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Effects of Dietary Nitrate From Vegetable/Fruit Juice on Cerebral Blood Flow Parameters

Effects of Dietary Nitrate From Vegetable/Fruit Juice on Cerebral Blood Flow Parameters

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01169662
Enrollment
40
Registered
2010-07-26
Start date
2010-02-28
Completion date
2010-07-31
Last updated
2010-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebrovascular Circulation, Cognitive Impairment

Brief summary

Nitrate provides the body with an alternative source of Nitric Oxide which plays a large role in promoting blood flow and reducing blood pressure. Nitrate supplementation with vegetable/fruit juice has recently been shown to reduce blood pressure and reduce energy expenditure during low intensity exercise. Such findings combined with the previously known biological effects of nitric oxide would suggest that nitrate supplementation would also impact on blood flow. The aim of this study is to examine the effects of dietary nitrate supplementation via vegetable/fruit juice drink on cerebral (brain) blood flow (using Near Infrared Spectroscopy).

Interventions

DIETARY_SUPPLEMENTVegetable/fruit juice

450ml active juice, 45ml no added sugar fruit squash (for flavour)

DIETARY_SUPPLEMENTPlacebo juice

50 ml No Added Sugar fruit squash, 45 ml Pressed Apple Juice, 405ml with water.

Sponsors

Northumbria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy young (18-35 years) male and female adults, not vulnerable.

Exclusion criteria

* smoke or consume any tobacco products (even occasionally) * not proficient in English * pregnant (or are seeking to become) * currently taking recreational, over the counter/prescription medication (excluding the contraceptive pill), and/or dietary/herbal supplements. * any food allergies or sensitivities that are relevant to the study * history of/current head trauma, learning difficulties, ADHD, dyslexia, migraines or any gastric problems.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline cerebral blood flowFrom baseline to 2.5 hours post-doseNear infrared spectroscopy monitoring of cerebral blood flow in the frontal cortex during demanding tasks. Monitored from baseline, through 90 minutes of drink absorption and 60 minutes of cognitive task performance.
Change from baseline cognitive function90 minutes post-dosePerformance of the cognitive demand battery (CDB), which assesses aspects of psychomotor speed, working memory and executive function. The CDB involves 6 repetitions of the following tasks: serial three subtractions (2 mins); serial seven subtractions (2 mins); Rapid Visual Information Processing (5 mins) and a subjective rating of mental fatigue
Change from baseline mood2.5 hours post-doseBond-Lader visual analogue mood scales assessing the mood factors 'alert'; 'calm'; and 'content'

Secondary

MeasureTime frameDescription
Change from baseline blood pressure, heart rate and venous nitrate and nitrite levels2.5 hours post-doseDiastolic and systolic blood pressure and heart rate monitored after completion of cognitive tasks to assess peripheral blood flow effects. Plasma nitrate and nitrite levels assessed at 2.5 hours post-dose.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026