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Virtual Reality Based Exercise Training Versus Mulligan Mobilization on Shoulder Posture and Function in Subacromial Impingement Syndrome

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Subacromial Impingement Syndrome

Treatments

Other: Virtual Reality
Other: Mulligan mobilization

Study type

Interventional

Funder types

Other

Identifiers

NCT07369934
Virtual reality and Mulligan M

Details and patient eligibility

About

The study will compare the effect of virtual reality based exercise training versus Mulligan mobilization in addition to exercise therapy added to both groups on shoulder posture and function in subacromial impingement syndrome.

Enrollment

74 estimated patients

Sex

All

Ages

30 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients will be referred from the orthopedic surgeon with a diagnosis of stage II SIS with the following criteria:

    1. Participants ranged in age from 30-50 years old.
    2. Participants are from non-athletes from the general population.
    3. Unilateral shoulder pain that is localized either anteriorly or laterally to the acromion. Pain that occurs or worsens when the affected shoulder is in flexion and/or abduction.
    4. Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and painful greater tuberosity of the humerus.
    5. BMI range 18.5- 29.9 Kg/m².

Exclusion criteria

  • 1) Patients who, during the previous three months, underwent shoulder physical treatment and/or an acute pain flare.

    2) Patients who have undergone surgeries for tendon repair. 3) Malignancy, epilepsy, pregnant women, and/or systemic conditions like chronic renal or liver failure.

    4) Mini-Mental State Examination test (MMSE) (< 24/30) to exclude cognitive impairment and/or significant vision impairment (if they couldn't read the introduction while wearing the Head Mounted Device (HMD).

    5) Corticosteroid injection during the last three months or used steroids chronically.

    6) Adhesive capsulitis, glenohumeral joint instability, Numbness or tingling of the upper limb, and/or full-thickness tear of the rotator cuff.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

74 participants in 2 patient groups

Virtual reality group
Active Comparator group
Treatment:
Other: Virtual Reality
Mulligan mobilization group
Active Comparator group
Treatment:
Other: Mulligan mobilization

Trial contacts and locations

1

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Central trial contact

Sara M Meselhy, Demonstrator; Afaf M Tahoon, lecturer

Data sourced from clinicaltrials.gov

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