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Trial registered on ANZCTR
Registration number
ACTRN12610001048077
Ethics application status
Approved
Date submitted
24/11/2010
Date registered
30/11/2010
Date last updated
31/01/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Cognitive and heart health benefits of chewing after eating green leafy vegetables
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Scientific title
Cognitive and heart health benefits of chewing after eating green leafy vegetables in healthy men and women
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Secondary ID [1]
253160
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cardiovascular disease
258708
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Cognitive function
258709
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Condition category
Condition code
Cardiovascular
258863
258863
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0
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Coronary heart disease
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Diet and Nutrition
258864
258864
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0
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Other diet and nutrition disorders
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Cardiovascular
258865
258865
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0
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Hypertension
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A randomized controlled crossover-design trial will be conducted to investigate the acute effects of chewing gum on metabolism of nitrogen oxides, as well as neurocognitive performance outcome measures and endothelial function.
Each participant will complete 2 visits in random order with a minimum of one week washout between each visit. Prior to each visit participants will be asked to consume a standard meal for dinner. For each visit participants will attend the School of Medicine and Pharmacology Research Unit at Royal Perth Hospital in the morning after standard low nitrate breakfast. They will be randomly allocated to:
1. No chewing
2. Chewing
Participants will consume a standardized lunch containing a fixed level of nitrate derived from spinach. They will begin chewing gum 30 minutes after lunch and continue chewing for 2 hours. A fruit-flavoured, sugar-free chewing gum will be used.
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Intervention code [1]
257664
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Treatment: Other
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Comparator / control treatment
No chewing after a standardised lunch containing a fixed level of nitrate derived from spinach.
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Control group
Active
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Outcomes
Primary outcome [1]
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Plasma nitrite concentration measured using gas chromatography-mass spectrometry
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Assessment method [1]
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Timepoint [1]
259718
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Baseline and 2 hours after lunch
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Primary outcome [2]
259719
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Nitric oxide status assessed by measuring plasma S-nitrosothiols
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Assessment method [2]
259719
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Timepoint [2]
259719
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Baseline and 2 hours after lunch
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Secondary outcome [1]
266448
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Salivary nitrate and nitrite concentrations measured using gas chromatography-mass spectrometry
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Assessment method [1]
266448
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Timepoint [1]
266448
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Baseline and 45 minutes after lunch
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Secondary outcome [2]
266449
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Blood pressure measured using an automated blood pressure monitor
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Assessment method [2]
266449
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Timepoint [2]
266449
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Baseline and 60, 90 and 120 minutes after lunch
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Secondary outcome [3]
266450
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Neurocognitive performance assessed using the COMPASS neuropsychological test battery.
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Assessment method [3]
266450
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Timepoint [3]
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Baseline and 1 hour after lunch
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Secondary outcome [4]
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Endothelial function assessed by measuring flow-mediated dilatation of the brachial artery using ultrasound.
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Assessment method [4]
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Timepoint [4]
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Baseline and 90 minutes after lunch
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Eligibility
Key inclusion criteria
Healthy men and women aged 20 to 70 years
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Minimum age
20
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
1.Current or recent (<12 months) smoking
2.Body mass index < 18 or > 35 kg/m2,
3.History of cardiovascular or peripheral vascular disease,
4.A systolic blood pressure below 100 or above 160 mmHg
5.A diastolic blood pressure below 50 or above 100 mmHg
6.Diagnosed diabetes, and non-diabetic individuals with fasting plasma glucose concentrations greater than or equal to 5.5 mmol/L,
7.A psychiatric illness,
8.Other major illnesses such as cancer,
9.Current or recent (within previous 6 months) significant weight loss or gain (> 6% of body weight),
10.Reported lactating, pregnant or wishing to become pregnant during the study,
11.Alcohol intake > 210 g per wk for women and > 280 g per wk for men, and
12.Inability or unwillingness to consume foods/beverages provided.
13.Unwillingness to stop the use of supplements 24 hours prior to the testing day.
14.Have any health conditions that would affect food metabolism including the following: food allergies, kidney disease, liver disease and/or gastrointestinal diseases (e.g Irritable bowel syndrome, celiac disease, peptic ulcers)
15.Unable or unwilling to chew gum for 2 hours
16.Unwilling to give up the use of mouth wash while partaking in the study
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
The treatment order for eligible individuals will be randomly assigned using computer generated random numbers. The treatment order allocation will be sealed in numbered envelopes. The envelopes will be used for randomisation by opening an envelope, in consecutive order, as participants are entered in the study. The envelopes will be held by an independent person within the University of Western Australia. The study coordinator will contact the independent person to obtain the next available envelope once an individual is deemed eligible. The envelope will be opened and the code will be recorded.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer-generated random numbers using Microsoft Excel
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/08/2010
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Actual
2/08/2010
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Date of last participant enrolment
Anticipated
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Actual
20/08/2010
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
30
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
258136
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Government body
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Name [1]
258136
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NHMRC
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Address [1]
258136
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National Health and Medical Research Council
GPO Box 1421
Canberra
ACT 2601
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Country [1]
258136
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Australia
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Funding source category [2]
258137
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Commercial sector/Industry
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Name [2]
258137
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The Wrigley Company
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Address [2]
258137
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410 North Michigan Avenue
Chicago, Illinois 60611
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Country [2]
258137
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United States of America
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Primary sponsor type
University
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Name
University of Western Australia
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Address
The University of Western Australia
35 Stirling Highway
Crawley
WA 6009
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Country
Australia
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Secondary sponsor category [1]
257306
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None
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Name [1]
257306
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Address [1]
257306
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Country [1]
257306
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
260116
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University of Western Australia Human Research Ethics Committee
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Ethics committee address [1]
260116
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The University of Western Australia 35 Stirling Highway Crawley WA 6009
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Ethics committee country [1]
260116
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Australia
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Date submitted for ethics approval [1]
260116
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Approval date [1]
260116
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16/06/2010
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Ethics approval number [1]
260116
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RA/4/1/4258
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Summary
Brief summary
This project aims to investigate if chewing gum will increase circulating nitrite and nitric oxide and if these effects are associated with cognitive and vascular benefits.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Jonathan Hodgson
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Address
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University of Western Australia
GPO Box X2213 Perth WA 6847
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Country
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Australia
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Phone
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+61 8 9224 0267
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Catherine Bondonno
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Address
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University of Western Australia
GPO Box X2213 Perth WA 6847
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Country
15199
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Australia
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Phone
15199
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+61 8 9224 0342
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Fax
15199
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Email
15199
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[email protected]
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Contact person for scientific queries
Name
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Catherine Bondonno
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Address
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University of Western Australia
GPO Box X2213 Perth WA 6847
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Country
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Australia
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Phone
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+61 8 9224 0342
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Fax
6127
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Email
6127
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Effects of Chewing Gum on Nitric Oxide Metabolism, Markers of Cardiovascular Health and Neurocognitive Performance after a Nitrate-Rich Meal.
2022
https://dx.doi.org/10.1080/07315724.2020.1869119
N.B. These documents automatically identified may not have been verified by the study sponsor.
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