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Clinical Trials/NCT05325255
NCT05325255RecruitingNot Applicable

Effect of Myofascial Release of Subscapularis Along With Shoulder Mobilization Versus Shoulder Mobilization Alone in Adhesive Capsulitis

Dow University of Health Sciences2 sites in 1 country70 target enrollmentStarted: April 26, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
70
Locations
2
Primary Endpoint
Change from baseline pain intensity on Numeric Pain Rating Scale in scores at 6th session (10 days)

Study Overview

Brief Summary

This randomized control trial aims to compare the effect of myofascial release of subscapularis along with shoulder mobilization VS mobilization alone among patients with adhesive capsulitis. The study will be conducted at physiotherapy outpatient department (OPD) of Sindh Institute of physical medicine and rehabilitation, and Dow University Ojha Campus, Karachi. According to study criteria, 70 patients with sub-acute adhesive capsulitis will be selected through a non-randomized purposive sampling technique by a consultant physician. After taking informed consent, participants will be randomly divided into 2 groups through the sealed envelope method. Both the groups will receive conventional treatment while Group 1 will be given an additional treatment of myofascial release of subscapularis through ischemic compression technique. Total 6 treatment sessions will be provided and assessment will be done at baseline and end of the 6th session.

Detailed Description

The sample size of 31 per group was determined using planning and specification software (PASS) version 15 software based on two independent sample t-test using 95%confidence interval and 80% power of the test. This sample was raised to 35 per group with 4 patients as drop out per group. Mean and standard deviation will be calculated for the quantitative variables while frequency and percentages will be calculated for qualitative variables. Inter-group comparison at baseline will be calculated using an independent sample t-test. The mean difference between both the techniques in terms of numeric pain rating scale (NPRS), range of motion (ROM), shoulder pain and disability index (SPADI), and pain pressure threshold(PPT) will be determined using Repeated measure 2-way ANOVA.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients aged between 40-65 years
  • •Diagnosed with sub-acute adhesive capsulitis
  • •Pain range of 3 to 8 on NPRS
  • •SPADI score of >40
  • •Presence of myofascial trigger point in subscapularis muscle

Exclusion Criteria

  • •History of fracture
  • •Rheumatoid arthritis
  • •Shoulder osteoarthritis
  • •Any malignancy
  • •Shoulder dislocation
  • •Subacute adhesive capsulitis with impingement syndrome

Arms & Interventions

Maitland mobilization alone group

Active Comparator

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Maitland mobilization (Other)

Maitland mobilization with myofascial trigger point release group

Experimental

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Ischemic Compression technique: on subscapularis trigger points for 90 secs thrice a week for 2 weeks.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Myofascial release of subscapularis (Other)

Maitland mobilization with myofascial trigger point release group

Experimental

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Ischemic Compression technique: on subscapularis trigger points for 90 secs thrice a week for 2 weeks.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Maitland mobilization (Other)

Maitland mobilization with myofascial trigger point release group

Experimental

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Ischemic Compression technique: on subscapularis trigger points for 90 secs thrice a week for 2 weeks.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Stretching exercises (Other)

Maitland mobilization with myofascial trigger point release group

Experimental

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Ischemic Compression technique: on subscapularis trigger points for 90 secs thrice a week for 2 weeks.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Cold pack (Other)

Maitland mobilization alone group

Active Comparator

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Stretching exercises (Other)

Maitland mobilization alone group

Active Comparator

Maitland technique: caudal, anteroposterior (AP), and posteroanterior (PA) glides 5 sets of 2-3 glides per second of Grade III and IV for 30 seconds with a rest interval of 30 second between sets.

Stretching exercises in direction of abduction, external rotation (ER), internal rotation (IR), and flexion. 6 repetitions of each stretch for 10 seconds Cold pack for 20 mins

Intervention: Cold pack (Other)

Outcomes

Primary Outcomes

Change from baseline pain intensity on Numeric Pain Rating Scale in scores at 6th session (10 days)

Time Frame: At baseline and after 6 sessions (10 days)

It will be use to assess pain intensity. It will be administered by simply asking the intensity of pain experienced in last 24 hours. The response of 0 represent no pain rather the responses between 1-3, 4-6, and 7-9 represents mild, moderate, and severe pain respectively. While 10 is the worst possible pain ever experienced by the person

Change from baseline joint range of motion on universal goniometer in degrees at 6th session (10 days)

Time Frame: At baseline and after 6 sessions (10 days)

It will be assessed by using standard universal goniometer and measured in degrees

change from baseline shoulder disability on Shoulder pain and disability index in percentage at 6th session (10 days)

Time Frame: At baseline and after 6 sessions (10 days)

Shoulder pain and disability index is used to assess shoulder disability. It consist of 13 questions i .e. 5 to assess pain and 8 to assess disability. Results will be calculated in percentage and higher results indicate increased disability. lower the percentage better will be the outcome.

Change from baseline pain pressure threshold on algometer in kilogram/centimeter2 at 6th session (10 days)

Time Frame: At baseline and after 6 sessions (10 days)

assessed through algometer which provide sustained pressure from 0.05Newton/second to 20 Newton/second. Results will be recorded in kilogram/centimeter2 and higher values indicate decrease sensitivity of myofascial trigger points

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Umama Abbasi

Principle Investigator

Dow University of Health Sciences

Study Sites (2)

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