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Completed

NCT Number: NCT02840357

Impact of Purple Wheat Consumption on Markers of Inflammation and Oxidative Stress in Adults.

The main purpose of this study is to determine the effect of consumption of purple wheat anthocyanin-rich products for eight weeks by human participants with an elevated level of chronic inflammation, on oxidative stress and inflammatory responses as measured by select plasma biomarkers.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Human Nutraceutical Research Unit, University of Guelph

Guelph, Ontario, N1G 2W1, Canada

About this study

This study will investigate the effect of daily consumption of purple wheat bran-enriched wholegrain convenience bars, for 8 weeks on inflammation and oxidative stress biomarkers and plasma antioxidant capacity. This study is a randomized, parallel arm study with 20 men and 20 women who will adhere to a low anthocyanin and low phenolic aid diet for the duration of the study. The participants will be randomly divided into two groups, using stratification for matching sex and screening hs-CRP level to be equally distributed in each group, and assigned to either the treatment group or control group. Both group will have a 10 day diet run-in period where consumption of foods rich in anthocyanins and phenolic acids will be limited. Both groups will consume 4 servings of wheat products per day for 8 weeks and will replace 4 grain servings from their typical daily intake with the study treatment products. Fasting blood samples will be collected during three study visits, including baseline, for the analysis of inflammatory and oxidative stress biomarkers and plasma antioxidant capacity. The plasma metabolites of anthocyanins and phenolic acids will also be determined.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • BMI ≥ 25 kg/m2 and/or Waist circumference ≥102 cm (men) and ≥88 cm (women)
  • hs-CRP: ≥ 1.0 mg/L at time of screening
  • Stable (>3 months) and consistent use of all prescribed medications and/or supplements
  • Non- to moderate alcohol consumer (i.e. less than 5 drinks per sitting and no more than 14 per week)
  • Not taking any antibiotics within the last 3 months, or planning to take antibiotics within the next 6 months

Exclusion criteria

  • Pregnant or breastfeeding females
  • Lifetime history of any acute medical event, including but not limited to, heart attack or stroke
  • Occasional or intermittent smoker (includes but not limited to tobacco and cannabis)
  • Consistent smoker of <1 year
  • Recent diagnosis (within 6 months) of a serious medical condition, including but not limited to, cancer, diabetes, heart disease or hepatitis
  • Recent history (within 6 months) of a clinically significant psychiatric disorder, other than mild depression
  • Any disorder of the gastrointestinal system or food intolerances, including but not limited to, inflammatory bowel disease or Celiac disease
  • Any food allergies or any life-threatening allergies, food or otherwise
  • Regular recreational drug use of more than once per week, including but not limited to cannabis, magic mushrooms, ecstasy etc
  • Difficulty providing blood samples

Treatment and study plan

Purple Wheat Convenience Bars

Other

Whole grain convenience bars manufactured with purple wheat

Control Wheat Convenience Bars

Other

Whole grain convenience bars manufactured with ordinary wheat

Primary outcomes

  1. Serum concentration of inflammatory biomarker (hs-CRP)

    Time frame: Fasting (0 hours)

Secondary outcomes

  1. Plasma concentration of lipids

    Time frame: Fasting (0 hours)

  2. Plasma concentration of inflammatory biomarkers

    Time frame: Fasting (0 hours)

  3. Plasma concentration of total antioxidant capacity

    Time frame: Fasting (0 hours)

  4. Plasma concentrations of anthocyanin metabolites and phenolic acids

    Time frame: Fasting (0 hours)

Sponsors and collaborators

Lead sponsor

University of Guelph

Other

Registry information

Official study title

The Purple Wheat Intervention Study: Impact of Purple Wheat Consumption on Markers of Inflammation and Oxidative Stress in Adults.

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jul 21, 2016
Registry last updated
Apr 2, 2018

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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