Study Results
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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UNKNOWN
NA
32 participants
INTERVENTIONAL
2014-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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Cherry flavoured beverage 1
10floz cherry flavoured test article
No interventions assigned to this group
Cherry flavoured beverage 2
10floz of cherry flavoured test article with fruit, vegetable and herbal extracts
Beverage containing plant based extracts
Intervention involves single exposure, oral consumption of test article following baseline measurements
Cherry flavoured beverage 3
10floz of cherry flavoured test article with fruit, vegetable and herbal extracts
Beverage containing plant based extracts
Intervention involves single exposure, oral consumption of test article following baseline measurements
Cherry flavoured beverage 4
10floz of cherry flavoured test article with fruit, vegetable and herbal extracts
Beverage containing plant based extracts
Intervention involves single exposure, oral consumption of test article following baseline measurements
Interventions
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Beverage containing plant based extracts
Intervention involves single exposure, oral consumption of test article following baseline measurements
Eligibility Criteria
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Inclusion Criteria
* Self-report of good health
Exclusion Criteria
* Are below 18 or above 49 years of age
* Are a smoker
* Have food allergies or sensitivities to any of the ingredients contained in the investigational product or any other foodstuff
* Currently take medication except the contraceptive pill
* Have habitually used dietary supplements within the last month (defined as more than 3 consecutive days or 4 days in total)
* Have sleep disturbances and/or are taking sleep aid medication
* Have a Body Mass Index (BMI) outside of the range 18-35 kg/m2
* Have high blood pressure (systolic over 139 mm Hg or diastolic over 89 mm Hg)
* Have a history of neurological, vascular or psychiatric illness including epilepsy or seizures (excluding depressive illness and anxiety)
* Have a current diagnosis of anxiety or depression
* Are pregnant, trying to get pregnant or breast feeding
* Have a recent history of (within 12 months of screening visit) or strong potential for alcohol or substance abuse. Alcohol abuse is defined as more than 60g (men) / 40g (women) pure alcohol per day (7 / 5.5 units)
* Are (or are seeking to become) pregnant or are lactating
* Have learning difficulties, dyslexia or colour blindness
* Have visual impairment that cannot be corrected with glasses or contact lenses
* Have frequent migraines that require medication (more than or equal to 1 per month)
* Have disorders of the blood
* Have a heart disorder or a history of vascular illness
* Have a respiratory disorder that requires regular medication (Note: participants with asthma who only take their medication occasionally/as required are eligible for this study)
* Have type I or type II diabetes
* Have a history of renal or hepatic disease, or other severe diseases of the gastrointestinal tract (e.g. iron accumulation, iron utilization disorders, hypercalcaemia, hypercalciuria), that are likely to interfere with metabolism/absorption/secretion of the product under investigation
* Have any health condition that would prevent fulfillment of the study requirements
* Are currently or have in the past 4 weeks participated in other clinical or nutrition intervention studies
* Do not have a bank account (required for payment)
18 Years
49 Years
ALL
Yes
Sponsors
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PepsiCo Global R&D
INDUSTRY
Responsible Party
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Locations
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Northumbria University
Newcastle upon Tyne, , United Kingdom
Countries
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Central Contacts
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Other Identifiers
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PEP-1406
Identifier Type: -
Identifier Source: org_study_id
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