Evaluation of Metabolism-Boosting Beverages

NCT ID: NCT01029236

Last Updated: 2009-12-09

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

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2007-12-31

Brief Summary

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The purpose of this study is to assess the effect of Metabolism-boosting Beverages (MBB) containing green tea extract with a standardized amount of epigallocatechin gallate (EGCG) and caffeine.

Detailed Description

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The study will assess the effect of MBB's on 24 hour energy expenditure by performing indirect calorimetry, and on appetite using visual analogue scales (VAS). The planned sample size is 54 healthy male and female adults, both lean and overweight. We plan to test 6 metabolism-boosting beverages in the following order: 1) Raspberry Tea 2) Banana Shake 3) Chai Latte 4) Strawberry Shake 5) Cappuccino 6) Hot Cocoa. In the order that they are screened, each subject will be assigned to receive 1 of 6 Metabolism-boosting beverages. Each MBB will contain 90 mg EGCG and 100 mg caffeine.

Conditions

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Energy Expenditure Appetite

Keywords

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obesity metabolism weight loss energy expenditure thermogenesis Metabolism-Boosting Beverages effect on REE Metabolism-Boosting Beverages effect on appetite

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Interventions

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Medifast Metabolism-boosting Beverages

Medifast metabolism-boosting beverages containing 90 mg EGCG and 100 mg caffeine.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult males and females (age between 18 and 65)
* BMI ≥18.5 - ≤ 40.0 kg/m2
* Non-smokers
* No known food allergies to wheat, gluten, soy or nuts
* ≤ 14 alcoholic beverages per week
* No sensitivity to caffeine or green tea
* No alcohol or caffeine on days when metabolism is tested
* Willing and able to give informed consent
* Not currently using appetite-affecting medications (e.g SSRIs, steroids, Ritalin)
* Not pregnant or lactating

Exclusion Criteria

* Actively dieting
* Chronic uncontrolled health problems (not including obesity or controlled: type-2 diabetes, hyperlipidemia, hypertension)
* History of arrhythmia, or taking anti-arrhythmic medications (e.g. propafenone)
* Schizophrenia, history of bipolar disorder, current Major Depressive Disorder
* Dependence on alcohol or sedative-hypnotic drugs (e.g. benzodiazepines)
* Cognitive impairment severe enough to preclude informed consent
* Taking weight loss or appetite-suppressant medications
* Taking appetite affecting medications (e.g. SSRIs, steroids, Ritalin)
* Food allergies to wheat, gluten, soy, or nuts
* Sensitivity to caffeine or green tea
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medifast, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Medifast Inc.

Principal Investigators

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Lisa M Davis, PhD, PA-C

Role: PRINCIPAL_INVESTIGATOR

Medifast, Inc.

Christopher D Coleman, MS,RD,LDN

Role: STUDY_DIRECTOR

Medifast, Inc.

Locations

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Medifast Inc.

Owings Mills, Maryland, United States

Site Status

Countries

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United States

References

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Other Identifiers

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20070530

Identifier Type: OTHER

Identifier Source: secondary_id

MED010

Identifier Type: -

Identifier Source: org_study_id