Effects of Scapular Proprioceptive Neuromuscular Facilitation on Pain and Range of Motion in Patients With Adhesive Capsulitis

Not Applicable

Active, not recruiting

• Conditions: Adhesive Capsulitis

• Registration Number: NCT05889065
• Lead Sponsor: Foundation University Islamabad

Brief Summary

The term ''frozen shoulder'' is defined as a clinical condition with restricted active and passive range of motion (ROM) in all directions, including flexion, abduction, and rotation.The objective of the study is to determine the effects of Scapular proprioceptive neuromuscular facilitation and conventional physical therapy among patients with adhesive capsulitis.The study will be a randomized controlled trial (single-blinded parallel study), consisting of 2 groups- interventional group A and interventional group B.Group A will be given conventional physical therapy and group B will be given conventional physical therapy alongwith scapular PNF.Scapular PNF exercises are not included in our routine PT treatment programs and there is limited literature related to the PNF techniques. These techniques help develop muscular strength and endurance, joint stability, mobility, neuromuscular control and coordination all of which are aimed at improving the overall functional ability of patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-08-01
• Status Verified: 2023-05
• Study First Submitted: 2023-05-25
• Study First Submitted QC: 2023-06-02
• Last Update Submitted: 2023-06-02
• Study First Posted: 2023-06-05
• Last Update Posted: 2023-06-05
• Primary Completion: 2023-06-15
• Study Completion: 2023-07-01

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

• Cases diagnosed with adhesive capsulitis, both primary and secondary origin.
• Stage two and stage three of adhesive capsulitis.
• Unilateral adhesive capsulitis.
• Both males and females of the age group 40 years and above.

Exclusion Criteria

• History of shoulder surgery or manipulation under anesthesia,
• Local corticosteroid injection administration to the affected shoulder within the last 3 months.
• Severe musculoskeletal, neurological and cardiovascular conditions.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Shoulder Pain	2 weeks	Shoulder Pain will be measured on the basis of visual analogue scale of 0-100mm. A higher score signifies greater pain.

Secondary Outcome Measures

Name	Time	Method
Shoulder range of motion (ROM)	2 weeks	Shoulder range of motion (ROM) will be measured through goniometer. A higher score signifies greater range.
Scapular mobility	2 weeks	scapular mobility will be measured through lateral slide test (LSST)

Trial Locations

Locations (1)

Foundation University Islamabad; 🇵🇰 Islamabad, Federal, Pakistan