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CTRI Number  CTRI/2026/02/104194 [Registered on: 18/02/2026] Trial Registered Prospectively
Last Modified On: 10/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Physiotherapy (Not Including YOGA) 
Study Design  Non-randomized, Active Controlled Trial 
Public Title of Study   To find out whether a special shoulder movement technique along with regular physiotherapy helps reduce pain, improve daily activities, hand strength, and quality of life in people with frozen shoulder. 
Scientific Title of Study   Effect of gongs mobilisation with conventional therapy on pain functional disability hand grip strength and quality of life in adhesive capsulitis patients 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Afra Siddiqui  
Designation  Student  
Affiliation  Sharda University  
Address  Plot No. 32-34, Knowledge Park III, Greater Noida, Uttar Pradesh - 201306, India

Gautam Buddha Nagar
UTTAR PRADESH
201306
India 
Phone  7408973467  
Fax    
Email  2024273528.afra@pg.sharda.ac.in  
 
Details of Contact Person
Scientific Query
 
Name  Afra Siddiqui  
Designation  Student  
Affiliation  Sharda University  
Address  Plot No. 32-34, Knowledge Park III, Greater Noida, Uttar Pradesh - 201306, India

Gautam Buddha Nagar
UTTAR PRADESH
201306
India 
Phone  7408973467  
Fax    
Email  2024273528.afra@pg.sharda.ac.in  
 
Details of Contact Person
Public Query
 
Name  Afra Siddiqui  
Designation  Student  
Affiliation  Sharda University  
Address  Plot No. 32-34, Knowledge Park III, Greater Noida, Uttar Pradesh - 201306, India

Gautam Buddha Nagar
UTTAR PRADESH
201306
India 
Phone  7408973467  
Fax    
Email  2024273528.afra@pg.sharda.ac.in  
 
Source of Monetary or Material Support  
Department of Physiotherapy, Sharda Hospital 
 
Primary Sponsor  
Name  Afra Siddiqui  
Address  Plot No. 32-34, Knowledge Park III Greater Noida Uttar Pradesh 201306 India 
Type of Sponsor  Other [Physiotherapy ] 
 
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 Rita Sharma PT  Sharda Hospital.  Plot 32 34 knowledge park 3 Greater Noida Uttar Pradesh 201310 India
Gautam Buddha Nagar
UTTAR PRADESH 
81781 54869

rita.sharma@sharda.ac.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Adhesive Capsulitis 
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Group A Gongs Mobilisation  Patient in supine position therapist applied sustained glide to the shoulder 5 sessions per week for 4 weeks 
Comparator Agent  Group B Conventional therapy  Strengthening exercise stretching exercise ultrasound, rope pulley exercise 5 sessions per week for 4 weeks  
Comparator Agent  Group C  Gongs Mobilisation with Conventional therapy 5 sessions per week for 4 weeks  
 
Inclusion Criteria  
Age From  41.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Subjects with frozen shoulder diagnosed by orthopaedician
Subjects with stage II and stage III of adhesive capsulitis
Subjects of both genders between the age group of 41–60 years
Subjects with restricted ROM
 
 
ExclusionCriteria 
Details  Subjects with rotator cuff tears
Overuse injury
History of RA, OA, and malignancies in the shoulder region
Frozen shoulder secondary to neurological disorder
Post-surgical cases 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Independent Vriables
Pain Level will be measured by NPRS (Numeric Pain Rating Scale)
Functional Disability and Quality of Life will be measured by Shoulder Pain and Disability Index (SPADI)
Quality of Life will be measured by SF-36
Hand grip strength will be measured by Jamar Hand Grip Dynamometer 
4 Weeks 
 
Secondary Outcome  
Outcome  TimePoints 
Pain Level will be measured by NPRS Numeric Pain Rating Scale
Functional Disability Quality of Life will be measured by Shoulder Pain Disability Index SPADI
Quality of Life will be measured by SF-36
Hand grip strength will be measured by Jamar Hand Grip Dynamometer 
4 Weeks 
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
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)   03/03/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  03/03/2026 
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)   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  
Patient will receive informed consent before beginning of the study.Patients will be provided with detailed explanation about safety procedures and purpose of the study including sign symptoms and possible outcomes 
Patient will be randomly divided into three groups 

Group A- (Gong’s mobilisation) patient position in supine position focusing on shoulder joint mobilisation on capsular stretching treatment was given 5 session per week for 4 weeks with 10 - 15 repetition per session
Group B - (conventional therapy) recieved codman pendulum exercise ,finger ladder exercise towel strengthening rope and pulley exercises anterior shoulder stretching therapeutic ultrasound for 5 session per week for 4 weeks
Group C- Gong’s Mobilisation with conventional therapy administered 5 sessions per week for 4 weeks
 
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