The Effect of Myofascial Release in Patients With Subacromial Impingement Syndrome Randomized Controlled Trial
Myofascial Release
Shoulder Injuries+2
+ Joint Diseases
+ Musculoskeletal Diseases
Treatment Study
Summary
Study start date: January 11, 2024
Actual date on which the first participant was enrolled.Shoulder pain, especially due to rotator cuff issues, is a common problem that affects many people, often limiting their ability to work, enjoy hobbies, or participate in sports. This study focuses on understanding how effective a technique called myofascial release is in helping people with rotator cuff tendinopathy, a condition where the tendons in the shoulder become irritated or damaged. Myofascial release is a hands-on therapy that involves applying gentle pressure to relieve tension in the connective tissues. This study aims to see if adding this technique to standard shoulder exercises and treatments can improve shoulder function and reduce pain, potentially offering a better quality of life for those affected by this condition. In this study, participants are divided into two groups. One group receives standard treatment, which includes exercises to strengthen shoulder muscles, improve range of motion, and ice application to reduce swelling. The other group receives the same treatment but with the addition of myofascial release therapy. Each participant attends two sessions per week for one month, with each session lasting between 30 to 45 minutes. Independent physical therapists assess all participants using various scales to measure pain, shoulder movement, and psychological distress, ensuring a thorough evaluation of the treatment's effectiveness. This study is designed to compare the outcomes of the two groups to determine the added benefit of myofascial release in managing shoulder pain.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.36 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 20 to 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location