Effect of Oat Beta Glucan in Managing Blood Pressure

Elevated Blood Pressure Clinical Trial

Official title:

Effect of Oat Beta Glucan in Managing Blood Pressure: a Randomized Cross-over Pilot Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05029427
• Other study ID #: HS24522(B2020:127)
• Status: Completed
• Phase: N/A
• Start date: November 28, 2021
• Est. completion date: December 23, 2022

Study information

• Verified date: January 2023
• Source: University of Manitoba
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Completed
• Enrollment: 23
• Est. completion date: December 23, 2022
• Est. primary completion date: December 14, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Elevated Blood Pressure
• Hypertension

Intervention

Other:
• High molecular weight ß-glucan oat cookies
Two cookies that contains 4g beta glucan made from oats will be consumed per day.
• Control wheat based cookies
Two cookies that made from cream of wheat without beta glucan will be consumed per day.

Locations

Country	Name	City	State
Canada	Chronic Disease Innovation Centre, Seven Oaks Hospital	Winnipeg	Manitoba

Sponsors (2)

Lead Sponsor	Collaborator
University of Manitoba	Agriculture and Agri-Food Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Dietary fibre by 24 hour recall	Food recalls will be collected through Automated Self-Administered 24-hour dietary assessment tool and analyzed for consumption of dietary fibre	Day 1, 2, and 3 and day 26, 27, and 28 of each study period
Primary	Mean systolic blood pressure	The mean systolic blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine	Day 1 to 3 and day 26-28 of each study period
Secondary	Body weight	Body weight will be measured in kg to the nearest 0.1 kg using a digital scale	Day 1 and day 28 of each study period
Secondary	Waist circumference	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	Day 1 and day 28 of each study period
Secondary	Mean diastolic blood pressure	The mean diastolic blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine	Day 1, 2, and 3 and day 26, 27, and 28 of each study period
Secondary	Mean arterial blood pressure	The mean arterial blood pressure will be measured for 24 hours for 3 consecutive days with an ambulatory blood pressure machine	Day 1, 2, and 3 and day 26, 27, and 28 of each study period