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CTRI Number  CTRI/2025/08/092191 [Registered on: 01/08/2025] Trial Registered Prospectively
Last Modified On: 31/07/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Physiotherapy (Not Including YOGA) 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   comparison of immediate effect of one using steady pressure on muscle and other using pain free position on pain , range of motion among the college going student with TRAPEZITIS: EXPERIMENTAL STUDY  
Scientific Title of Study   Immediate effect of ischemic compression versus positional release technique on pain, range of motion, among the college going with TRAPEZITIS: EXPERIMENTAL STUDY  
Trial Acronym  nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Jyoti shukla  
Designation  Bpth student  
Affiliation  Dr ulhas patil college of physiotherapy  
Address  Physiotherapy OPD NO 207,NH 06, Gat No. 57 1, Khirdi Shivar, Tal And Dist Jalgaon Jalgaon MAHARASHTRA 425001 India

Jalgaon
MAHARASHTRA
425001
India 
Phone  08451077617  
Fax    
Email  js9682657@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Chaitali neve  
Designation  Assistant professor  
Affiliation  Dr ulhas patil college of physiotherapy 
Address  NH 06, Gat No. 57 1, Khirdi Shivar, Tal And Dist Jalgaon Jalgaon MAHARASHTRA 425001 India

Jalgaon
MAHARASHTRA
425001
India 
Phone  09518719182  
Fax    
Email  chaitalisneve123@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Chaitali neve 
Designation  Assistant professor  
Affiliation  Dr ulhas patil college of physiotherapy  
Address  NH 06, Gat No. 57 1, Khirdi Shivar, Tal And Dist Jalgaon Jalgaon MAHARASHTRA 425001 India

Jalgaon
MAHARASHTRA
425001
India 
Phone  09518719182  
Fax    
Email  chaitalisneve123@gmail.com  
 
Source of Monetary or Material Support  
Dr.Ulhas patil college of physiotherapy, Jalgaon NH 06, Gate no. 57 1, Khirdi Shivari, Tal And Dist Jalgaon,pincode 425003 
 
Primary Sponsor  
Name  Jyoti Shukla  
Address  Dr.Ulhas patil college of physiotherapy, Jalgaon, NH 06, Gat no.57 1,Khirdi Shivar,Tal and Dist Jalgaon, pincode 425309 
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 
Dr chaitali neve   Dr ulhas patil college of physiotherapy  OPD no 207,Physiotherapy OPD, Jalgaon
Jalgaon
MAHARASHTRA 
9518719182

chaitalisneve123@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee of Dr ulhas patil college of physiotherapy  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  trapezitis  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  ischemic compression   Hot pack applied for 15 mins, followed by sustained thumb pressure on latent trigger points of the trapezius for 30 sec–1 min or until tenderness reduces, max up to 90 sec.  
Comparator Agent  Positional release technique   Hot pack applied for 15 mins, then trigger points located. The head is side-flexed, and shoulder abducted to 90°, with fine-tuned position held for 90 sec to release tension. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  26.00 Year(s)
Gender  Both 
Details  Age (18 to 26)
Both male and female
Pain from at least last 15 days
Palpable trigger points in the upper trapezius muscle
Having a pain score 3 to 7 on the visual analogue scale
Limitation of neck movement due to pain
Willingness to participate
 
 
ExclusionCriteria 
Details  Cervical injury
History of referred pain due to cervical pathology
Degenerative cervical spine
Wound over neck region
Shoulder pathology
 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Not Applicable 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
visual analog scale
Cervical range of motion  
preintervention and postintervention immediately after 30 mins of intervention
 
 
Secondary Outcome  
Outcome  TimePoints 
Cervical range of motion   preintervention postintervention immediately after 30 mins of intervention  
 
Target Sample Size   Total Sample Size="40"
Sample Size from India="40" 
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 
Date of First Enrollment (India)   18/08/2025 
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="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    AIM
to compare the immediate effect of ischemic compression versus positional release technique on pain and range of motion among college going student with trapezitis 
OBJECTIVE 
to assess immediate effect of ischemic compression on pain , range of motion among college going student with trapezitis 
to assess effect of positional release technique on pain range of motion among college going student with trapezitis 
to compare the effect between ischemic compression and positional release techniques on pain range of motion among college going student with trapezitis 
PROCEDURE 
permission will be taken from institutional ethical committee 
participants will be selected according to inclusion and exclusion criteria 
consent form will be signed by the participants 
40 subject will be divided in to two groups A and B 
group A will receive ischemic compression and group B will receive positional release technique 
after responses data will be analyzed  
 
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