- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07403409
Scapular Repeated Contractions Facilitation Versus Hold-relax Techniques in Patients With Adhesive Capsulitis
February 4, 2026 updated by: Riphah International University
Effects of Scapular Repeated Contractions Facilitation Versus Hold-relax Techniques on Pain, Range of Motion and Functional Disability in Patients With Adhesive Capsulitis
The study was conducted to determine the effects of scapular repeated contractions facilitation versus hold-relax techniques on pain, range of motion and functional disability in patients with adhesive capsulitis
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
66
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab Province
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Dhok Gujra, Punjab Province, Pakistan, 50700
- Rasool Medical Complex Gujrat
-
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Diagnosed stage 2 of Adhesive Capsulitis (>4-12 months)
- Difficulties in 2 or more movements: external rotation, abduction, flexion or internal rotation presenting limitation of more than 30 degrees
- Patients having diagnosed Diabetes Mellitus type 2
- Capsular pattern of restriction
- Unilateral involvement of the shoulder
- Patients who are not taking any pain killer
Exclusion Criteria:
- Surgical history of affected shoulder
- History of trauma or fracture in affected shoulder
- Cervical neuropathy or any other disorders of cervical spine, elbow and wrist
- Any Neurological disorders such as stroke or parkinsonism
- Any systemic disease such as rheumatoid arthritis, osteoporosis and malignancies in shoulder region
- Intra-articular injection
- Open wound or skin infection
- Manipulation under anesthesia
- Recurrent dislocation or subluxation
- Shoulder injuries such as rotator cuff tear, or tendon calcification
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Scapular Repeated Contraction Facilitation Technique
|
Repeated contraction facilitation on scapula in two diagonal patterns (D1&D2) were performed .D1 consisted of anterior elevation and posterior depression and D2 consisted of posterior elevation and anterior depression.
Isotonic contraction of muscles against the resistance throughout the active ROM was performed.3
sets of 10 repetitions were performed with 20 seconds of rest interval.
Moist heat pack for 15-20 mins Therapeutic Ultrasound at 1MHz for 8-10 mins in continuous mode with the intensity of 1.5W/cm2 Active Assisted Shoulder for abduction, flexion, internal rotation and external rotation with 3 sets of 15 repetitions 4days/week for 4 weeks Wall slides, Finger ladder exercises, Wand exercises and home exercises were performed.3x15
repetitions with 2 min rest interval for 4 sessions per week for four weeks for each exercise Maitland Glenohumeral Joint Mobilization with 2-3 oscillations per second for 30 seconds for 5 sets 4 times a week in caudal and posteroanterior direction was applied for 4 weeks.
|
|
Active Comparator: Scapular Hold-Relax Technique
|
Moist heat pack for 15-20 mins Therapeutic Ultrasound at 1MHz for 8-10 mins in continuous mode with the intensity of 1.5W/cm2 Active Assisted Shoulder for abduction, flexion, internal rotation and external rotation with 3 sets of 15 repetitions 4days/week for 4 weeks Wall slides, Finger ladder exercises, Wand exercises and home exercises were performed.3x15
repetitions with 2 min rest interval for 4 sessions per week for four weeks for each exercise Maitland Glenohumeral Joint Mobilization with 2-3 oscillations per second for 30 seconds for 5 sets 4 times a week in caudal and posteroanterior direction was applied for 4 weeks.
Hold -Relax on scapula in two diagonal patterns (D1&D2) were performed .D1 consisted of anterior elevation and posterior depression and D2 consisted of posterior elevation and anterior depression in which restricted muscles were contracted isometrically with 5 sec hold followed by relaxation into new range .3
sets of 10 repetitions were performed with 20 seconds of rest interval.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: At base line and end of 4 weeks
|
Patient level of pain was assessed using this scale.
This scale ranges from 0 to 10. 0 indicates "no pain" ,1- 3 indicates mild pain ,4-6 indicates moderate pain and 7-10 indicates "worst pain".
NPRS have shown high test-retest reliability (r = 0.96 and 0.95, respectively) MCID value of NPRS is 2-3
|
At base line and end of 4 weeks
|
|
Shoulder Pain And Disability Index
Time Frame: from baseline to end of 4 weeks
|
SPADI was used to assess functional disability.
