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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-08

Study Completion Date

2024-01-31

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Adhesive Capsulitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

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

Study Groups

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Myofascial arm pull technique and Active Release Technique

Participant will receive both Myofascial arm pull and active release technique along with Ultrasound therapy.

Group Type EXPERIMENTAL

Myofascial Arm Pull and Active Release Technique

Intervention Type OTHER

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

Myofascial arm pull technique

Participant will receive Myofascial arm pull along with ultrasound therapy.

Group Type ACTIVE_COMPARATOR

Myofacial Arm Pull

Intervention Type OTHER

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

Interventions

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Myofascial 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.

Intervention Type OTHER

Myofacial Arm Pull

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

Intervention Type OTHER

Eligibility Criteria

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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

Minimum Eligible Age

35 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No