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Cervical Unilateral Antero-posterior Mobilization and Thoracic Central Postro-anterior Mobilization in Treatment of Shoulder Impingement Syndrome

The Addition of Cervical Unilateral Antero-posterior Mobilization and Thoracic Central Postro-anterior Mobilization to Selected Therapeutic Exercise Program in Treatment of Shoulder Impingement Syndrome: A Randomized Clinical Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06349746
Enrollment
56
Registered
2024-04-05
Start date
2024-04-01
Completion date
2024-07-26
Last updated
2026-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Impingement

Brief summary

Shoulder impingement syndrome (SIS) is a complex, multi-factorial problem that is treated with a variety of different conservative options. The conservative option that has shown effectiveness is manual therapy of the cervical and thoracic spine

Detailed description

This study will be conducted to answer the following question: What is the effect of adding cervical and thoracic mobilization to selected therapeutic exercise Program on pain intensity, Pain-free shoulder flexion and scaption active ROM, muscle strength of external rotator and abductors, shoulder functional status in patients with Shoulder Impingement Syndrome

Interventions

OTHERtherapeutic exercises

One group received an exercise program that consisted of pain control, ROM, as well as education in scapular control, strengthening of muscles around the shoulder blades, and starting sensory-motor training. The program consisted of all exercises being performed in 3 sets of 15 repetitions. also, scapular stabilizing exercise were added

OTHERmobilization exercise

cervical unilateral antero-posterior mobilization and thoracic central postro-anterior mobilization

Sponsors

Egyptian Chinese University
Lead SponsorOTHER
Benha University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

patients and outcomes assessor will be masked about the grouping of the study

Intervention model description

Both groups underwent a physical therapy program; study group received additional cervical and thoracic mobilization. Outcomes included pain intensity, pain-free shoulder active range of motion (ROM) in scaption, flexion, abduction, internal and external rotation, muscle strength of external and internal rotators and abductors, and overall shoulder functional status.

Eligibility

Sex/Gender
MALE
Age
25 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

required at least three positive findings from five diagnostic tests for SIS (Hawkins-Kennedy test, Neer's test, painful arc, Resisted External Rotation test, Jobe's test) and persistent shoulder pain (anterolateral shoulder region) for 3 to 6 months, along with limitations in functional movements as Individuals who experienced painful restrictions in their ability to raise their shoulder (flexion, abduction, scaption) and had pain or limitations when performing functional movements such as reaching behind their back or behind their head. As well as subjects who willingly participated in the study and gave their consent for the research purposes.

Exclusion criteria

included adhesive capsulitis, radiologically confirmed grade III rotator cuff tears, calcific tendinitis, neurological or systemic disorders, cervical radiculopathy, prior shoulder surgery, recent corticosteroid injections, or recent physiotherapy within the previous three months. Patients complain from shoulder pain without pain on palpation, mobility limitations or pain during provocative tests, but complaining of abdominal tenderness on palpation were also excluded from this study.

Design outcomes

Primary

MeasureTime frameDescription
pain intensitypre intervention and after 6 weeks of interventionpain intensity will be measured by visual analogue scale
shoulder flexion and abduction range of motionpre intervention and after 6 weeks of interventionmeasurement of shoulder flexion and abduction range of motion applied by using digital goniometer
muscle strengthpre intervention and after 6 weeks of interventionshoulder flexors and external rotators muscle strength will be measured by dynamometer

Countries

Egypt

Contacts

PRINCIPAL_INVESTIGATORNoha Elserty

Benha University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026