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

Phase 1
Completed
Conditions
Obesity
Interventions
Dietary Supplement: Konjac noodles
Dietary Supplement: Carbohydrate and Konjac Noodles
Dietary Supplement: Carbohydrate noodles
Registration Number
NCT01875627
Lead Sponsor
Unity Health Toronto
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Carbohydrate NoodlesKonjac noodles0g Konjac Noodles
Carbohydrate NoodlesCarbohydrate and Konjac Noodles0g Konjac Noodles
Carbohydrate NoodlesCarbohydrate noodles0g Konjac Noodles
Carbohydrate and Konjac NoodlesKonjac noodlesHalf Carbohydrate and Half Non-Caloric Konjac Noodles - 122.5g Konjac
Carbohydrate and Konjac NoodlesCarbohydrate and Konjac NoodlesHalf Carbohydrate and Half Non-Caloric Konjac Noodles - 122.5g Konjac
Carbohydrate and Konjac NoodlesCarbohydrate noodlesHalf Carbohydrate and Half Non-Caloric Konjac Noodles - 122.5g Konjac
Konjac NoodlesKonjac noodlesNon-Caloric Konjac Noodles (viscous gel meal) - 240g Konjac
Konjac NoodlesCarbohydrate and Konjac NoodlesNon-Caloric Konjac Noodles (viscous gel meal) - 240g Konjac
Konjac NoodlesCarbohydrate noodlesNon-Caloric Konjac Noodles (viscous gel meal) - 240g Konjac
Primary Outcome Measures
NameTimeMethod
Objective Satiety90 minutes

Objective 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 Outcome Measures
NameTimeMethod
Subjective Satiety90 minutes

At 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.

Trial Locations

Locations (1)

Risk Factor Modification Centre

🇨🇦

Toronto, Ontario, Canada

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