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Satiety Study of a Carbohydrate Meal to a Highly Viscous Gel Meal

Comparing the Satiety Scores of a Carbohydrate Meal to a Meal of Equal Volume in Which Half of the Volume is Replaced With a Highly Viscous Gel.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01875627
Acronym
InGel
Enrollment
15
Registered
2013-06-12
Start date
2010-11-30
Completion date
2012-01-31
Last updated
2013-06-12

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

Conditions

Obesity

Brief summary

To evaluate the effects of Konjac on satiety and subsequent food intake in healthy individuals.

Interventions

DIETARY_SUPPLEMENTKonjac noodles

Replacement of carbohydrate noodles with non-caloric Konjac noodles (viscous gel meal)

DIETARY_SUPPLEMENTCarbohydrate and Konjac Noodles
DIETARY_SUPPLEMENTCarbohydrate noodles

Sponsors

Unity Health Toronto
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Men and women * Age 18-65 years * Having a BMI of 18.5 - 25 kg/m2 * No presence of major disease

Exclusion criteria

* Known history of liver or kidney disease, diabetes, hypertension, stroke or myocardial infarctions, thyroid disease, gastrointestinal disease, AIDS or AIDS-related complications; subjects using prescription medications or Natural Health Products; Subjects will be excluded if they have any condition which, in the opinion of the investigator, might jeopardize the health and safety of the subject or study personnel, or adversely affect the study results

Design outcomes

Primary

MeasureTime frameDescription
Objective Satiety90 minutesObjective satiety will be measured through subsequent food intake. At each visit, participants will consume a pre-weighed snack (wafer cookies) that will be administered ad libitum at 90mins after consumption of the test meal. Subsequent food intake will be calculated by weighing the amount of the snack food left after consumption.

Secondary

MeasureTime frameDescription
Subjective Satiety90 minutesAt each visit, participants will record their subjective satiety ratings using a 100 mm visual analogue scale and these rating will be combined into a total subjective appetite score using the formula (Q1+Q2+(100-Q3)+Q4)/4.

Countries

Canada

Outcome results

None listed

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