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Olive Leaf Extract as Part of a Healthy Lifestyle in the Reduction of Blood Pressure

Primary Purpose

Pre Hypertension

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Olive leaf extract
Placebo
Sponsored by
University of Reading
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pre Hypertension

Eligibility Criteria

25 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Men and women
  • 25-70y
  • BMI >25kg/m2
  • Not having suffered a myocardial infarction/stroke in the past 12 months
  • Not diabetic (diagnosed or fasting glucose > 7 mmol/l) or suffer from other endocrine disorders
  • Not suffering from renal or bowel disease or have a history of cholestatic liver or pancreatitis
  • Not on drug treatment for hyperlipidaemia, hypertension, inflammation or hypercoagulation
  • No history of alcohol misuse
  • Not planning or on a weight reducing regime
  • Not taking any fish oil, fatty acid or vitamin and mineral supplements
  • Non smokers

Exclusion Criteria:

  • Use of antibiotics within the previous 6 months
  • History of alcohol or drug abuse
  • Intake of any experimental drug within 4 weeks of the start of the study
  • Excessive alcohol consumption (more than 21 units/wk male, 15 units/wk female)
  • Females who are breast-feeding, may be pregnant, or of child-bearing potential and not using effective contraceptive precautions
  • Have had recently (in the last 5 years) major surgery, which might limit participation in, or completion of, the study.
  • On drug treatment for high blood fats, high blood pressure and blood clotting.
  • Physical or mental diseases that are likely to limit participation or completion of the study

Sites / Locations

  • Hugh Sinclair Unit of Human Nutrition

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Placebo Comparator

Active Comparator

Arm Label

Placebo control

Olive leaf extract

Physical activity

Physical activity and olive leaf extract

Arm Description

2 capsules of 350 mg maltodextrin to be consumed daily for 12 weeks

2 capsules of 350 mg olive leaf extract equivalent 132 mg of oleuropein in olive leaf extract to be consumed daily for 12 weeks

2 capsules of 350 mg maltodextrin to be consumed daily combined with gradually increase physical activity levels over 12 weeks

2 capsules of 350 mg olive leaf extract equivalent 132 mg of oleuropein in olive leaf extract to be consumed daily combined with gradually increase physical activity levels over 12 weeks

Outcomes

Primary Outcome Measures

Blood pressure measured via 24 hour ambulatory blood pressure monitors
measured using the ScanMed Oscillometric Ambulatory blood pressure deviceVolunteers will be asked to wear the device which will be programmed to record BP measurements every 30 minutes during the day (7am-10pm) and every hour by night (10pm-7am)

Secondary Outcome Measures

Average plasma glucose concentration
a measure of chronic blood sugar control) by measuring of glycated haemoglobin (HbA1c)
Vascular function assessed by pulse wave velocity (PWV)
Plasma biomarkers of endothelial function including nitric oxide, vascular cell adhesion molecule (VCAM), Inter-Cellular Adhesion Molecule (ICAM), E-selectin, von Willebrand factor
Fasting lipid profile including measures of total, low density lipoprotein (LDL) and high density lipoprotein (HDL) cholesterol, triglycerides and non-esterified fatty acids
Indices of insulin resistance derived from fasted measures of glucose, insulin and non-esterified fatty acids (revised QUICKI statistical analysis)
Haemostatic factors including Plasminogen activator inhibitor-1 (PAI-1)
Inflammatory biomarkers including the acute phase proteins, C-reactive protein (CRP), tumour necrosis factor alpha (TNFα), Interleukin-6 (IL6)

Full Information

First Posted
April 10, 2015
Last Updated
May 27, 2016
Sponsor
University of Reading
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1. Study Identification

Unique Protocol Identification Number
NCT02421835
Brief Title
Olive Leaf Extract as Part of a Healthy Lifestyle in the Reduction of Blood Pressure
Official Title
Olive Leaf Extract as Part of a Healthy Lifestyle in the Reduction of Blood Pressure
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Reading

