None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants who are overweight and obese Age group 30 to 65 yrs, both males and females Willing to follow study protocol Willing to give informed consent
Exclusion criteria
Exclusion criteria: BMI less than 22.9 kg/m2 On insulin injections Any acute infections like viral fever, typhoid, cold, diarrhea, constipation last 1 month Having diabetes, diabetes induced/related complications [nephropathy, retinopathy]- thyroid dysfunction, respiratory disorders, cancer or heart attack and stroke, Having any eating disorder or lactose intolerance Taking any herbal/Ayurvedic/traditional preparation/nutrition supplements that could profoundly affect blood glucose Pregnant and lactating Women Plans to relocate in the next 2 years. Planning longer duration of travel out of town Enrolled in any other clinical trials Participated in a clinical study in the last 3 months Employee of the site conducting the study. Participants with habitual abuse (Alcohol, smoking, tobacco) substance consumption
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effect of peanut administered for 16 weeks on markers of glycemic- HbA1c, fasting and post glucose, dyslipidemia-total cholesterol, HDL,LDL and triglyceride levels, body composition-weight, body mass index and waist circumference and inflammatory markers as compared to control group.Timepoint: Blood samples will be collected at 2 time points baseline and end of 16 weeks study period. Inaddition participant will be contacted by the research team monthly once for anthropometric, clinical and dietary assessments. | — |
Secondary
| Measure | Time frame |
|---|---|
| Examine peanut supplementation will have beneficial effects on measures of cognition, sleep quality & mood as compared to control group.Timepoint: 2 time points baseline & end of 16 weeks study period. | — |
Countries
India
Contacts
Madras Diabetes Research Foundation