Yi Zhao
Yinchuan, Ningxia, 750004, China
NCT Number: NCT04037943
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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Interventional
Not applicable
Yinchuan, Ningxia, 750004, China
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
With at least two of the following risk factors:
Exclusion criteria
Roasted walnuts without salt or sugar.
Roasted walnuts without salt or sugar.
Time frame: From baseline to 6 months
Blood plasma alpha linolenic acid will be measured at baseline and 6 months (end of trial).
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).
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.
Time frame: From baseline to 6 months
Plasma total triglycerides (mg/dL) will be measured at baseline and 6 months.
Time frame: From baseline to 6 months
Plasma total cholesterol (mg/dL) will be measured at baseline and 6 months.
Time frame: From baseline to 6 months
Plasma HDL- cholesterol (mg/dL) will be measured at baseline and 6 months.
Time frame: From baseline to 6 months
Plasma LDL- cholesterol (mg/dL) will be measured at baseline and 6 months.
Time frame: From baseline to 6 months
Blood glucose will be measured at baseline and 6 months.
Time frame: From baseline to 6 months
All participants' body weight will be measured at baseline and 6 months (end of trial) in kilograms.
The George Institute for Global Health, China
Other
NUTS for the Prevention of Cardiovascular Disease in Chinese Adults : a Randomized Controlled Trial (NUTS)
Acronym: NUTS
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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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