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Effects of the Myofascial Arm Pull With and Without Active Release Technique in Adhesive Capsulitis

Effects of the Myofascial Arm Pull With and Without Active Release Technique on Pain, Range of Motion and Disability in Adhesive Capsulitis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06108843
Enrollment
38
Registered
2023-10-31
Start date
2023-05-08
Completion date
2024-01-31
Last updated
2023-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adhesive Capsulitis

Keywords

Adhesive Capsulitis, Active Release Technique, Myofacial Arm Pull Technique, Pain, Range of Motion

Brief summary

The aim of the study is to determine the effects of the myofascial arm pull with and without active release technique on pain, ROM and disability in adhesive capsulitis.

Detailed description

Adhesive capsulitis (frozen shoulder), a painful disorder caused by capsular inflammation that results in fibrosis and rigidity of the glenohumeral joint capsule, is characterized by a progressive loss of both active and passive glenohumeral movements. Frozen shoulder can be primary (also known as idiopathic) if there is no underlying cause of disease or it can be secondary. The term secondary frozen shoulder is associated with injury, trauma, cardiovascular diseases, hemiparesis, or diabetes.Active release technique and myofascial arm pull technique are both effective treatment options for patients with adhesive capsulitis. These techniques help to improve range of motion and reduce pain by releasing tension and adhesions in the affected area. Active release technique focuses on releasing tension and adhesions in the soft tissues surrounding the affected joint, while the Myofascial arm pull technique aims to improve range of motion by stretching the muscle and fascia in the affected area. By incorporating these techniques into a comprehensive treatment plan, patients of adhesive capsulitis can see significant improvement in their pain, range of motion and disability. Because the method of treatment is inexpensive, findings of this study could be beneficial in revision of the clinical protocols to manage the patients of adhesive capsulitis.

Interventions

OTHERMyofascial Arm Pull and Active Release Technique

Six weekly sessions of the treatment will be given over the course of four weeks. Baseline treatment includes Ultrasound for 10 minutes.

OTHERMyofacial Arm Pull

Six weekly sessions of the treatment will be given over the course of four weeks. Baseline treatment includes Ultrasound for 10 minutes.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

A participant in a single-blind study does not know which study group they are in, but the study doctor does.

Intervention model description

A type of intervention model describing a clinical trial in which two or more groups of participants receive different interventions.

Eligibility

Sex/Gender
ALL
Age
35 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Both Male and Female; mean age (35-60). * Case diagnosed with adhesive capsulitis, both primary and secondary origin. * Freezing stage of adhesive capsulitis. * Those with at least a 50% reduction in the range of motion (ROM).

Exclusion criteria

* History of shoulder surgery or manipulation under anesthesia, local corticosteroid injection administration to the affected shoulder within the last 3 months. * Neurological deficit affecting the shoulder functioning during daily activities. * Pathology of the shoulder joint other than adhesive capsulitis. * Pain or disorder of the cervical spine, elbow, wrist or hand. * Patients diagnosed with cancer

Design outcomes

Primary

MeasureTime frameDescription
Goniometer4 weekChanges from Baseline. Physical therapists use goniometry to objectively measure passive and active range of motion (ROM).
Shoulder Pain and disability index (SPADI)4 weekChanges from Baseline. The Shoulder Pain and Disability Index (SPADI) was developed to measure current shoulder pain and disability in an outpatient setting. The SPADI contains 13 items that assess two domains; a 5-item subscale that measures pain and an 8-item subscale that measures disability
Numeric Pain Rating Scale (NPRS)4 weekChanges from Baseline. The NPRS is a self-reported, or clinician administered, measurement tool The scale is typically set up on a horizontal or vertical line, ranges most commonly from 0-10. 0=No pain 1 to 4=Mild pain. 5 or 6=Moderate pain 7 to 10=Severe pain

Countries

Pakistan

Contacts

Primary ContactIMRAN AMJAD, PHD
imran.amjad@riphah.edu.pk03324390125
Backup ContactIMRAN AMJAD, PHD
051-5481826

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026