Actively Recruiting
Comparative Effects of Eldoa With and Without Muscle Energy Technique on Pain, Range of Motion and Functional Disability in Patient With Quadratus Lumborum Syndrome
Led by Riphah International University ยท Updated on 2024-12-13
62
Participants Needed
1
Research Sites
5 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the effects of Pilates exercises with and without whole body vibration on posture, pain, and disability in young adults with upper cross syndrome. The study focuses on addressing posture issues like rounded shoulder posture, which is common due to prolonged sitting and technology use. Researchers will evaluate different exercise programs to determine if adding whole body vibration to Pilates exercises influences pain, posture, and disability outcomes in this population. Participants will be randomly assigned to one of two groups: one group will receive a Pilates exercise program combined with whole body vibration, and the other group will receive a traditional physical therapy program including stretching, strengthening, and postural correction exercises. Both groups will have sessions twice a week for four consecutive weeks. Before exercise sessions, hot packs will be applied for 15 to 20 minutes. The Pilates with whole body vibration group and the traditional therapy group will both complete sessions lasting about 55 minutes to one hour. During the study, participants will be assessed at baseline and after four weeks using measures such as the Numeric Pain Rating Scale, Universal Goniometer for range of motion, and the Modified Oswestry Disability Index for functional disability. Data will be analyzed to compare changes within and between groups. The trial includes detailed evaluations of posture, pain, and function to understand the benefits of the interventions. Participants will be monitored throughout the study period of six weeks.
CONDITIONS
Brief Title
Comparative Effects of Eloda With/Without Muscle Energy Technique in Patient With Quadratus Lumborum Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age group between 18 to 45 years
- Both gender male and female
- Individuals with mechanical lower back pain
- Active trigger point in the quadratus lumborum muscle
- No previous history of accidents
You will not qualify if you...
- Acute muscular injuries
- Localized or systemic infections
- Lumbar disc herniation
- Spinal abnormalities or any prior history of spinal issues
- Use of anticoagulants and bleeding disorders
- Psychiatric conditions that would make it difficult to provide consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants receive either a Pilates exercise program combined with whole body vibration or a traditional physical therapy program including stretching, strengthening, and postural correction exercises.
2 sessions per week for 4 weeks (in-person)
Duration - 6 weeks
Participants' pain, range of motion, and functional disability are assessed after treatment.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Muhammad Sulman
Sialkot, Punjab Province, Pakistan, 51310
Actively Recruiting
Research Team
I
Imran Amjad
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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