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CTRI Number  CTRI/2026/02/103504 [Registered on: 10/02/2026] Trial Registered Prospectively
Last Modified On: 09/02/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Yoga & Naturopathy 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Effect of Yoga on Work Related Muscle and Joint Problems in IT Professionals 
Scientific Title of Study   Effect of Yogic Practices on Biochemical Markers of Work-related Selected Musculoskeletal Disorders among IT Professionals  
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Pedasingu Sharmila Devi 
Designation  Ph.D. Scholar 
Affiliation  Central University of Kerala 
Address  Department of the Yoga Studies, Yamuna Block, Central University of Kerala, Tejaswini Hills, Periye (PO), Kasaragod, Kerala - 671325

Kasaragod
KERALA
671325
India 
Phone  7310573130  
Fax    
Email  pedasingusharmiladevi.2302207007@cukerala.ac.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr.M.Anjaladevi 
Designation  Assistant Professor 
Affiliation  Central University of Kerala 
Address  Department of the Yoga Studies, Yamuna Block, Central University of Kerala, Tejaswini Hills, Periye (PO), Kasaragod, Kerala - 671325

Kasaragod
KERALA
671325
India 
Phone  9789253529  
Fax    
Email  anjaladevi.m@cukerala.ac.in  
 
Details of Contact Person
Public Query
 
Name  Pedasingu Sharmila Devi 
Designation  Ph.D. Scholar 
Affiliation  Central University of Kerala 
Address  Department of the Yoga Studies, Yamuna Block, Central University of Kerala, Tejaswini Hills, Periye (PO), Kasaragod, Kerala - 671325

Kasaragod
KERALA
671325
India 
Phone  7310573130  
Fax    
Email  pedasingusharmiladevi.2302207007@cukerala.ac.in  
 
Source of Monetary or Material Support  
Cybercity Marina Skies, Green Hills Rd, opp. to IDL Lake Road, Cybercity, Kukatpally, Hyderabad, Telangana 500018 
 
Primary Sponsor  
Name  Central University of Kerala 
Address  Central University of Kerala, Tejaswini Hills, Periye, Kasaragod, Kerala -671325 
Type of Sponsor  Research institution 
 
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 
Pedasingu Sharmila Devi  Cybercity Marina Skies Residential Community  Cybercity Marina Skies Residential Community, Yoga Hall, Club house Green Hills Road, Opposite IDL Lake Road Cybercity, Kukatpally, Hyderabad, Telangana - 500018, India
Hyderabad
TELANGANA 
7310573130

pedasingusharmiladevi.2302207007@cukerala.ac.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Human Ethics Committee (IHEC), Central University of Kerala  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:G560||Carpal tunnel syndrome. Ayurveda Condition: NANATMAJAVATAVIKARAH, (2) ICD-10 Condition:M545||Low back pain. Ayurveda Condition: NANATMAJAVATAVIKARAH, (3) ICD-10 Condition:M501||Cervical disc disorder with radiculopathy. Ayurveda Condition: NANATMAJAVATAVIKARAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmProcedure-NA (Procedure Reference: (Garfinkel et al., 1984); (Pravalika et al., 2023); (Kim, 2018), Procedure details: All the participants in yoga groups will follow the Yogic Intervention for 60 minutes, 6 days per week. This Yogic Intervention is prepared from the evidence of previous studies(Garfinkel et al., 1984); (Pravalika et al., 2023); (Kim, 2018))
 
Inclusion Criteria  
Age From  30.00 Year(s)
Age To  45.00 Year(s)
Gender  Both 
Details  Participants must be between 30 and 45 years of age.
Participants must be currently employed as an information technology professional with a minimum of two years of work experience in the industry.
Participants must have a clinically diagnosed work related musculoskeletal disorder such as Carpal Tunnel Syndrome Cervical Radiculopathy or Lower Back Pain confirmed through physical examination and appropriate diagnostic tests including Tinel sign Phalen test Spurling test and straight leg raise test.
Participants must work at least thirty five hours per week in a predominantly sedentary occupation involving prolonged computer use.
Participants must be willing to participate in a twelve week yogic intervention program and comply with the study protocol.
Participants must provide written informed consent prior to participation in the study. 
 
ExclusionCriteria 
Details  Individuals with severe or advanced musculoskeletal disorders requiring surgical intervention or those who have undergone musculoskeletal surgery within the past one year.
Participants with chronic medical conditions such as cardiovascular diseases or autoimmune disorders that may influence the study outcomes.
Individuals who have practiced yoga or similar physical activity programs such as Pilates or Tai Chi on a regular basis more than twice per week during the previous six months.
Pregnant women or women planning pregnancy during the study period.
Participants with severe psychiatric illness or cognitive impairment that may interfere with adherence to the study protocol.
Individuals who are currently participating in any other clinical trial or therapeutic intervention that could affect the study outcomes. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Change in biochemical markers including inflammatory markers IL1 IL6 and TNF alpha oxidative stress markers ROS MDA and SOD and neurotrophic factors NGF BDNF and Neurotrophin three from baseline to post intervention in information technology professionals with work related musculoskeletal disorders such as Carpal Tunnel Syndrome Cervical Radiculopathy and Lower Back Pain following yogic practices compared to a control group.  Baseline
At twelve weeks post-intervention 
 
Secondary Outcome  
Outcome  TimePoints 
Change in Tinel’s Sign, Phalen’s Test, Spurling’s Test, and Straight Leg Raise Test results  baseline (Week 0) and post-intervention (Week 12) 
Change in Electromyography (EMG)  baseline (Week 0) and post-intervention (Week 12) 
hange in functional disability assessed by disease-specific scales (DASH for Carpal Tunnel Syndrome, Neck Disability Index for Cervical Radiculopathy, Oswestry Disability Index for Low Back Pain)  baseline (Week 0) and post-intervention (Week 12) 
 
Target Sample Size   Total Sample Size="134"
Sample Size from India="134" 
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)   01/04/2026 
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="0"
Months="3"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
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   This randomized controlled trial aims to evaluate the effect of a structured yogic practice program on biochemical and clinical outcomes of selected work-related musculoskeletal disorders among information technology professionals. Eligible participants diagnosed with carpal tunnel syndrome, cervical radiculopathy, or lower back pain will be screened and randomly assigned to experimental and control groups. The experimental group will receive a 12 week yogic practice program while the control group will continue routine lifestyle practices without intervention. The primary outcomes include changes in biochemical markers such as inflammatory markers, oxidative stress markers, and neurotrophic factors. Secondary outcomes include improvements in clinical assessment tests, electromyography, reduced pain, improved musculoskeletal function, and enhanced occupational performance. The study aims to establish yoga as a cost effective safe and non invasive intervention for promoting health and productivity among information technology professionals with work related musculoskeletal disorders. 
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