The Effects of Processed Whole Orange on Subjective Ratings of Satiety

NCT ID: NCT02116023

Last Updated: 2014-10-28

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

2014-03-31

Brief Summary

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The study is a human dietary test meal study that is a randomized, controlled, double blind, cross over design with 3 intervention arms that will investigate the subjective ratings of satiety in response to different levels of processed whole orange compared with a sugar-matched isocaloric control

Detailed Description

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Conditions

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Self Reported Ratings of Hunger

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Orange flavored beverage - Test1

240ml processed whole orange low dose

Group Type EXPERIMENTAL

Orange flavored beverage

Intervention Type OTHER

Orange flavored beverage - Test2

240ml processed whole orange high dose

Group Type EXPERIMENTAL

Orange flavored beverage

Intervention Type OTHER

Orange flavored beverage - Placebo

240ml orange beverage

Group Type PLACEBO_COMPARATOR

Orange flavored beverage

Intervention Type OTHER

Interventions

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Orange flavored beverage

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Gender: male or female
* Age at start of the study: males and females ≥ 21and ≤ 65 years
* Females taking contraceptive pill or post menopausal
* Body Mass Index (BMI) ≥ 18.5 and ≤ 27 kg/m2
* Apparently healthy: measured by questionnaire, no reported current or previous -metabolic diseases or chronic gastrointestinal disorders
* Reported dietary habits: no medically prescribed diet, no slimming diet within the past 3 months, used to eating 3 meals a day
* Reported intense sporting activities ≤ 10h/w
* Reported alcohol consumption ≤21 units/w Informed consent signed
* Recruitment form filled out

Exclusion Criteria

* Smoking
* Premenopausal females not taking the contraceptive pill
* Dislike, allergy or intolerance to test products
* Possible eating disorder (measured by SCOFF questionnaire score \>1)
* Eating habits questionnaire score \>14
* Reported medical treatment that may affect eating habits/satiety
* Food allergies or intolerance
Minimum Eligible Age

21 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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PepsiCo Global R&D

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of Reading

Reading, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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PEP-1402

Identifier Type: -

Identifier Source: org_study_id

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