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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-50
SponsorCairo University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants ranged in age from 30-50 years old.

Participants are from non-athletes from the general population.

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.

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.

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality

    Other intervention

    Fully immersive virtual reality mounted headset will be used

  • Mulligan mobilization

    Other intervention

    posterolateral shoulder Mulligan mobilization with movement (MWM) will be used

Treatment groups

74 Participants
are divided into 2 treatment groups
Group A: Virtual reality groupActive comparator 1 intervention
Group B: Mulligan mobilization groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity during shoulder elevation

It will be measured using the Numerical Pain Rating Scale (NPRS)

Time frame
pain intensity at the start of session 1 to the end of 1 month of treatment
2

Shoulder function

The Shoulder Pain and Disability Index (SPADI) will be used to measure the shoulder function.

Time frame
shoulder function at the start of session 1 to the end of 1 month of treatment
3

Shoulder flexion range of motion

The Clinometer Application will be used to measure it.

Time frame
shoulder flexion at the start of session 1 to the end of 1 month of treatment
4

Shoulder abduction range of motion

The Clinometer Application will be used to measure it.

Time frame
shoulder abduction at the start of session 1 to the end of 1 month of treatment

Secondary outcomes

1

Patients' enjoyment

A 7-point likert scale will be used to the evaluate the level of the patients' enjoyment at the end of the last session.

Time frame
It will be evaluated at the end of the last session (after 1 month)
2

patients' adherence to treatment sessions

patients' numbers of attended sessions will be calculated at the end of 1 month of treatment.

Time frame
patients' adherence at the start of session 1 to the end of 1 month of treatment

Other outcomes

Sponsors and contacts

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