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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02391779
Other study ID # FSL132
Secondary ID
Status Completed
Phase Phase 2
First received February 28, 2015
Last updated January 8, 2018
Start date May 2015
Est. completion date July 2017

Study information

Verified date January 2018
Source University of Saskatchewan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Current recommendations today suggest that use of therapeutic lifestyle changes, such as supplementation with specific dietary components and moderate exercise, are appropriate interventions for individuals with borderline high blood pressure. Dietary intervention with natural products, such as flaxseed, is associated with decreased prevalence of cardiovascular disease (Adolphe 2010). Lignans are the active compounds in flaxseed believed to mediate the cardiovascular health benefits following flaxseed consumption (Peterson 2010). Clinical trials indicate benefit of Flax Lignan Enriched Complex (FLC) (BeneFlax® from Archer Daniels Midland, a natural product derived from flaxseed composed of 34-38% lignan) for reducing blood cholesterol and glucose (Pan 2007; Zhang 2008) and blood pressure (Cornish 2009). Furthermore, a recent study in atherosclerosis patients showed significant clinical benefit of flaxseed meal for reducing blood pressure (Rodriguez-Leyva 2013). As a therapeutic lifestyle change that could prevent a need to introduce drug therapy in elderly patients, the effectiveness of FLC supplementation alone or in combination with moderate exercise merits investigation.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria:

- High normal blood pressure (130/85 - 139/89) or stage I hypertension (140/90 - 150/90)

- Ability to follow simple instructions

Exclusion Criteria:

- Age below 60 years.

- Individuals living in long term care homes.

- Individuals unable to walk for 30 minutes.

- Unstable diabetes, or diabetics taking insulin (note: eligible diabetic participants will undergo additional testing during the study ).

- Current cancer or diagnosed with cancer in the past 2 years.

- Significant liver or other gastrointestinal disorder including inflammatory bowel disease. (While constipation is the most common gastrointestinal problem in the elderly, it would not be a contraindication)

- Significant kidney disorder.

- Have taken oral antibiotics in the past three months

- Unstable or severe cardiac disease, recent myocardial infarction, or stroke (either in past 6 months or significantly affecting physical mobility).

- Unstable other medical disease including, but not limited to, pulmonary disorder, epilepsy and genitourinary disorder.

- Migraine with aura within the last year (as this is a risk factor for stroke).

- Current diagnosis of a bleeding condition, or at risk of bleeding.

- Significant immune-compromise.

- Current use of hormone replacement therapy (except thyroid).

- Current use of blood pressure medications and/or diuretics

- Current use of flax seed supplement

- Participation in any other clinical trial with an investigational agent within one month prior to randomization.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
BeneFlax®
Daily ingestion of 600 mg SDG/day in 1.6 g SDG-enhanced flax lignan (BeneFlax®) with walking training or flexibility training
Behavioral:
Walking training
30-60 minutes walking training, 5 days/week.
Flexibility training
5 days/week; e.g. stretching training at home
Dietary Supplement:
Placebo (Whey Protein)
0.6 g/day (an amount equal in volume to BeneFlax®) with walking training or flexibility training
Behavioral:
Dash Eating Plan
Dietary Approaches to Stop Hypertension (DASH), a balanced eating plan - all participants in all treatment arms will be encouraged to adopt a DASH eating plan.

Locations

Country Name City State
Canada College of Pharmacy, University of Saskatchewan Saskatoon Saskatchewan

Sponsors (1)

Lead Sponsor Collaborator
University of Saskatchewan

Country where clinical trial is conducted

Canada, 

References & Publications (6)

Adolphe JL, Whiting SJ, Juurlink BH, Thorpe LU, Alcorn J. Health effects with consumption of the flax lignan secoisolariciresinol diglucoside. Br J Nutr. 2010 Apr;103(7):929-38. doi: 10.1017/S0007114509992753. Epub 2009 Dec 15. Review. — View Citation

