasma metabolic risk factorsAt baseline and following 4-week interventionA fasting blood sample will be collected and analyzed for glucose, insulin, triacylglycerol, leptin and cholesterol
Resting Energy ExpenditureResting energy expenditure will be measured at baseline and following the 4 week interventionResting energy expenditure measurements will be collected whilst subjects are fasting, resting in a semi-supine position under thermoneutral conditions with a ventilated hood and metabolic cart.

Other

MeasureTime frameDescription
Blood pressureAt baseline and following 4-week interventionSystolic and diastolic blood pressure will be measured at baseline and following 4-week intervention

Outcome results

None listed

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