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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05889065
Other study ID # FUI/CTR/2023/8
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 1, 2022
Est. completion date July 1, 2023

Study information

Verified date May 2023
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 32
Est. completion date July 1, 2023
Est. primary completion date June 15, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Procedure:
Conventional Physical Therapy
group A will receive conventional physical therapy including 10 ultrasound(1.5w/cm2 ,3 MHz continuous type, duration 10 minutes),hot packs (on affected region of shoulder for 10 minutes),shoulder ROM, stretching exercises, and joint mobilization five times per week for two weeks with 40 minutes duration of each session. Maitland mobilization will be given in supine position. · After giving glenohumeral joint distraction, caudal, dorsal, and ventral glides will be given at a rate of 2-3 oscillation/second for 1 to 2 minutes to patients. Grade I or II rhythmic oscillations will be applied in free range.
PNF techniques
In this group 20 repetitions of diagonal scapular pattern (anterior elevation and posterior depression, posterior elevation and anterior depression) with 20 seconds rest period will be given to subjects. PNF techniques of rhythmic initiation and repeated contractions will be used in all patterns, applied for 40 minutes.

Locations

Country Name City State
Pakistan Foundation University Islamabad Islamabad Federal

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shoulder Pain Shoulder Pain will be measured on the basis of visual analogue scale of 0-100mm. A higher score signifies greater pain. 2 weeks
Secondary Shoulder range of motion (ROM) Shoulder range of motion (ROM) will be measured through goniometer. A higher score signifies greater range. 2 weeks
Secondary Scapular mobility scapular mobility will be measured through lateral slide test (LSST) 2 weeks
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