Comparing two techniques for treating Levator Scapulae Syndrome
Effects of Post-Isometric Relaxation Versus Static Stretching on Pain, Range of Motion, Disability and Muscle Length in Patients With Levator Scapulae Syndrome.
This study is testing whether a new way of relaxing muscles or a traditional stretching method works better for people with Levator Scapulae Syndrome to help reduce pain and improve movement.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 42 (estimated) |
| Ages | 24 Years to 59 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Daska Kalan, Punjab Province) |
| Trial ID | NCT06686290 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of Post-Isometric Relaxation versus Static Stretching in patients suffering from Levator Scapulae Syndrome. Participants will be randomly assigned to one of two groups, with Group A receiving Post-Isometric Relaxation and Group B undergoing Static Stretching. Each treatment will be administered three times a week for four weeks, with outcomes measured in terms of pain, range of motion, disability, and muscle length. Data analysis will be conducted using SPSS software to determine the effectiveness of each technique.
Who should consider this trial
Good fit: Ideal candidates are males and females aged 24-59 with neck and scapular pain lasting at least three months and a pain score greater than 3.
Not a fit: Patients with conditions such as neuropathies, vertebral fractures, or fibromyalgia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with a more effective treatment option for alleviating pain and improving mobility associated with Levator Scapulae Syndrome.
How similar studies have performed: While similar approaches have been explored, this specific comparison of Post-Isometric Relaxation and Static Stretching in this patient population is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both males and females. * Age range of 24-59 years. * Neck and medial border scapular pain for at least 3 months. * NPRS score greater than 3. * Reduced side flexion and rotation of neck. * Symptoms persisted for at least 3 months. * Positive levator scapulae length test. * Have suffered from myofascial pain Exclusion Criteria: * Neuropathies. * Vertebral fractures. * Pregnancy. * Fibromyalgia. * Cancer. * Traumatic neck injury. * Previous cognitive and functional disorders. * Coagulopathy(
Where this trial is running
Daska Kalan, Punjab Province
- Tehsil Headquarter Hospital Daska — Daska Kalan, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Muhammad Hassan, MSPT — Riphah International University
- Study coordinator: Imran Amjad, Phd PT
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.