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YOGA based diabetes prevention trial

Yoga programme for type-2 diabetes prevention (YOGA-DP) among high-risk people in India: intervention development and feasibility study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/018893
Enrollment
64
Registered
2019-05-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: From first to fourth week at least two sessions per week (45 mins/session). The instructor will maintain an attendance register. From fifth to 12th week At least two sessions per week (

Sponsors

UK DfID UK MRC and the NIHR AND Wellcome Trust Joint Global Health Trials
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Aged 18-74 years. At high-risk of T2DM (fasting plasma glucose level from 100 to 125 mg/dL). Safe to participate in physical activities (assessed using the Physical Activity Readiness Questionnaire). Willing and able to attend the intervention/control sessions on their own. Able to provide written informed consent.

Exclusion criteria

Exclusion criteria: Pregnant women. Those with any serious or uncontrolled medical condition (e.g., cancer). Those who regularly practice yoga i.e., >= 150 minutes/week. Those currently receiving (or has plans to receive during the study period) any related non-pharmaceutical/pharmaceutical intervention

Design outcomes

Primary

MeasureTime frame
Standard deviation (SD) of the outcome measure (i.e., difference in mean change (from the baseline to 6-month) in fasting plasma glucose level between the two treatment arms), which will be used to calculate sample size of the future RCT; reported.Timepoint: Baseline and 6 months

Secondary

MeasureTime frame
Number of people screened for eligibility, Number of participants followed-up at 6-month; Number of yoga sessions attended out of the total number of session; Time needed to collect and analyse data and socio-demographic information, medical history, medications, family history of diabetes, biochemical parameters, physiological parameters, anthropometric parameters, lifestyle factors, EQ-5D, depression, DASS-21, yoga practice, and self-efficacy assessment.Timepoint: Baseline and 6 months

Countries

India

Contacts

Public ContactPallavi Mishra

Centre for Chronic Disease Control

kavita@ccdcindia.org011-41618456

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 17, 2026