Effect of Oat Beta Glucan in Managing Blood Pressure
- Conditions
- Elevated Blood Pressure
- Interventions
- Other: High molecular weight β-glucan oat cookiesOther: Control wheat based cookies
- Registration Number
- NCT05029427
- Lead Sponsor
- University of Manitoba
- Brief Summary
This is a randomized, double-blinded, cross-over pilot study comparing the effects of ingesting oats containing high molecular weight β-glucan in reducing blood pressure.
- Detailed Description
The pilot study will consist of 2 study periods: one treatment period and one control period. The treatment period will provide food products made from oats containing a total of 4 grams per day high molecular weight (HMW) oat β-glucan, whereas, the control period will provide food products made primarily from wheat with no β-glucan. The study will be located at the Chronic Disease Innovation Centre in Seven Oaks General Hospital, Winnipeg, Canada.
The primary objective of this study is to investigate the effect of ingestion of HMW oat β-glucan on ambulatory blood pressure. Participants will be asked to wear an ambulatory blood pressure monitor for 24 hours per day for 3 consecutive days at the beginning and end of each treatment period. This device automatically measures blood pressure every 15-30 minutes during the day and 30 to 60 minutes during the evening.
The study has been designed to be conducted virtually. Participants will consent to receive both treatment and control over two 4-week periods online. The participants will be randomized to different orders of treatment, with a 4 week wash out period in between.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 23
- Participant is willing and able to give informed consent for participation in the trial
- Generally healthy male and non-pregnant/lactating female, between the ages of 40-75
- When measured by the ambulatory blood pressure monitor, average systolic blood pressure (between 120 and 150mm Hg) and diastolic blood pressure (between 75 and 100mm Hg)
- Willing to comply with protocol requirements
- Willing to maintain their current weight and activity level throughout the study
- Body mass index 18.5-35kg/m2
- Female participant who is pregnant, lactating or planning pregnancy during the course of the trial
- Body mass index ≤ 18.4 and ≥ 35.1 kg/m2
- If there is a history of a secondary cause of hypertension
- Ambulatory blood pressure monitor, systolic blood pressure >150mm Hg or <120mm Hg, diastolic pressure >100mm Hg or <75 mm Hg
- Use of medications containing pseudoephedrine or other vasoconstricting agents
- Antihypertensive drug treatment, regular high dose nonsteroidal anti-inflammatory drugs (NSAID) treatment and the use of cyclosporine or tacrolimus
- Cardiovascular disease including stroke, congestive heart failure, myocardial infarction, unstable angina pectoris, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, temporal ischemic attack within six months prior to screening
- Not willing to maintain their regular physical activity level throughout the intervention
- Use of omega-3 fatty acid, herbal supplements or weight loss drugs
- Diagnosis of diabetes type 1 or type 2
- Scheduled elective surgery or other procedures requiring general anaesthesia during the trial
- Any other significant disease or disorder which, in the opinion of the Investigator or study physician, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial
- Recent history (within 6 month of screening) or current consumption of >14 drinks per week, (1 drink = 12oz of beer, 5oz of wine or 1.5oz distilled spirits)
- Body weight change over 3.5kg for the past 3 months
- Smokers and tobacco/snuff/nicotine users
- Allergy to oats, wheat, peanut, apple, cherry, blueberry, quinoa, egg white, margarine and vanilla extract.
- Regular consumption of supplements which may influence blood pressure/consumption of food supplements targeted to blood pressure lowering within 30 days before and during the study
- Participants who have participated in another research trial involving an investigational product in the past 12 weeks
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Study period 1: β-glucan Oat ; Study period 2: Wheat Control wheat based cookies For the first period, the participant will receive food products made from oats containing a total of 4 grams per day HMW oat β-glucan. For the second period, the participant will receive food products made from wheat. Study period 1: Wheat ; Study period 2: β-glucan Oat High molecular weight β-glucan oat cookies For the first period, the participant will receive food products made from wheat. For the second period, the participant will receive food products made from oats containing a total of 4 grams per day HMW oat β-glucan. Study period 1: Wheat ; Study period 2: β-glucan Oat Control wheat based cookies For the first period, the participant will receive food products made from wheat. For the second period, the participant will receive food products made from oats containing a total of 4 grams per day HMW oat β-glucan. Study period 1: β-glucan Oat ; Study period 2: Wheat High molecular weight β-glucan oat cookies For the first period, the participant will receive food products made from oats containing a total of 4 grams per day HMW oat β-glucan. For the second period, the participant will receive food products made from wheat.
- Primary Outcome Measures
Name Time Method Mean systolic blood pressure Day 1 to 3 and day 26-28 of each study period The mean systolic blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine
- Secondary Outcome Measures
Name Time Method Waist circumference Day 1 and day 28 of each study period Waist circumference in cm will be measured in triplicate, to the nearest 0.1 cm at the umbilicus, between the last rib and iliac crest using a fibreglass tape
Mean diastolic blood pressure Day 1, 2, and 3 and day 26, 27, and 28 of each study period The mean diastolic blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine
Mean arterial blood pressure Day 1, 2, and 3 and day 26, 27, and 28 of each study period The mean arterial blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine
Body weight Day 1 and day 28 of each study period Body weight will be measured in kg to the nearest 0.1 kg using a digital scale
Trial Locations
- Locations (1)
Chronic Disease Innovation Centre, Seven Oaks Hospital
🇨🇦Winnipeg, Manitoba, Canada