Posterior Oblique Sling Strengthening for Gait Improvement in Young Adults
Group A myofascial technique
+ Group B posterior sling exercises
Treatment Study
Summary
Study start date: January 7, 2025
Actual date on which the first participant was enrolled.This study focuses on improving movement and stability in young adults aged 20 to 30 by strengthening a group of muscles known as the posterior oblique sling. This muscle group includes the latissimus dorsi, gluteus maximus, and thoracolumbar fascia, which are important for stabilizing the lower back and pelvis during movement. Many young people spend a lot of time sitting, which can lead to tightness in these muscles, affecting their ability to walk efficiently and increasing the risk of back pain. By addressing these issues through targeted exercises, the study aims to improve movement patterns, reduce pain, and enhance overall quality of life. Participants in the study will engage in various exercises designed to relieve tightness and strengthen the posterior oblique sling. Techniques such as Muscle Energy Techniques, dynamic stretching, and myofascial release will be used to increase muscle flexibility and mobility. Functional exercises like resisted trunk rotation and specific core strengthening moves will help improve stability and coordination. These exercises aim to restore proper movement and reduce symptoms of chronic low back pain by addressing muscle imbalances and improving gait mechanics. The study will assess how these interventions impact participants' movement quality and back health.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.46 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 18 to 30 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
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
Rawal Institute of Rehabilitation & Health Sciences (RIRH) & Rawal General & Dental Hospital. (RG&DH)
Islamabad, PakistanOpen Rawal Institute of Rehabilitation & Health Sciences (RIRH) & Rawal General & Dental Hospital. (RG&DH) in Google Maps