Health Condition 1: E663- Overweight
Conditions
Interventions
None listed
Sponsors
National institute of Ayurveda Deemed to be university
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age: Participants aged between 20 and 60 years. 2. Overweight Status: Individuals with a BMI (Body Mass Index) ranging from 25 to 30 kg/m², indicating overweight status. 3. Health Status: Participants without any significant medical conditions, such as cardiovascular diseases, diabetes, or metabolic disorders, that may interfere with the study outcomes. 4. Weight Stability: Individuals with stable body weight (±2 kg) for at least three months before the study initiation. 5. Willingness to Comply: Participants willing to adhere to the prescribed millet-based dietary intervention for the entire study duration. 6. Ability to Give Consent: Individuals capable of providing informed consent for participation in the study.
Exclusion criteria
Exclusion criteria: 1. Age and Gender: Participants having age less than 20 years or more than 60 years are Excluded. 2. BMI Status: Individuals with a BMI below 25 kg/m² (not overweight) or above 30 kg/m² (obese). 3. Medical Conditions: Participants with a history of significant medical conditions, such as heart disease, diabetes, renal disorders, or thyroid dysfunction. 4. Allergies or Intolerances: Participants with known allergies or intolerances to millets or any components of the millet-based dietary intervention. 5. Pregnancy and Lactation: Pregnant or lactating individuals, as the dietary intervention may not be suitable during these periods. 6. Participation in Other Studies: Participants currently enrolled in other clinical studies or interventions related to weight management or nutrition. 7. Medication Use: Individuals taking medications or supplements known to affect weight or metabolic parameters. 8. Uncontrolled Hypertension: Participants with uncontrolled hypertension (systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg). 9. Mental Health Concerns: Individuals with significant mental health conditions or eating disorders that could affect dietary adherence.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study is the change in body weight and BMI. after the millet-based dietary intervention. This outcome will assess the effectiveness of the millet diet in promoting weight reduction in participants with MedoVriddhi (overweight). Body weight will be measured at baseline (before the intervention) and at the end of the intervention period.Timepoint: at baseline to 2 nd week of Intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Body Composition 2. Metabolic Parameters 3. Adherence to the Millet Diet 4. Safety & Adverse Events 5. Changes in Quality of Life:Timepoint: at baseline to 4-6 weeks | — |
Countries
India
Contacts
Public ContactDr. viramgama jinal khodidasbhai
National institute of Ayurveda deemed to be university ,jaipur
Outcome results
None listed