Cornish SM, Chilibeck PD, Paus-Jennsen L, Biem HJ, Khozani T, Senanayake V, Vatanparast H, Little JP, Whiting SJ, Pahwa P. A randomized controlled trial of the effects of flaxseed lignan complex on metabolic syndrome composite score and bone mineral in older adults. Appl Physiol Nutr Metab. 2009 Apr;34(2):89-98. doi: 10.1139/H08-142. — View Citation

Pan A, Sun J, Chen Y, Ye X, Li H, Yu Z, Wang Y, Gu W, Zhang X, Chen X, Demark-Wahnefried W, Liu Y, Lin X. Effects of a flaxseed-derived lignan supplement in type 2 diabetic patients: a randomized, double-blind, cross-over trial. PLoS One. 2007 Nov 7;2(11):e1148. — View Citation

Peterson J, Dwyer J, Adlercreutz H, Scalbert A, Jacques P, McCullough ML. Dietary lignans: physiology and potential for cardiovascular disease risk reduction. Nutr Rev. 2010 Oct;68(10):571-603. doi: 10.1111/j.1753-4887.2010.00319.x. Review. — View Citation

Rodriguez-Leyva D, Weighell W, Edel AL, LaVallee R, Dibrov E, Pinneker R, Maddaford TG, Ramjiawan B, Aliani M, Guzman R, Pierce GN. Potent antihypertensive action of dietary flaxseed in hypertensive patients. Hypertension. 2013 Dec;62(6):1081-9. doi: 10.1161/HYPERTENSIONAHA.113.02094. Epub 2013 Oct 14. — View Citation

Zhang W, Wang X, Liu Y, Tian H, Flickinger B, Empie MW, Sun SZ. Dietary flaxseed lignan extract lowers plasma cholesterol and glucose concentrations in hypercholesterolaemic subjects. Br J Nutr. 2008 Jun;99(6):1301-9. Epub 2007 Dec 6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Number of participants with adverse events as a safety measurement Continuously throughout 9 weeks
Other Number of participants with severe non-compliance with the protocol Continuously throughout 9 weeks
Primary Change in 24 h ambulatory systolic blood pressure Reduction in 24 h ambulatory systolic blood pressure at midpoint (week 4) and end (week 8) of the intervention relative to baseline value is the primary outcome of the intervention. Baseline, week 4, and week 8
Secondary Change in body weight Change in body weight at midpoint (week 4) and end (week 8) of the intervention relative to baseline value. Baseline, week 4, and week 8
Secondary Heart rate Baseline
Secondary Glucometer fasting blood glucose Diabetes only; Blood glucose monitored to ensure intervention does not result in hypoglycemia. Baseline
Secondary Change in blood markers of safety and cardiovascular disease risk factors (clinical biochemical panel including fasting glucose, lipids, cholesterol, electrolytes, C-reactive protein) These parameters will be measured individual but reviewed as a composite to confirm safety and any change in cardiovascular disease risk. Baseline, week 4, and week 8
Secondary Blood levels of the flax lignan, secoisolariciresinol diglucoside (SDG), and its metabolites Week 4
Secondary Physical activity assessment tool (PASE) Baseline
Secondary Block Food Frequency Questionnaire Baseline
Secondary Change in Body composition by DXA (Dual-energy X-ray absorptiometry) Change in body composition at midpoint (week 4) and end (week 8) of the intervention relative to baseline value. Baseline, week 4, and week 8
Secondary Heart Rate week 4
Secondary Heart Rate Week 8
Secondary Change in lying and standing blood pressure Change in lying and standing blood pressure at midpoint (week 4) and end (week 8) of the intervention relative to baseline value. Baseline, week 4, and week 8
Secondary Respiratory rate Baseline
Secondary Respiratory rate Week 4
Secondary Respiratory rate Week 8
Secondary Block Food Frequency Questionnaire Week 8
Secondary Blood levels of the flax lignan, secoisolariciresinol diglucoside (SDG), and its metabolites Week 8
Secondary Glucometer fasting blood glucose Diabetes only; Blood glucose monitored to ensure intervention does not result in hypoglycemia. Week 4
Secondary Glucometer fasting blood glucose Diabetes only; Blood glucose monitored to ensure intervention does not result in hypoglycemia. Week 8
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