- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07628335
Effects of Gong's Mobilization With and Without Nielasher Technique on in Adhesive Capsulitis
Effects of Gong's Mobilization With and Without Niel Asher Technique on Shoulder Pain, Range of Motion and Disability in Adhesive Capsulitis
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: iqbal Tariq, phd
- Phone Number: 03338236752
- Email: iqbal.tariq@riphah.edu.pk
Study Contact Backup
- Name: Rabiya Noor, phd
- Phone Number: 03344355660
- Email: Rabiya.Noor@riphah.edu.pk
Study Locations
-
-
Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Recruiting
- Rabiya Noor
-
Contact:
- iqbal Tariq, phd
- Phone Number: 03338236752
- Email: iqbal.tariq@riphah.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals with age group of 40-60 years.
- Both Females and males individuals.
- Individuals diagnosed with Frozen shoulder (Adhesive Capsulitis) within stage II and III of frozen shoulder.
- Individuals with positive capsular pattern (ER>Abd> IR).
- Individuals with ROM loss ≥ 25% in at least two planes compared with the noninvolved shoulder
Exclusion Criteria:
- Individuals with rotator cuff tears and overuse injury
- Individuals with inflammatory diseases (Osteoarthritis, Rheumatoid Arthritis, Gout) and Malignancies
- Individuals Using Corticosteroid Injections or Medications
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Gong's Mobilization
|
It is performed in a side-lying position.
|
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Active Comparator: Gong's Mobilization and Niel-Asher technique
|
It is performed in a side-lying position.
1. In Niel-Asher technique, the patient was made to lie sideways and several deep strokes with your hand, from elbow to humeral head were applied. Apply sustained pressure over the embedded nodules or over the fibrous band which you may feel when you move upwards. 2. Apply deep sustained pressure on the tender point over the posterior joint capsule area (teres minor). 3. Perform circumduction of shoulder with bent elbow repeatedly several times from small to large complete circles. 4. Release the fascia up the long head biceps tendon and move upwards only. Pause on the nodules along the tendon; these are fascial tethering and may be inflamed. As you approach the shoulder, near the biceps tendon joins the capsule, hold the trigger point for up to three minutes until it is completely pain free. 5.In supine lying position, the middle fingers of your hand, presses deeply on the trigger point in the middle of the shoulder blade (infraspinatus) |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder Pain and Disability Index (SPADI)
Time Frame: 6th week
|
SPADI is a 13 item Questionnaire to evaluate pain (5items) and disability (8 items) in shoulder joint.
The patient is instructed to choose the number that best describes their level of pain and extent of difficulty using the involved shoulder.
The pain scale is summed up to a total of 50 while the disability scale sums up to 80.
The total SPADI score is expressed as a percentage.
A score of 0 indicates best 100 indicates worst.
A higher score shows more disability.
|
6th week
|
|
Universal Goniometer (UG)
Time Frame: 6th week
|
Universal goniometer is tool in orthopedics used to precisely measure angles at joints. Goniometer demonstrates good intra-rater and inter-rater reliability when used consistently with proper technique. It will measure the ranges at shoulder joint (Abduction, Adduction, Flexion, Extension, Internal rotation, External rotation |
6th week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: summaya asim, MSPT(CP), Riphah International University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/25/0109
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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