Frozen Shoulder (Scapular Mobilization Versus Scapular PNF)

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Cairo University (CU)

Status

Not yet enrolling

Conditions

Scapular Mobilization
Frozen Shoulder
Scapular Proprioceptive Neuromuscular Facilitation

Treatments

Other: Group A SCAPULAR MOBILIZATION

Study type

Interventional

Funder types

Other

Identifiers

NCT06201468
Frozen shoulder

Details and patient eligibility

About

This study will be conducted to examine and compare the effects of SM versus SPNF on shoulder pain, ROM and functional disabilities in patients with frozen shoulder.

Full description

This study will be conducted to examine and compare the effects of SM versus SPNF on shoulder pain, ROM and functional disabilities in patients with frozen shoulder.

Enrollment

42 estimated patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All the patients refferd from orthopaedic surgeon with diagnosis of adhesive capsulitis. Patients will be included in this study if they fulfil the following criteria
  1. Case diagnosed with adhesive capsulitis, both primary and secondary.
  2. Both males and females of the age group 40 to 60 years.
  3. Limited active and passive movement of the shoulder joint movements, as well as difficulties with ADLs.

4- The onset of symptoms between 3 to 12 months. 5. Unilateral adhesive capsulitis.

Exclusion criteria

    1. History of shoulder surgery or manipulation under anaesthesia, local corticosteroid injection administration to the affected shoulder within the last 6 months, 2. Neurological deficit affecting the shoulder function during daily activities, 3. Pathology of the shoulder joint other than adhesive capsulitis including rotator cuff tear, tendonitis at the shoulder and neck region, malignancies, history of trauma or accidental injuries of the upper limb.

    4- Other pathological conditions including, a history of stroke, history of mastectomy and coronary artery bypass grafting (CABG).

    1. Rheumatoid arthritis, osteoporosis, or disorders of the cervical spine, elbow, wrist or hand.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

42 participants in 2 patient groups

group A
Experimental group
Description:
Group A (n = 21): will receive scapular mobilization combined with mobilization with movement (MWM) and capsular stretch for 4 weeks. Mulligan Mobilization with Movement for peripheral joints combines sustained manual application of 'gliding' force to a joint, with the aim of repositioning the positional faults with concurrent physiological motion of the joint, either performed actively by the subject or passively by the therapist
Treatment:
Other: Group A SCAPULAR MOBILIZATION
group B
Experimental group
Description:
Group B (n = 21): will receive scapular proprioceptive neuromuscular facilitation combined with (MWM) and capsular stretch for 4 weeks. Scapular PNF incorporates functional or diagonal patterns (anterior elevation - posterior depression and posterior elevation - anterior depression) for performing the exercises and can be used to stretch or strengthen the muscles selectively. These techniques help the muscles to relearn the normal timing of recruitment and the amount of activation to sustain the balance between different groups of muscles
Treatment:
Other: Group A SCAPULAR MOBILIZATION

Trial contacts and locations

1

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Central trial contact

Enas F Youssef, PhD; Mohamed M Elmorsy

Data sourced from clinicaltrials.gov

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