Overweight/obesity, Bone mass loss
Conditions
Interventions
Experimental group:Flavanols
Control group:Plus placebo (wheat flour )
Sponsors
Southern Medical University
Eligibility
Sex/Gender
All
Age
40 Years to 60 Years
Inclusion criteria
Inclusion criteria: Overweight/obese patients aged 40-60 years with BMI>=24.0kg/m^2.
Exclusion criteria
Exclusion criteria: Patients with chronic diseases such as diabetes, cirrhosis, kidney disease, cancer, and severe gastrointestinal diseases; Mental abnormality or low intelligence, disability or life can not take care of themselves; A history of fracture; Pregnant women, women planning to become pregnant within 2 months and lactating women; Use of probiotics or prebiotics in the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone mineral density/bone mineral content at the left hip, lumbar spine, and whole body;Content of body fat; | — |
Secondary
| Measure | Time frame |
|---|---|
| Liver ultrasonography indicators; | — |
Countries
China
Contacts
Public ContactZheqing Zhang
Southern Medical University
Outcome results
None listed