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Chia Seeds Consumption in Hypertriglyceridemia

Effects of Chia Seed Consumption in Comparison With Marine Omega-3 Supplementation on the Concentration of Blood Lipid and Inflammatory Factors in Hypertriglyceridemic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06020950
Enrollment
66
Registered
2023-09-01
Start date
2023-09-18
Completion date
2024-03-16
Last updated
2024-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertriglyceridemia

Brief summary

Lifestyle changes including diet therapy and weight loss can improve hypertriglyceridemia (HTG) . Furthermore, increasing omega-3 fatty acids intake has therapeutic effects on HTG. Alpha-linolenic acid is the precursor of long-chain omega-3 fatty acid and it is abundant in sources such as chia seeds and flax seeds. Considering the high fiber and omega-3 content of chia seeds and the existing mechanisms for improving lipid profile through fiber and omega-3, animal studies have shown the positive role of chia seed consumption on lipid profile, glycemic and lipid factors, and inflammation. However, in human studies, conflicting results have been obtained and some studies have shown beneficial effects on blood lipid, glycemic, and inflammatory factors, but in some studies, no effect has been observed. The objective of this study is to determine the effects of chia seed consumption on lipids, glycemic and inflammatory factors in people with HTG.

Detailed description

This study is an unblinded randomized controlled clinical trial. The study will be conducted on people with mild to moderate hypertriglyceridemia whose fasting blood triglyceride levels were between 150-499 mg/dL in the previous two tests. Participants who meet the following criteria will not be included in the study: Being treated with fibrate medications, end-stage kidney disease, acquired immunodeficiency syndrome patients, cancer patients undergoing chemotherapy or radiotherapy, patients with liver cirrhosis, being treated glucocorticoids, continuous use of omega-3 supplements or in the past month, and pregnancy or lactation. Patients will be randomly assigned to one of three study groups. The duration of the study will be 8 week. The groups are: the control group, which is given a placebo pearls containing sunflower oil. the omega-3 oil group will be given omega-3 pearls, and the chia seed group that will consume chia seeds. In addition, the participants of all three groups are subjected to a low-calorie diet. At the beginning and end of the study, the measurements include body weight, blood pressure, blood concentration of lipids, lipoproteins and inflammatory factors.

Interventions

OTHERControl

Low-calorie diet with the use of placebo pearls (containing sunflower oil)

DIETARY_SUPPLEMENTOmega-3 supplementation

Low-calorie diet with the use of marine omega-3 pearls (containing 1200 mg eicosapentaenoic acid + 600 mg docosahexaenoic acid/day)

OTHERChia seed

Low-calorie diet with the consumption of 30 grams of powdered chia seeds

Sponsors

National Nutrition and Food Technology Institute
CollaboratorOTHER
Shahid Beheshti University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* \- Individuals who had fasting triglyceride concentration 150-499 mg/dL in their two previous tests

Exclusion criteria

* Being treated with fibrate medications * Being treated glucocorticoids * Being treated with anticoagulants (except aspirin) * Continuous use of omega-3 supplements or in the past month * End-stage kidney disease * Acquired immunodeficiency syndrome patients * Cancer patients undergoing chemotherapy or radiotherapy * Patients with liver cirrhosis * Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frameDescription
Plasma concentration of triglycerides8 weekFasting plasma concentration of C-reactive protein and IL-6

Secondary

MeasureTime frameDescription
Weight loss8 weekBody wight loss (kg)
Plasma concentration of insulin8 weeksFasting plasma concentration of insulin
Plasma inflammatory factors concentration8 weekFasting plasma concentration of C-reactive protein and IL-6

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026