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CTRI Number  CTRI/2025/07/090408 [Registered on: 07/07/2025] Trial Registered Prospectively
Last Modified On: 09/12/2025
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   Cross Sectional Study 
Study Design  Other 
Public Title of Study   assessment of proportion of Cardiovascular disease risk among young IT professionals working in Metro city of Western Region of Maharashtra.  
Scientific Title of Study   Prevalence of Cardiovascular disease risk among young adults in IT profession working in Metro city of Western Region of Maharashtra. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Aditi L Soman 
Designation  Assistant Professor 
Affiliation  Deccan Education Society’s, Brijlal Jindal College of Physiotherapy, Pune 
Address  D.E.Societys Brijlal Jindal college of physiotherapy

Pune
MAHARASHTRA
411004
India 
Phone  918788123192  
Fax    
Email  aditi.soman@despune.org  
 
Details of Contact Person
Scientific Query
 
Name  Dr. Ruthvija Jadhav 
Designation  PG student 
Affiliation  Deccan Education Society’s, Brijlal Jindal College of Physiotherapy, Pune 
Address  D.E.Societys Brijlal Jindal college of physiotherapy

Pune
MAHARASHTRA
411004
India 
Phone  918788123192  
Fax    
Email  jadhavruthvija@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Aditi L Soman 
Designation  Assistant Professor 
Affiliation  Deccan Education Society’s, Brijlal Jindal College of Physiotherapy, Pune 
Address  D.E.Societys Brijlal Jindal college of physiotherapy


MAHARASHTRA
411004
India 
Phone  918788123192  
Fax    
Email  aditi.soman@despune.org  
 
Source of Monetary or Material Support  
Nil 
 
Primary Sponsor  
Name  Dr. Aditi Soman 
Address  D.E.Societys Brijlal Jindal college of physiotherapy 
Type of Sponsor  Other [self funded] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Ruthvija Jadhav  DESBJCOP OPD, community setting  Fergusson College Campus, F. C .main gate, Shivajinagar
Pune
MAHARASHTRA 
918788123192

jadhavruthvija@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
DECCAN EDUCATION SOCIETYS BRIJLAL JINDAL COLLEGE OF PHYSIOTHERAPY ETHICS COMMITTEE   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  IT Professionals 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Nil  Nil 
Intervention  Nil  Nil 
Intervention  Nil  Nil 
Intervention  Nil  Nil 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  30.00 Year(s)
Gender  Both 
Details  Inclusion Criteria :-
1. working hours more than 6hours per day
2. Age 18 -30 Years
3.Male and female gender
4.Individuals having at least 5 years of experience.
5.Individuals who are willing to participate.


 
 
ExclusionCriteria 
Details  Exclusion Criteria
1.Pregnancy
2.Individuals whoever are on medication of sleep or stress
3.Acute illness and physical disability
4.Individuals having any cardiovascular disease, diabetes
5.Incomplete data
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Interheart modifiable risk questionnaire   1, taken only once/single assessment 
 
Secondary Outcome  
Outcome  TimePoints 
none  none 
 
Target Sample Size   Total Sample Size="112"
Sample Size from India="112" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   30/07/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Background: Concerns regarding the risk of cardiovascular disease (CVD), especially in young adults, have been raised by the increasing prevalence of sedentary lifestyles among information technology (IT) professionals. High levels of stress, long workdays, and lack of physical activity are all major contributors to modifiable risk factors for CVD.

Need of the Study: Cardiovascular disease remains the leading global cause of morbidity and mortality, with modifiable risk factors playing a central role in its progression. Early identification and intervention are especially crucial in high-risk occupational groups such as IT professionals. Young adults (18–30 years) in this field often face demanding schedules that contribute to physical inactivity, poor dietary habits, stress, and inadequate sleep—conditions that significantly elevate CVD risk. By focusing on this demographic, the study aims to detect early cardiovascular risk and support timely preventive measures.

Objective: This study aims to assess the prevalence of cardiovascular disease risk among young adults (aged 18–30) working in the IT sector in a metropolitan city in the western region of Maharashtra, using the INTERHEART Modifiable Risk Score.

Methodology: A convenience sampling technique will be used to pick 112 participants for a cross-sectional study. IT workers with at least 5 years of experience and more than 6 hours of work each day are eligible to participate. Demographic profile and the INTERHEART risk questionnaire will be used in the data collection process. To determine the prevalence of CVD risk, statistical analysis will be performed using paired t-tests.

 

 
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