Effects Of Gong's Versus Mulligan Mobilization In Patients With Adhesive Capsulitis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-50
SponsorRiphah International University

About this trial

A Randomized Clinical Trial will be conducted at DHQ hospital kasur,BIT hospital kasur,Arif memorial hospital Lahore.Pre-diagnosed patients will be reassessed by applying (Shoulder Shrug Sign, Hand to neck, Hand to scapula, Hand to opposite scapula,Hand to back,Capsular pattern movement restriction)Plus all other special tests will be applied to confirm that symptoms are not due to other shoulder pathologies but are due to just adhesive capsulitis then through consecutive sampling technique on 60 patients they will be allocated using computer generated sampling(random number table) into Group A and Group B.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 40 to 50 years

Both male and female

Pre-diagnosed Unilateral Primary Frozen shoulder patients

Prediagnosed Stage 3(Frozen phase) patients(27)

Disqualifiers

Patients with previous surgery in the shoulder joint

History of recent fracture or severe trauma to the shoulder

Diagnosed instability or previous history of dislocation

Systemic inflammatory conditions(e.g.rheumatoid arthritis)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Gong's Mobilization Technique

    Other intervention

    The therapist will push the scapula of the affected side in a posterior to anterior direction with one hand, and pushed the humeral head in an anterior to posterior direction parallel to joint plane with the other hand.

  • Mulligan Mobilization Technique

    Other intervention

    Mulligan Mobilization Technique

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Gong's Technique GroupExperimental treatment 1 intervention
Group B: Mulligan MobilizationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Level of Pain

Numeric Pain Rating Scale

Time frame
Pre & Post 6 weeks
2

Range of Motion

Goniometer

Time frame
Pre & Post 6 weeks
3

Functional Disability

Shoulder Pain and Disability Index

Time frame
Pre & Post 6 weeks
4

Quality of Life Level

Sort Form Survey-36

Time frame
Pre & Post 6 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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