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Effect of Dietary Fiber on Metabolism, Inflammation and Nutritional Status in Patients With Chronic Diseases

Dietary Fiber in Nutritional Therapy for Chronic Diseases

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04690075
Enrollment
120
Registered
2020-12-30
Start date
2020-12-24
Completion date
2021-06-30
Last updated
2021-01-08

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

Conditions

Chronic Disease, Dietary Fiber

Keywords

dietary fiber, chronic disease, metabolism, inflammation, nutritional status

Brief summary

The prevalence of chronic disease is increasing rapidly in China. Medical nutritional therapy (MNT) is essential for the prevention and control of chronic diseases. For example, dietary fiber plays an important role in chronic disease management. Evidence suggests that increasing fiber intake can decrease the risk of chronic diseases, such as overweight/obesity, hyperlipidemia, hyperglycemia, GI diseases, etc. However, according to the nation-wide survey, the dietary fiber intake of Chinese people shows a downward trend in recent years, and the relationship between dietary fiber and metabolism of chronic patients is still controversial. So, this study aims to explore the effects of dietary fiber on metabolism, inflammatory factors and nutritional status among patients with chronic diseases, so as to provide reference for proper nutrition intervention towards chronic disease.

Detailed description

Investigators plan to recruit potential participants in hospital clinics using posters. An anticipated total of 120 patients with chronic diseases (including overweight, obesity, hyperlipemia, hyperglycemia, etc) will be randomized to receive oat beta-glucans (study group) or routine nutrition management (control group) respectively. The outcome parameters, including weight, blood glucose level, blood fat level, etc, will be measured and compared over a 12-week intervention period. Intention-to-treat analysis (ITT) and per-protocol analysis (PP) will be conducted in statistical analysis.

Interventions

DIETARY_SUPPLEMENTNutrition Management and Dietary Fiber

Routine nutrition management and dietary fiber supplements based on recommendation for 12 weeks.

DIETARY_SUPPLEMENTNutrition Management

Routine nutrition management for 12 weeks.

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Age 18-70y * Be diagnosed with obesity, hyperlipemia or hyperglycemia * Fully understood and voluntarily signed the informed consent

Exclusion criteria

* Secondary hyperlipidemia or hyperglycemia * Multiple organ failure * Allergic or intolerant to dietary fiber(dietary supplement) * Have gastrointestinal diseases * Have a history of abdominal diseases * Experienced intra-abdominal surgery * Pregnant and lactating women

Design outcomes

Primary

MeasureTime frameDescription
Change of total cholesterol (TC) levelbaseline, 12 weeksTotal cholesterol (TC) level obtained from laboratory test
Change of low density lipoprotein (LDL) cholesterol levelbaseline, 12 weeksLow density lipoprotein (LDL) cholesterol level obtained from laboratory test

Secondary

MeasureTime frameDescription
Change of triglyceride (TG) levelbaseline, 12 weeksChange of triglyceride (TG) level obtained from laboratory test
Change of high density lipoprotein (HDL) cholesterol levelbaseline, 12 weeksChange of high density lipoprotein (HDL) cholesterol level obtained from laboratory test
Change of fasting blood glucose (FBG) levelbaseline, 12 weeksChange of fasting blood glucose (FBG) level obtained from laboratory test
Change of 2 hours postprandial blood glucose levelbaseline, 12 weeksChange of 2 hours postprandial blood glucose level obtained from laboratory test
Change of interleukin-6 (IL-6) levelbaseline, 12 weeksInterleukin-6 (IL-6) level obtained from laboratory test
Change of total body fat levelbaseline, 12 weeksChange of total body fat level obtained from bioelectrical impedance analysis
Change of Percent of body fat (PBF) levelbaseline, 12 weeksChange of percent of body fat (PBF) level obtained from bioelectrical impedance analysis
Change of visceral fat area (VFA) levelbaseline, 12 weeksChange of visceral fat area (VFA) level obtained from bioelectrical impedance analysis
Change of hemoglobin levelbaseline, 12 weeksChange of hemoglobin level obtained from laboratory test
Change of tumor necrosis factor-alpha levelbaseline, 12 weeksChange of tumor necrosis factor-alpha level obtained from laboratory test

Countries

China

Contacts

Primary ContactKang Yu, M.D.
yuk1997@sina.com+86 01-69155550
Backup ContactXiaodong Nie, Dr
drdoranie@gmail.com+8615832108663

Outcome results

None listed

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