NCT07800559

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
7mo left

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Study Progress10%
Sep 2026May 2027

First Submitted

Initial submission to the registry

August 29, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 2, 2026

Completed
8 days until next milestone

Study Start

First participant enrolled

September 10, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 10, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 10, 2027

Last Updated

September 2, 2026

Status Verified

August 1, 2026

Enrollment Period

8 months

First QC Date

August 29, 2026

Last Update Submit

August 29, 2026

Conditions

Keywords

Thoracic ManipulationInstrument-assisted Soft Tissue MobilizationShoulder Impingement Syndrome

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 COMPARATOR

Twenty patients with shoulder impingement syndrome will receive conventional physical therapy three times per week for 6 weeks

Other: conventional physical therapy

thoracic manibulation

EXPERIMENTAL

twenty patients with shoulder impingement syndrome will receive thoracic manibulation plus conventional physical therapy three times per week for 6 weeks

Other: conventional physical therapyOther: thoracic manibulation

nstrument assisted soft tissue mobilization

EXPERIMENTAL

twenty patients with shoulder impingement syndrome will receive conventional physical therapy and instrument-assisted soft tissue mobilization three times per week for 6 weeks

Other: conventional physical therapyOther: instrument assisted soft tissue mobilization

thoracic manipulation and instrument-assisted soft tissue mobilization.

EXPERIMENTAL

twenty 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

Other: conventional physical therapyOther: thoracic manibulationOther: instrument assisted soft tissue mobilizationOther: thoracic manipulation and instrument-assisted soft tissue mobilization

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.

conventional physical therapynstrument assisted soft tissue mobilizationthoracic manibulationthoracic manipulation and instrument-assisted soft tissue mobilization.

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.

thoracic manibulationthoracic manipulation and instrument-assisted soft tissue mobilization.

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

nstrument assisted soft tissue mobilizationthoracic manipulation and instrument-assisted soft tissue mobilization.

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

thoracic manipulation and instrument-assisted soft tissue mobilization.

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Central Study Contacts

Nabil mahmoud, professor

CONTACT

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
Model Details: Thoracic Manipulation and Instrument-assisted Soft Tissue Mobilization
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