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Completed

NCT Number: NCT04037943

NUTS for the Prevention of Cardiovascular Disease in Chinese Adults

This study evaluates the feasibility of walnuts supplementation among population of high CVD risks over a period of 6 months. 70 participants will be controls receiving non-edible gifts. 70 participants will be given 30 grams of walnuts everyday and 70 participants will be given 60 grams of walnuts a day.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yi Zhao

Yinchuan, Ningxia, 750004, China

About this study

Increased consumption of nuts improves the levels of lipid risk factors associated with cardiovascular disease and consistently relates to lower risk of cardiovascular disease (CVD) in prospective cohort studies. The estimates of health effects and potential population benefits of increased consumption of nuts are based mostly on observational data and there remains considerable uncertainty about whether higher intake of nuts will actually reduce cardiovascular outcomes. To address this uncertainty will require a well-conducted, adequately powered, large-scale, randomised control trial that tests the causal relationship between nut intake and the risk of cardiovascular diseases.

We hereby designed a 6-month walnut supplementation trial in a rural area of China with high rates of CVD, to obtain data to support and help to refine the design of a future long-term large RCT testing the effect of nut supplementation on CVD risk. The main objectives of the current trial are to assess the acceptability and adherence to two different doses of walnut supplementation (30 and 60 grams per day). The exploratory objectives are to determine the effects of walnut supplementation on cardiovascular risk factors including blood lipids, fasting glucose, and body weight.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A history of CVD, defined on the basis of a prior hospitalisation for a myocardial infarction or stroke, unstable angina, coronary artery bypass graft, percutaneous coronary intervention (with or without stenting), peripheral revascularization (angioplasty or surgery), symptomatic with documented hemodynamically-significant carotid or peripheral vascular disease, or amputation secondary to vascular disease, OR
  • Male aged >60 years, or female aged>65 years, AND

With at least two of the following risk factors:

  • Type 2 diabetes requiring treatment with at least two oral anti-hyperglycaemic agents and/or insulin
  • Systolic blood pressure > 140 mmHg while on one or more antihypertensive agents
  • Current daily smoking
  • Dyslipidaemia defined as HDL-cholesterol<1.0mmol/L or LDL-cholesterol>6.0mmol/L
  • Micro or macro albuminuria

Exclusion criteria

  • Allergic to nuts (history of food allergy with hypersensitivity to any of the components of nuts)
  • Other serious medical condition that prevents nut consumption (e.g. digestive disease with fat intolerance)
  • Any medical condition thought to limit survival to less than 1 year
  • Difficulty with consuming nuts (e.g. dental health issues that prevent chewing walnuts)
  • Unwilling to consume nuts

Treatment and study plan

Walnuts 30 grams

Dietary Supplement

Roasted walnuts without salt or sugar.

Walnuts 60 grams

Dietary Supplement

Roasted walnuts without salt or sugar.

Primary outcomes

  1. Post-intervention differences in blood plasma alpha linolenic acid between groups

    Time frame: From baseline to 6 months

    Blood plasma alpha linolenic acid will be measured at baseline and 6 months (end of trial).

Secondary outcomes

  1. Post-intervention differences in estimated dietary nuts intake from 24h dietary recall between groups

    Time frame: From baseline to 6 months

    Using 24 hour dietary recall to estimate dietary nuts intake at baseline and 6 months (end of trial).

  2. Differences in adherence and acceptability of walnuts between the high and low dose groups

    Time frame: From 2 week, 12 weeks to 6 months

    The adherence and acceptability of the supplement walnuts assessed by questionnaires conducted in the two intervention groups.

Other outcomes

  1. Post-intervention differences in plasma total triglycerides between groups

    Time frame: From baseline to 6 months

    Plasma total triglycerides (mg/dL) will be measured at baseline and 6 months.

  2. Post-intervention differences in plasma total cholesterol between groups

    Time frame: From baseline to 6 months

    Plasma total cholesterol (mg/dL) will be measured at baseline and 6 months.

  3. Post-intervention differences in plasma HDL- cholesterol between groups

    Time frame: From baseline to 6 months

    Plasma HDL- cholesterol (mg/dL) will be measured at baseline and 6 months.

  4. Post-intervention differences in plasma LDL- cholesterol between groups

    Time frame: From baseline to 6 months

    Plasma LDL- cholesterol (mg/dL) will be measured at baseline and 6 months.

  5. Post-intervention differences in blood glucose between groups

    Time frame: From baseline to 6 months

    Blood glucose will be measured at baseline and 6 months.

  6. Post-intervention differences in body weight between groups

    Time frame: From baseline to 6 months

    All participants' body weight will be measured at baseline and 6 months (end of trial) in kilograms.

Sponsors and collaborators

Lead sponsor

The George Institute for Global Health, China

Other

Collaborators

  • Ningxia Medical University

Registry information

Official study title

NUTS for the Prevention of Cardiovascular Disease in Chinese Adults : a Randomized Controlled Trial (NUTS)

Acronym: NUTS

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
Jul 30, 2019
Registry last updated
Aug 9, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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