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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06404814
Other study ID # MSRSW/Batch-Fall22/707
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date September 30, 2024

Study information

Verified date May 2024
Source Superior University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study focus on the rehabilitation of patients with frozen shoulder through a manual technique called "Spencer MET".The purpose of this approach is to reduce the pain and improve the ROM and quality of life.


Description:

By comparing the effectiveness of functional electrical stimulation versus the Spencer technique in patients with adhesive capsuilitis is to determine which treatment approach will yields better outcomes in order to reduce the detrimental effects of disease process.Spencer METs consist of series of seven steps taken in order to decrease pain and stiffness in sholder regiegionn.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 32
Est. completion date September 30, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: - Patients with diabetic frozen shoulder - Patients having frozen shoulder after stroke - Subjects having stiff shoulder for at least 3 months - Subjects with bilateral/unilateral frozen shoulder - Subjects with idiopathic frozen shoulder Exclusion Criteria: - Bone fracture within past 12 weeks - Patients with hyper mobile joints - Subjects with Rotator cuff pathology - Dislocated shoulder - Subjects who had shoulder arthroplasty

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Transcutaneous electrical nerve stimulation (TENS)
(TENS) is a method of pain relief involving the use of a mild electrical current
Diagnostic Test:
Muscle Energy Technique
n Spencer's technique, there are seven steps as follows: shoulder extension along with elbow flexion, shoulder flexion with elbow extension, circumduction with compression, circumduction with distraction, shoulder abduction and internal rotation with elbow flexion, shoulder adduction and external rotation with elbow

Locations

Country Name City State
Pakistan Johar pain relief center Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Superior University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale (VAS): It is tool widely used to measure the intensity of pain and discomfort.VAS effectively used in randomized controlled trials for outcome measures,consisting of 10 cm straight line from 0 to 10.0 represents "No pain" and 10 represent "Worst pain". Patients can mark their severity of pain. 12 Months
Primary Goniometer Goniometer is instrument used to measure the range of motion of a joint. 12 months
See also
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Completed NCT06064396 - Effects of Gong's Mobilization With and Without Stecco Fascial Therapy in Patients With Adhesive Capsulitis N/A
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Recruiting NCT04653636 - MRI and Clinical Predictive Factors of the Response to Arthrographic Distension in Severe Capsulitis