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| ID | Type | Description | Link |
|---|---|---|---|
| 2025-Dachundou-IRB-25-058-A2 | Other Identifier | WEI CHUAN FOODS CORPORATION |
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Cardiovascular disease is one of the leading causes of death worldwide, and high cholesterol is a major risk factor. Diet is known to play an important role in managing blood lipids. Soy milk is a common plant-based drink rich in protein and isoflavones, which may help lower cholesterol and improve heart health.
This clinical trial will evaluate whether daily consumption of Dachundou No Sugar Added Soymilk can help reduce cholesterol levels in adults with elevated total cholesterol (≥200 mg/dL). A total of 50 participants aged 18-65 will be recruited. Participants will drink two bottles of soymilk per day (375 mL each, total 750 mL) for 8 weeks.
During the study, researchers will measure cholesterol, blood pressure, body weight, waist circumference, and other health indicators. The results will help determine whether Dachundou No Sugar Added Soymilk can improve blood lipid levels and contribute to cardiovascular health.
Cardiovascular disease remains a leading cause of morbidity and mortality worldwide, with dyslipidemia being one of the most important risk factors. Dietary interventions, such as plant-based proteins and bioactive compounds, have been shown to improve lipid profiles and reduce cardiovascular risk. Soy milk is widely consumed in Asia and contains soy protein and isoflavones, which have antioxidant, anti-inflammatory, and lipid-regulating effects.
Previous studies suggest that soy protein may lower total cholesterol and LDL-C through inhibition of HMG-CoA reductase and upregulation of LDL receptor expression, while soy isoflavones may enhance lipid metabolism and endothelial function through estrogen-like actions.
This trial aims to evaluate the lipid-lowering efficacy of Dachundou No Sugar Added Soymilk in adults with fasting total cholesterol ≥200 mg/dL. A total of 50 participants, aged 18-65 years, non-smokers, without alcohol abuse, and otherwise healthy, will be enrolled. All participants will consume two bottles of soymilk per day (375 mL each; total 750 mL) for 8 consecutive weeks.
Assessments will be performed at baseline (week -2 and week 0), during the intervention (week 4 and week 8), and post-intervention (week 10). Measurements include anthropometrics (height, weight, waist circumference, blood pressure), blood biochemistry (lipid profile, glucose, liver and kidney function), oxidative stress (oxidized LDL via TBARS), and lifestyle factors (dietary records and physical activity questionnaires).
The primary outcome is the change in total cholesterol from baseline to week 8. Secondary outcomes include changes in LDL-C, HDL-C, triglycerides, oxidized LDL, liver/kidney function, and anthropometric indices. The findings will provide evidence on whether Dachundou No Sugar Added Soymilk can serve as a dietary intervention to improve blood lipid levels and promote cardiovascular health.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Soymilk Intervention | Experimental | Participants will consume two bottles of Dachundou No Sugar Added Soymilk daily (375 mL each; total 750 mL per day) for 8 consecutive weeks. Assessments will be performed at baseline (week -2 and week 0), during the intervention (week 4 and week 8), and post-intervention (week 10). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dachundou No Sugar Added Soymilk | Dietary Supplement | Participants will consume two bottles of Dachundou No Sugar Added Soymilk daily (375 mL each; total 750 mL per day) for 8 consecutive weeks. The product is packaged in 375 mL cartons and made from non-GMO soybeans, containing approximately 4.2 g of soy protein per 100 mL. The soymilk is unsweetened and stored at 0-7°C. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in total cholesterol (TC) | Serum total cholesterol concentration will be measured using an automated biochemical analyzer to evaluate the lipid-lowering efficacy of Dachundou No Sugar Added Soymilk. | Baseline (week 0) to week 8 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in LDL cholesterol (LDL-C) | LDL-C concentration measured by automated biochemical analyzer. | Baseline to week 8 |
| Change in HDL cholesterol (HDL-C) | HDL-C concentration measured by automated biochemical analyzer. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Taiwan Sport University | Taoyuan | 333325 | Taiwan |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 28338639 | Result | Ramdath DD, Padhi EM, Sarfaraz S, Renwick S, Duncan AM. Beyond the Cholesterol-Lowering Effect of Soy Protein: A Review of the Effects of Dietary Soy and Its Constituents on Risk Factors for Cardiovascular Disease. Nutrients. 2017 Mar 24;9(4):324. doi: 10.3390/nu9040324. |
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Individual participant data (IPD) will not be shared because the trial involves sensitive health-related data collected from human participants. Only aggregated and de-identified summary results will be published in scientific journals and conference presentations.
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| ID | Term |
|---|---|
| D050171 | Dyslipidemias |
| D006937 | Hypercholesterolemia |
| D002318 | Cardiovascular Diseases |
| ID | Term |
|---|---|
| D052439 | Lipid Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D006949 | Hyperlipidemias |
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This is a single-group, open-label interventional study. All participants meeting the eligibility criteria will receive the same intervention: daily supplementation with Dachundou No Sugar Added Soymilk (2 bottles of 375 mL each; total 750 mL/day) for 8 consecutive weeks. No control or placebo group will be included. Outcomes will be assessed at baseline (week -2 and week 0), mid-intervention (week 4), end of intervention (week 8), and follow-up (week 10).
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This study is conducted as an open-label, single-group dietary intervention. No masking is applied to participants, investigators, care providers, or outcome assessors.
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| Baseline to week 8 |
| Change in triglycerides (TG) | Serum triglyceride concentration measured by automated biochemical analyzer. | Baseline to week 8 |
| Change in oxidized LDL (TBARS assay) | Oxidative stress marker (TBARS values in LDL fraction). | Baseline to week 8 |
| Change in body weight (kg) | Weight will be measured using a calibrated digital scale, with participants wearing light clothing and no shoes. | Baseline, week 4, week 8, week 10 |
| Liver function markers (AST, ALT, γ-GT) | Serum liver enzymes assessed for safety. | Baseline and week 8 |
| Kidney function markers (BUN, creatinine, uric acid) | Serum renal parameters assessed for safety. | Baseline and week 8 |
| Change in dietary intake (kcal/day) | Dietary intake will be assessed using 3-day food records analyzed with nutrition analysis software to calculate average daily energy intake (kcal/day). | Baseline, week 4, week 8, week 10 |
| Change in body mass index (BMI, kg/m²) | BMI will be calculated as weight in kilograms divided by height in meters squared. | Baseline, week 4, week 8, week 10 |
| Change in waist circumference (cm) | Waist circumference will be measured at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest, using a standard tape measure. | Baseline, week 4, week 8, week 10 |
| Change in blood pressure (mmHg) | Systolic and diastolic blood pressure will be measured using an automated sphygmomanometer after 5 minutes seated rest. | Baseline, week 4, week 8, week 10 |
| Change in physical activity level (IPAQ-SF score, MET-min/week) | Physical activity will be assessed using the International Physical Activity Questionnaire - Short Form (IPAQ-SF). Scores will be calculated as MET-minutes per week. Higher scores indicate greater physical activity levels. | Baseline, week 4, week 8, week 10 |