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Not yet recruiting NCT06618443

Scapular Mobilization With Arm Movement in Patients With Adhesive Capsulitis.

No phase Interventional Shoulder Adhesive Capsulitis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Scapular mobilization with movement.
Who it may be relevant to
Registry conditions: Shoulder Adhesive Capsulitis. Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Scapular Mobilization With Arm Movement on Shoulder Pain and Range of Motion and Disability in Older Adults With Adhesive Capsulitis.

Overview

50 patients with shoulder adhesive capsulitis were admitted. the patients will receive scapular mobilization (downward or upward mobilization) associated with arm movements. The percentage of improvement in shoulder ROM of flexion, abduction, and external rotation; and decrease in shoulder pain and disability index (SPADI).

Interventions

  • Other Scapular mobilization with movement
    The treatment consisted of scapular mobilization with arm movement in all directions for 15 min/session for 3 sessions/week for 4 weeks. Scapular mobilization included scapular upward glide and downward glid. Scapular upward glide was performed with shoulder adduction and extension, while scapular downward glide was performed with shoulder abduction and flexion.

Primary outcome measures

  • Shoulder Pain and Disability Index (SPADI) [Time frame: 3 months]
  • Shoulder range of motion of flexion, abduction, and external rotation [Time frame: 3 months]
  • Scapular dyskinesis [Time frame: 3 months]
  • Electromyography [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • The existence of unilateral adhesive capsulitis (stage II) with incapability of the participant to raise the arm more than 100 degrees in the plane of the scapula

Exclusion criteria

  • The presence of any shoulder problem contraindicated for performing exercises to the shoulder joint, such as active inflammatory disease, cancer, active infection, recent subluxations or dislocations, fractures, and surgeries near the shoulder region.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06618443 · BNS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