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypertension affects about 30% of the United Kingdom population and is causally implicated in the aetiology of renal disease, cardiovascular disease and stroke. Ageing, obesity, a poor diet and low levels of physical activity are all risk factors. Studies have shown that adherence to a Mediterranean diet is protective against hypertension and its associated morbidities; olive oil is believed to be a key beneficially bioactive component of that diet. As a source of lipids olive oil is an unremarkable blend of monounsaturated, polyunsaturated and saturated fatty acids; it is however rich in phenolic compounds, principally oleuropein and hydroxytyrosol, which may be of benefit to health. A recent randomised intervention trial in predominantly hypertensive volunteers showed that adherence to a Mediterranean diet supplemented with extra virgin olive oil, reduced blood pressure and other measures of cardiovascular disease risk. Olive phenolics can be extracted cheaply from the waste products of olive oil manufacture, such as the plant leaf and these are used as dietary supplements. In intervention studies in hypertensive or borderline hypertensive patients, olive leaf extract consumption has been shown to reduce blood pressure. Another intervention with established efficacy for improving blood pressure is to increase physical activity. The 'Start Active, Stay Active', Chief Medical Officers report on physical activity recommends that adults achieve 150 minutes of moderate intensity physical activity per week, while data in that report suggest that fewer than 40% of adult men and 30% of adult women achieve these targets. Adherence to the physical activity guidelines may in fact be much worse in sub-sections of the population at higher risk of hypertension. From a public health perspective, holistic guidelines for the prevention of hypertension, or its early diagnosis and management, based around a healthy diet and lifestyle are preferable to pharmaceutical intervention. Lifestyle interventions are economically favourable and they come with fewer side effects and perhaps wider health benefits than antihypertensive drugs. The aim of the study is to evidence the synergistic benefits of consuming plant (and specifically olive) phenolics alongside achieving the recommended guidelines for physical activity in individuals with elevated blood pressure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre Hypertension

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo control
Arm Type
Placebo Comparator
Arm Description
2 capsules of 350 mg maltodextrin to be consumed daily for 12 weeks
Arm Title
Olive leaf extract
Arm Type
Active Comparator
Arm Description
2 capsules of 350 mg olive leaf extract equivalent 132 mg of oleuropein in olive leaf extract to be consumed daily for 12 weeks
Arm Title
Physical activity
Arm Type
Placebo Comparator
Arm Description
2 capsules of 350 mg maltodextrin to be consumed daily combined with gradually increase physical activity levels over 12 weeks
Arm Title
Physical activity and olive leaf extract
Arm Type
Active Comparator
Arm Description
2 capsules of 350 mg olive leaf extract equivalent 132 mg of oleuropein in olive leaf extract to be consumed daily combined with gradually increase physical activity levels over 12 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Olive leaf extract
Intervention Description
132 mg of oleuropein per day suspended in olive leaf extract 700 mg
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Other Intervention Name(s)
Maltodextrin
Intervention Description
700 mg Maltodextrin per day
Primary Outcome Measure Information:
Title
Blood pressure measured via 24 hour ambulatory blood pressure monitors
Description
measured using the ScanMed Oscillometric Ambulatory blood pressure deviceVolunteers will be asked to wear the device which will be programmed to record BP measurements every 30 minutes during the day (7am-10pm) and every hour by night (10pm-7am)
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Average plasma glucose concentration
Description
a measure of chronic blood sugar control) by measuring of glycated haemoglobin (HbA1c)
Time Frame
12 weeks
Title
Vascular function assessed by pulse wave velocity (PWV)
Time Frame
12 weeks
Title
Plasma biomarkers of endothelial function including nitric oxide, vascular cell adhesion molecule (VCAM), Inter-Cellular Adhesion Molecule (ICAM), E-selectin, von Willebrand factor
Time Frame
12 weeks
Title
Fasting lipid profile including measures of total, low density lipoprotein (LDL) and high density lipoprotein (HDL) cholesterol, triglycerides and non-esterified fatty acids
Time Frame
12 weeks
Title
Indices of insulin resistance derived from fasted measures of glucose, insulin and non-esterified fatty acids (revised QUICKI statistical analysis)
Time Frame
12 weeks
Title
Haemostatic factors including Plasminogen activator inhibitor-1 (PAI-1)
Time Frame
12 weeks
Title
Inflammatory biomarkers including the acute phase proteins, C-reactive protein (CRP), tumour necrosis factor alpha (TNFα), Interleukin-6 (IL6)
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men and women 25-70y BMI >25kg/m2 Not having suffered a myocardial infarction/stroke in the past 12 months Not diabetic (diagnosed or fasting glucose > 7 mmol/l) or suffer from other endocrine disorders Not suffering from renal or bowel disease or have a history of cholestatic liver or pancreatitis Not on drug treatment for hyperlipidaemia, hypertension, inflammation or hypercoagulation No history of alcohol misuse Not planning or on a weight reducing regime Not taking any fish oil, fatty acid or vitamin and mineral supplements Non smokers Exclusion Criteria: Use of antibiotics within the previous 6 months History of alcohol or drug abuse Intake of any experimental drug within 4 weeks of the start of the study Excessive alcohol consumption (more than 21 units/wk male, 15 units/wk female) Females who are breast-feeding, may be pregnant, or of child-bearing potential and not using effective contraceptive precautions Have had recently (in the last 5 years) major surgery, which might limit participation in, or completion of, the study. On drug treatment for high blood fats, high blood pressure and blood clotting. Physical or mental diseases that are likely to limit participation or completion of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Commane, PhD
Organizational Affiliation
Reading University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hugh Sinclair Unit of Human Nutrition
City
Reading
State/Province
Berkshire
ZIP/Postal Code
RG6 6AP
Country
United Kingdom

12. IPD Sharing Statement

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