It has 13 items, with 5 items for pain and 8 items for disability
|
from baseline to end of 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ROM shoulder flexion
Time Frame: 4th week
|
changes from baseline ROM of shoulder flexion was taken
|
4th week
|
|
ROM shoulder abduction
Time Frame: 4th week
|
changes from baseline ROM of shoulder was taken
|
4th week
|
|
ROM shoulder external rotation
Time Frame: 4th week
|
changes from baseline ROM of shoulder external rotation was taken
|
4th week
|
|
ROM shoulder internal rotation
Time Frame: 4th week
|
changes from baseline ROM of shoulder internal rotation was taken
|
4th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ameena Amjad, Ph.D, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Joshi D, Chitra J. Effect of scapular proprioceptive neuromuscular facilitation on shoulder pain, range of motion, and upper extremity function in hemiplegic patients: A randomized controlled trial. Indian Journal of Health Sciences and Biomedical Research KLEU. 2017;10(3):276-82.
- Chitra J, Joshi D. Effect of scapular hold-relax technique on shoulder pain in hemiplegic subjects: A randomized controlled trial. Physiotherapy-The Journal of Indian Association of Physiotherapists. 2017;11(2):49-52.
- Mishra N, Mishra A, Charaniya P. Effect of scapular proprioceptive neuromuscular facilitation on pain and disability in patients with adhesive capsulitis. Int J Yogic Hum Mov Sports Sciences. 2019;4(1):995-1000.
- Saeed M, Hafeez S, Asad F, Haider W, Nawaz S, Kocub S. Comparison of scapular proprioceptive neuromuscular facilitation and myofascial release techniques on pain and function in scapular dyskinesia associated with adhesive capsulitis: Scapular dyskinesia associated with adhesive capsulitis. Pakistan BioMedical Journal. 2022:123-7.
- Bhavika PG, Vinosh Kumar P. Effect of Scapular Proprioceptive Neuromuscular Facilitation versus Scapular Mobilization on Pain and function in adhesive capsulitis-A Pragmatic Randomized Clinical Trial. INTI JOURNAL. 2023;2023(64):1-6.
- Akgüller T, Akbaba YA, Taşkıran H. The effect of scapular proprioceptive neuromuscular facilitation techniques on pain and functionality in patients with subacromial impingement syndrome: a randomized controlled trial. Physikalische Medizin, Rehabilitationsmedizin, Kurortmedizin. 2023;33(03):149-61.
- Shaikh SB, Ganvir SS. Effect of 4 Weeks of Scapular Proprioceptive Neuromuscular Facilitation on Scapular Alignment and Upper Extremity Motor Performance in Patients with Stroke: A Repeated Measure Design. Medical Journal of Dr DY Patil Vidyapeeth. 2023;16(Suppl 2):S228-S34.
- Ragapriyaa R, Kamalakannan M, Anitha A, Ramana K. Effect of Scapular Clock Exercise Versus Scapular PNF Exercise on Pain and ROM for Anterior Capsular Stiffness of Shoulder Joint. Indian Journal of Physiotherapy & Occupational Therapy. 2024;18.
- Cellatoğlu H, Kaygısız BB. Effect of proprioceptive neuromuscular facilitation (PNF) technique on posture, balance and gait characteristics of older adults with scapular dyskinesis: a randomized controlled trial. PeerJ. 2025;13:e19718.
- Butt MS, Tanveer F. Effects of scapular proprioceptive neuromuscular facilitation techniques in addition to routine physical therapy on clinical outcomes in patients with adhesive capsulitis: A randomized controlled trial. The Healer Journal of Physiotherapy and Rehabilitation Sciences. 2022;2(1):78-87.
- Ghias S, Saeed H, Ahmed M, Faisal M, Solangi TA, Asim HAB, et al. Effectiveness of PNF Pattern in Regular Physical Therapy Sessions on Functional Mobility in Frozen Shoulder: PNF Pattern in Frozen Shoulder Therapy. THE THERAPIST (Journal of Therapies & Rehabilitation Sciences). 2024:46-50.
- Lin P, Yang M, Huang D, Lin H, Wang J, Zhong C, et al. Effect of proprioceptive neuromuscular facilitation technique on the treatment of frozen shoulder: a pilot randomized controlled trial. BMC musculoskeletal disorders. 2022;23(1):367
- Zhang EJX, Lam YX, Lim WSR, Lie DTT. Effect of proprioceptive neuromuscular facilitation on efficacy and pain relief for symptomatic shoulder conditions: a meta-analysis. Journal of Orthopaedic Reports. 2025;4(1):100541.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 18, 2025
Primary Completion (Actual)
May 31, 2025
Study Completion (Actual)
October 30, 2025
Study Registration Dates
First Submitted
February 4, 2026
First Submitted That Met QC Criteria
February 4, 2026
First Posted (Actual)
February 11, 2026
Study Record Updates
Last Update Posted (Actual)
February 11, 2026
Last Update Submitted That Met QC Criteria
February 4, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/24/0196
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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