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CTRI Number  CTRI/2026/01/101310 [Registered on: 16/01/2026] Trial Registered Prospectively
Last Modified On: 15/01/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Physiotherapy (Not Including YOGA) 
Study Design  Randomized, Parallel Group, Multiple Arm Trial 
Public Title of Study   Effect of Dry Needling, Myofascial Release, and Positional Release Therapy on Neck Disability (NDI) in College Students with Trapezius Myalgia 
Scientific Title of Study   Short Term Effectiveness Of Dry Needling, Myofascial Release Technique And Positional Release Therapy On Neck Function In College Students With Trapezius Myalgia: A Single Blinded Randomised Clinical Trial 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
Nil  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Vrutika Naik 
Designation  Post graduate of Physiotherapy  
Affiliation  Institute of Physiotherapy, Srinivas University  
Address  Institute Of Physiotherapy, Srinivas University, Department of Musculoskeletal and Sports Physiotherapy, ground floor, city campus, Pandeshwar Mangaluru

Dakshina Kannada
KARNATAKA
575001
India 
Phone  9764912599  
Fax    
Email  vrutikanaik02@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Premkumar M 
Designation  Professor  
Affiliation  Institute of Physiotherapy, Srinivas University  
Address  Institute of Physiotherapy, Srinivas University, Department of cardiopulmonary Physiotherapy, ground floor, city campus, Pandeshwar, Manguluru

Dakshina Kannada
KARNATAKA
575001
India 
Phone  9442508754  
Fax    
Email  80pk2009@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Vrutika Naik 
Designation  Post graduate of Physiotherapy  
Affiliation  Institute of Physiotherapy,Srinivas University  
Address  Institute of Physiotherapy, Srinivas University, Department of Musculoskeletal and Sports Physiotherapy, ground floor, city campus, Pandeshwar Manguluru

Dakshina Kannada
KARNATAKA
575001
India 
Phone  9764912599  
Fax    
Email  vrutikanaik02@gmail.com  
 
Source of Monetary or Material Support  
Nil  
 
Primary Sponsor  
Name  Vrutika Naik 
Address  Institute of Physiotherapy, Srinivas University, Department of Musculoskeletal and Sports Physiotherapy, ground floor, city campus, Pandeshwar Manguluru Karnataka India 575001 
Type of Sponsor  Other [Self] 
 
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 
Vrutika Naik   Institute of Physiotherapy, Srinivas University, MSD , Pandeshwar Manguluru   Institute of Physiotherapy, Srinivas University, Department of Musculoskeletal And Sports Physiotherapy ground floor, city campus, Pandeshwar Manguluru
Dakshina Kannada
KARNATAKA 
9764912599

vrutikanaik02@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Review Board And Ethical Committee (IRBEC)  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Trapezius myalgia  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Dry Needling   Group A will receive DN in a single session. The needle will be placed into the Trp of trapezius muscle using fast in and out technique 10 times. Conventional exercises  
Intervention  MFR  A single 12 minutes session of MFR will be performed using a hands on approach. Conventional exercises. 
Comparator Agent  Not applicable   Not applicable  
Intervention  Positional release therapy   Once the tender point is found the therapist will squeeze the muscle between thumb and finger to provide pressure. Abduct shoulder to about 90 degree and add lateral flexion of the subject head towards the side of painful spot. For 90 second posture should maintain and then relax position. Conventional exercises. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  26.00 Year(s)
Gender  Both 
Details  Pain intensity of 3 and above on VAS and presence of restricted cervical range of motion.
Latent trigger point in the neck region, participants with unilateral and bilateral tender point.
Participants who have agreed to sign a written consent form. 
 
ExclusionCriteria 
Details  Recent trauma to the cervical region, participants on any anti-inflammatory drugs.
Recent cervical pathologies like myelopathy, radiculopathy, herniated disc, spinal stenosis.
Skin disease surrounding the area that need to be addressed.
Brachial neuralgia.
Fear of needles. 
 
Method of Generating Random Sequence   Other 
Method of Concealment   Other 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
Pressure pain threshold   At baseline and after one week  
 
Secondary Outcome  
Outcome  TimePoints 
VAS, CROM, GROC, NDI  At baseline and after one week  
 
Target Sample Size   Total Sample Size="99"
Sample Size from India="99" 
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   Phase 2/ Phase 3 
Date of First Enrollment (India)   02/02/2026 
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="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
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   Neck pain is prevalent musculoskeletal condition. Localised neck pain is becoming more frequent often it’s  affects the upper portion of the trapezius muscle.The protocol includes Dry needling, positional release therapy and Myofascial release technique.
The participants will be recruited who has pain intensity 3 and above on VAS, restricted cervical range, latent trigger point and unilateral and bilateral tender point. Exclusion criteria includes recent trauma to cervical region, recent cervical pathologies and skin diseases. Outcome measures are pressure pain threshold, CROM , VAS, GROC and NDI. It should be noted at pre and postoperative intervention and after a week. Follow up will be done after one week. 
 
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