Supplementation of 500mg Trans-resveratrol Within Hypoxic and Normoxic Conditions, in Healthy Humans.

Objectives: Resveratrol, a non-flavonoid polyphenol, has been found to consistently modulate cerebral blood flow (CBF) following oral supplementation. Although, this has not resulted in subsequent predicted benefits to cognitive performance in young healthy populations. However, it is argued that those who suffer a reduction in CBF and cognition, such as aging populations, may benefit more from resveratrol administration.

Hypothesis: The current investigation aimed to employ a mild hypoxia as an experimental model of aging in a young healthy population, to assess if resveratrol can attenuate the deficits elicited by the reduction in oxygen supply. It was hypothesized resveratrol would module CBF, to provide a more efficient supply of oxygen to overcome any associated decreases to performance caused by the hypoxic model.

Design: This repeated measures, double blind, placebo controlled, balanced design assessed the cognitive and CBF effects of resveratrol in hypoxia (equivalent to ~2000m above sea level) and normoxia (sea level).

Methods: 24 participants arrived fully fasted (except water) for 12 hrs before completing a baseline measure of a cognitive task battery, and taking the treatment for the day. Following a 45 min absorption period, participants completed 3 full repetitions of the cognitive test battery and, if appropriate, the oxygen level was altered. Changes in CBF were measured by near-infrared spectroscopy throughout the full testing session.

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Key information

Conditions

Hypoxia, Brain Brain Diseases Central Nervous System Diseases Hypoxia Nervous System Diseases Pathological Conditions, Signs and Symptoms Signs and Symptoms Signs and Symptoms, Respiratory

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Participants who gave informed consent.
Those who didn't meet any of the exclusion criteria.
Those who took hormonal contraception (e.g.: the pill, coil, implant, etc.) were allow to participate in the current study.

Exclusion criteria

Smokers.
People below 18 or above 35 years old at the time of giving consent
People with Body Mass Index outside of the range 18-35 kg/m2.
People with blood pressure greater than 140/90 HH/mg
People who have been living (for more than 3 months) at an altitude of 2000 m or over within the past 6 months.
People with a history of neurological, vascular or psychiatric illness (excluding depressive illness and anxiety).
People with a current diagnosis of depression and/or anxiety.
Participants with learning difficulties, dyslexia or colour blindness.
Participants with visual impairment that cannot be corrected with glasses or contact lenses.
Participants with frequent migraines that require medication (more than or equal to 1 per month).
Participants with disorders of the blood.
Participants with a heart disorder.
Participants with a respiratory disorder that requires regular medication (Note: asthma sufferers who only take their medication occasionally/as required are eligible for this study).
Participants with diabetes.
Participants with any food intolerances/sensitivities.
Women who are pregnant, or seeking to become pregnant, or are currently lactating.
Participants currently taking any prescription medications.
Participants who have habitually used dietary supplements within the last month (defined as more than 3 consecutive days or 4 days in total).
Participants with 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.
Participants with any health condition that would prevent fulfilment of the study requirements.

Treatment and study plan

Resveratrol

Dietary Supplement

Placebo

Drug

Primary outcomes

Cerebral blood flow

Time frame: 2 hours

Cerebral heamodynamic response (of the prefrontal cortex) at rest and during task performance (all concentration change (μmol / L)).

There are 3 outputs to this (oxygenated, de-oxygenated and total heamoglobin, detailing changes of oxygenation and de-oxygenation in the neural tissue at rest and during task performance.
Cognitive performance

Time frame: 1 hour

Participants completed a number of tasks to measure cognitive domain performance (Episodic Memory, Speed of Attention, & Accuracy of Attention), as part of a 15 minute cognitive battery. Outcomes were measured in accuracy of responses to each task (% correct), reaction time to respond to each task (in milliseconds (ms), and the number of error responses when completing each task.

Sponsors and collaborators

Lead sponsor

Northumbria University

Other

Registry information

Official study title

The Effects of Acute Trans-resveratrol Supplementation on Aspects of Cognitive Function and Cerebral Blood Flow, During Hypoxia and Normoxia, in Healthy, Young Humans.

Important dates

Study start: 2014
Primary completion: 2015
Study completion: 2015
First posted: Apr 4, 2017
Registry last updated: Apr 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed