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Yoga Module and atis (herb)in overweight: An RCT

Evaluating the Efficacy of Yoga Module and Aconitum heterophyllum Wall.Ex Royle (Atis) for the Management of Sthaulya (Overweight) with Comorbid Psychological Conditions: A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093910
Enrollment
120
Registered
2025-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: E669- Obesity, unspecified

Interventions

Intervention1: Group A ? Yoga Module for Obesity
Group B ? Aconitum heterophyllum Wall. Ex Royle (processed root powder): Group A will practice a structured yoga program for 60 minutes, 6 days/week for 90 days. Group B will take a standardized dose
Group B ? Aconitum heterophyllum Wall. Ex Royle (processed root powder)
Group C ? Control: Group A will practice a structured yoga program for 60 minutes, 6 days/week for 90 days. Group B will take a standardized dose of processed Aconitum heterophyllum root powder orally

Sponsors

Km Mamta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age-18 to 50 years With BMI greater than 24.5 Non yoga practioners Commitment to follow up intervention General diet recommendation

Exclusion criteria

Exclusion criteria: Regular yoga practitioners Alcohol or substance abuse Pregnancy or lactation Severe psychiatric disorders

Design outcomes

Primary

MeasureTime frame
Change in Body Weight, BMI, Waist Circumference, and Waist-Hip Ratio from baseline week 0 to 12.Timepoint: Baseline (week 0): Before starting the intervention End of Study(week 12): After completion of the intervention.

Secondary

MeasureTime frame
Psychological & quality of life parameters: Changes in Depression, Anxiety, & Stress measured by DASS-21, eating behavior patterns measured by EAT-26, & obesity-related quality of life measured by WHOQOL.Timepoint: Baseline (Week 0): Before starting the intervention End of Study (Week 12): After completion of the intervention.

Countries

India

Contacts

Public ContactDrRajesh Mishra

evam Anusandhan Sansthan

rajesh.mishra@prft.co.in7895979176

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026