None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Overweight individuals (Body Mass Index between 25-30) with controlled co-morbid dyslipidemia and/or hypertension and/or type 1 or type 2 diabetes 2.Stable body weight (less than 5 kg self-reported change during the previous 3 months) 3.Age between 18 years and 60 years 4.Individuals found compliant based on the Million Behavioural Medicine Diagnostic (MBMD) 5.Willing to give Informed consent before any trial-related activity takes place
Exclusion criteria
Exclusion criteria: 1.Known case of endocrinological disorders such as hyper/hypo thyroidism, Poly Cystic Ovarian Syndrome (PCOS) 2.History of use one month before screening /currently using Allopathic or Ayurvedic medicines that may cause significant weight gain 3.History of use one month before screening /currently using dietary supplements, over-the-counter medications or below mentioned Allopathic /Ayurvedic medicines for weight loss 4.Current participation (past one month) in an organized weight reduction program â?? 5.Participants with a history of major depressive or other severe psychiatric disorders or an eating disorder [judged by frequency and quantity of food] 6.Surgery scheduled for the trial duration period, except for minor surgical procedures, at the discretion of the investigator 7.Pregnant or lactating females
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The outcome of the study will be measured in terms of anthropometric measurements (Weight, Body Mass Index, Waist Hip Ratio, Circumferences, Skinfold thicknesses)and Clinical signs and symptoms.Timepoint: After every 15 days | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome of the study will be measured on the basis of biochemical profiling of obesity markers.Timepoint: Day 0,Day 30,Day 60,Day 90, Day 120 | — |
Countries
India
Contacts
Interactive Research School for Health Affairs