The Combined Effect of Thoracic Manipulation and Instrument-assisted Soft Tissue Mobilization in Patients With Shoulder Impingement Syndrome
SIS
1 other identifier
interventional
80
0 countries
N/A
Brief Summary
This study will be conducted to investigate the combined effect of thoracic manipulation and instrument-assisted soft tissue mobilization in patients with shoulder impingement syndrome
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 29, 2026
CompletedFirst Posted
Study publicly available on registry
September 2, 2026
CompletedStudy Start
First participant enrolled
September 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 10, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 10, 2027
September 2, 2026
August 1, 2026
8 months
August 29, 2026
August 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
upper limb disability
Disabilities of the arm, shoulder and hand (Quick DASH) questionnaire will be used toassess upper limb diability.the QuickDASH only contains 11 items .It is a questionnaire that measures an individual's ability to complete tasks, absorb forces, and severity of symptoms.The QuickDASH tool uses a 5-point Likert scale from which the patient can select an appropriate number corresponding to his/her severity/function level.The QuickDASH outcome measure is designed to be used on patients presenting with one or more disabilities of the arm, shoulder, and hand. Scoring with 100 is more severe disability, and zero mean no disability.
up to six weeks
Secondary Outcomes (5)
pain intensity
up to 6 weeks
shoulder range of motion
up to six weeks
shoulder proprioception (joint position error)
up to six weeks
life disability
up to six weeks
pressure pain threshold
up to six weeks
Study Arms (4)
conventional physical therapy
ACTIVE COMPARATORTwenty patients with shoulder impingement syndrome will receive conventional physical therapy three times per week for 6 weeks
thoracic manibulation
EXPERIMENTALtwenty patients with shoulder impingement syndrome will receive thoracic manibulation plus conventional physical therapy three times per week for 6 weeks
nstrument assisted soft tissue mobilization
EXPERIMENTALtwenty patients with shoulder impingement syndrome will receive conventional physical therapy and instrument-assisted soft tissue mobilization three times per week for 6 weeks
thoracic manipulation and instrument-assisted soft tissue mobilization.
EXPERIMENTALtwenty patients with shoulder impingement syndrome will receive thoracic manipulation + instrument-assisted soft tissue mobilization. The conventional physical therapy three times per week for 6 weeks
Interventions
the patients will receive conventional physical therapy in the form of transcutaneous electrical nerve stimulation, ultrasound, and therapeutic exercise. The exercise includes range of motion exercises, stretching, scapular stabilization exercises, and rotator cuff strengthening.
With the participant in a prone position, the therapist will apply a high-velocity, short-lever, posterior-to-anterior (P-A) thrust. The thrust will be directed toward the spinous or transverse processes of the hypomobile thoracic vertebrae. Thoracic thrust manipulation demonstrated to manipulate specific thoracic segment mainly the mid-thoracic, plus conventional physical therapy.
The IASTM technique will be performed for 20 seconds parallel to the muscle fibers, followed by 20 seconds perpendicular to the muscle fibers, with the instrument held at a 45° angle to the skin. The beveled side of the M2T blade will be in contact with the skin. Stroke pressure and speed will be modified according to the participant's tolerance to avoid causing pain and according to the depth of the treated muscle plus conventional physical therapy.The technique will be applied to the pectoral muscles, shoulder rotator cuff musculature, and periscapular musculature, including the upper, middle, and lower fibers of the trapezius, rhomboids major and minor, teres major, and latissimus dorsi
the patients will receive The IASTM technique will be performed for 20 seconds parallel to the muscle fibers followed by 20 seconds perpendicular to the muscle fibers, with the instrument held at a 45° angle to the skin plus thoracic manibulation in which the therapist will apply a high-velocity, short-lever, posterior-to-anterior (P-A) thrust. The thrust will be directed toward the spinous or transverse processes of the hypomobile thoracic vertebrae. Thoracic thrust manipulation demonstrated to manipulate specific thoracic segments, mainly the mid-thoracic, plus conventional physical therapy. finally, the pateitns will recieve conventional physical therapy
Eligibility Criteria
You may qualify if:
- Patients with shoulder impingement syndrome from both genders their age from 18-55 years.
- History of shoulder pain for one month.
- Positive Neer's impingement test and Hawkin's Kennedy test.
- Painful arc sign.
You may not qualify if:
- History of Shoulder girdle fracture, dislocation and surgery
- Diagnosed with frozen shoulder or rotator cuff tear
- History of cervicobrachial pain
- Any neuromuscular pain in upper limb and use of corticosteroids or pain subsiding medication.
- Inflammatory arthropathies (e.g., rheumatoid arthritis, ankylosing spondylitis).
- Fracture or malignancy in the shoulder region
- Contraindications to manual therapy or thoracic manipulation (e.g., osteoporosis, spinal cord compression, vertebral artery insufficiency).
- Contraindications to IASTM (e.g., open wounds, skin infections, bleeding disorders, anticoagulant therapy).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : nabil mahmoud ismail
Study Record Dates
First Submitted
August 29, 2026
First Posted
September 2, 2026
Study Start
September 10, 2026
Primary Completion (Estimated)
May 10, 2027
Study Completion (Estimated)
May 10, 2027
Last Updated
September 2, 2026
Record last verified: 2026-08