A study to assess the effectiveness of self managementprogram on Metabolic Syndrome risk reduction among middle and old-aged adults ofthe selected villages of Rajpura, Punjab.

Not yet recruiting

• Conditions: volunteers who will be found have metabolic syndrome after screening as per modified NCEP ATP III criteria.

• Registration Number: CTRI/2023/04/051334
• Lead Sponsor: Chitkara University, Punjab

Brief Summary

this study has  been  undertaken to for metabolic syndrome risk reduction in adults of selected villages. Geographically stratified sampling procedure was used to select  villages,  two for intervention group and 2 for control group to prevent contamination.

After receiving CTRI number, participants  will recruited to both the groups with the help of ASHA workers of selected villages via door to door survey and as per inclusive and exclusive criteria  Intervention that is self management program will be delived to intervention group and standard care to control group.



Total duration of  intervention will be 6 months and at 6 months data will collected from both the groups to compare with baseline data.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-03-04
• Study Start: 2023-04-15

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 154

Inclusion Criteria

• Participants who are willing to enroll in the study 2.
• Adults who will be found to have metabolic syndrome after screening 3.
• Participants who have access to mobile phone.

Exclusion Criteria

• Already diagnosed with diabetes mellitus (other than gestational diabetes), heart diseases and stroke, cancer.
• Presently on weight loss diet.
• Enrolled in any other physical activity program.
• Enrolled in any other nutritional program.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
reduction in number of risk factors of metabolic syndrome either physiological risk factors (Waist circumference, Blood pressure) and biochemical risk factors (FBS, TG, HDL level) in intervention group than baseline.	time points: baseline, 4 weeks, 3 months, 6 months

Secondary Outcome Measures

Name	Time	Method
decrease in behavioural risk factors (physical activity, adequate diet intake, tobacco & alcohol intake) in intervention group.	total duration of intervention is 6 months.

Trial Locations

Locations (1)

Villages Thua, Sham duon, Kehri Gurna, Sham duon camp of Tehsil Rajpura, Punjab; 🇮🇳 Patiala, PUNJAB, India

Villages Thua, Sham duon, Kehri Gurna, Sham duon camp of Tehsil Rajpura, Punjab

🇮🇳Patiala, PUNJAB, India

Gaurav Kholi

Principal investigator

9778898245

gaurav.kohli@chitkara.edu.in