High Resistant Starch (RS) Cookies and Appetite Control

NCT ID: NCT02323828

Last Updated: 2016-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2013-06-30

Brief Summary

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Evaluation of the effect of ingestion of high RS-cookies prepared from high amylose corn starch on food intake and appetite control of a cohort of healthy students. Cookies were prepared with increasing RS content and were fed to 18 healthy students in a blind trial versus a placebo.

Parameters of interest were: short and long time intake (ad libitum test meal and 12 h diet diaries, respectively).

Detailed Description

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Conditions

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Metabolic Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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Investigational product

The investigational products are RS starch cookies (40 g resistant starch) from high amylose maize starch.

Nine young healthy volunteers (males and females) consumed RS rich cookies (40 g RS) in two separate occasions.

Group Type EXPERIMENTAL

High RS cookies

Intervention Type DIETARY_SUPPLEMENT

High RS cookies ingestion in healthy young adults

Placebo

The placebo products are common wheat-maize cookies (2 g RS). Nine young healthy volunteers (males and females) consumed placebo in two separate occasions.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

Placebo cookies ingestion in healthy young adults

Interventions

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High RS cookies

High RS cookies ingestion in healthy young adults

Intervention Type DIETARY_SUPPLEMENT

Placebo

Placebo cookies ingestion in healthy young adults

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* self-reported healthy
* not suffering disorders of lipid metabolism and eating disorders

Exclusion Criteria

* pregnant or breast-feeding
* consuming an energy-restricted diet
* vegan or vegetarians
Minimum Eligible Age

20 Years

Maximum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Catholic University of the Sacred Heart

OTHER

Sponsor Role lead

Responsible Party

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Filippo Rossi

researcher

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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24238/14

Identifier Type: -

Identifier Source: org_study_id

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