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Nuts and Extra Virgin Olive Oil Pilot Study

Primary Purpose

Hypertension

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Walnuts
Extra Virgin Olive Oil
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hypertension

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Being treated for hypertension-defined by being prescribed at least one hypertension medication; willing to comply with study visits, as outlined in the protocol; able to read and speak English; no allergies or hypersensitivities to olive oil or nuts; ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Plans to move from the study area in the next 8 weeks; dementia that is medically documented or suspected; homebound for medical reasons; cancer diagnosis and/or treatment in the last 3 years.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Intervention

    Arm Description

    All participants will receive an 8-week supply of walnuts and Extra Virgin Olive Oil (EVOO). Study supplements will consist of 28 gm of walnuts and 32 gm of EVOO per day. Participants will be instructed how to consume the proper amount of walnuts and EVOO and to report their consumption using a compliance diary. The walnuts are pre-packaged in daily servings (one 28 g packet per day) and measuring spoons will be provided with the olive oil to assist participants in consuming it appropriately. Participants will also receive recipes and other written information that will assist them in incorporating both the nuts and olive oil into their existing dietary patterns.

    Outcomes

    Primary Outcome Measures

    Retention of study participants
    To estimate retention (measured by number attending the 8 week closeout visit) of men and women being treated for hypertension in the 8 week study.
    Adherence to consuming walnuts and EVOO
    To assess adherence to consuming the nut and oil supplements (measured by daily diary of supplement intake) over the course of the study.

    Secondary Outcome Measures

    Blood pressure
    To estimate the variability of blood pressure in men and women participating in the study
    Weight
    To estimate the variability of weight in men and women participating in the study
    HDL cholesterol
    To estimate the variability of HDL cholesterol in men and women participating in the study
    Adverse events
    To document the types and the rates of adverse events associated with the supplements.

    Full Information

    First Posted
    July 11, 2016
    Last Updated
    July 30, 2018
    Sponsor
    Wake Forest University Health Sciences
    Collaborators
    California Walnut Growers Association, C.H.O. American, Natural and Organic Olive Oil Producer Association
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02831803
    Brief Title
    Nuts and Extra Virgin Olive Oil Pilot Study
    Official Title
    A Pilot Study to Evaluate the Feasibility of Walnut and Extra Virgin Olive Oil Supplementation in Older Adults Being Treated for Hypertension
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2014 (undefined)
    Primary Completion Date
    December 2014 (Actual)
    Study Completion Date
    January 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Wake Forest University Health Sciences
    Collaborators
    California Walnut Growers Association, C.H.O. American, Natural and Organic Olive Oil Producer Association

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study is designed to test the feasibility of asking older adults with high blood pressure to supplement their daily diets with walnuts and extra-virgin olive oil.
    Detailed Description
    Even though cardiovascular disease (CVD) continues to be the leading cause of death in the United States, Americans have yet to widely adopt evidence-based dietary modifications necessary to reduce CVD risk factors. Encouraging evidence from the Prevención con Dieta Mediterránea (PREDIMED) trial indicates that adding olive oil and nuts to the diets of older adults in Spain substantially impacted CVD risk factors and events. A large trial testing EVOO and nuts in a U.S. population is needed to determine if supplementing with EVOO and nuts can reduce risk of cardiovascular events and mortality in adults living in the U.S. Prior to launching a large trial, it is important to assess whether adults 55 and older would be interested in participating in a supplementation trial such as PREDIMED. Additionally, it is important to assess if they are willing to consume the nuts and EVOO and attend study related-data collection visits.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    27 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    All participants will receive an 8-week supply of walnuts and Extra Virgin Olive Oil (EVOO). Study supplements will consist of 28 gm of walnuts and 32 gm of EVOO per day. Participants will be instructed how to consume the proper amount of walnuts and EVOO and to report their consumption using a compliance diary. The walnuts are pre-packaged in daily servings (one 28 g packet per day) and measuring spoons will be provided with the olive oil to assist participants in consuming it appropriately. Participants will also receive recipes and other written information that will assist them in incorporating both the nuts and olive oil into their existing dietary patterns.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Walnuts
    Intervention Description
    28 gm/day in single-serve package
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Extra Virgin Olive Oil
    Intervention Description
    32 gm/day provided in 3, 34 ounce bottles
    Primary Outcome Measure Information:
    Title
    Retention of study participants
    Description
    To estimate retention (measured by number attending the 8 week closeout visit) of men and women being treated for hypertension in the 8 week study.
    Time Frame
    8 weeks
    Title
    Adherence to consuming walnuts and EVOO
    Description
    To assess adherence to consuming the nut and oil supplements (measured by daily diary of supplement intake) over the course of the study.
    Time Frame
    8 weeks
    Secondary Outcome Measure Information:
    Title
    Blood pressure
    Description
    To estimate the variability of blood pressure in men and women participating in the study
    Time Frame
    8 weeks
    Title
    Weight
    Description
    To estimate the variability of weight in men and women participating in the study
    Time Frame
    8 weeks
    Title
    HDL cholesterol
    Description
    To estimate the variability of HDL cholesterol in men and women participating in the study
    Time Frame
    8 weeks
    Title
    Adverse events
    Description
    To document the types and the rates of adverse events associated with the supplements.
    Time Frame
    8 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    55 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Being treated for hypertension-defined by being prescribed at least one hypertension medication; willing to comply with study visits, as outlined in the protocol; able to read and speak English; no allergies or hypersensitivities to olive oil or nuts; ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: Plans to move from the study area in the next 8 weeks; dementia that is medically documented or suspected; homebound for medical reasons; cancer diagnosis and/or treatment in the last 3 years.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mara Z Vitolins, DrPH MPH RDN
    Organizational Affiliation
    Wake Forest University Health Sciences
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Nuts and Extra Virgin Olive Oil Pilot Study

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