Effects of lumbar mobilization techniques on lower cross syndrome
Effects of Lumber Sustained Natural Apophyseal Glides on Lower Cross Syndrome
NA · Riphah International University · NCT06707805
This study is testing if a specific back treatment can help people with lower cross syndrome feel less pain and move better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 36 (estimated) |
| Ages | 30 Years to 50 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Kotli, Azad Kashmir) |
| Trial ID | NCT06707805 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of sustained natural apophyseal glides (SNAGs) on individuals suffering from lower cross syndrome, a condition characterized by specific muscle imbalances leading to lower back pain and hypomobility. The research aims to assess how these mobilization techniques can correct biomechanical changes, such as hyperlordotic curves and anterior pelvic tilting, which are common in this syndrome. By focusing on noninvasive interventions, the study seeks to enhance patient well-being and movement quality through personalized physical therapy approaches. Participants will undergo traditional physical therapy alongside SNAGs to evaluate improvements in pain and mobility.
Who should consider this trial
Good fit: Ideal candidates are adults aged 30 to 50 who experience low back pain and exhibit symptoms of lower cross syndrome.
Not a fit: Patients with contraindications to spinal manipulation or those with significant musculoskeletal pathologies affecting the lower back may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly alleviate pain and improve mobility for patients with lower cross syndrome.
How similar studies have performed: While the specific application of SNAGs for lower cross syndrome may be novel, similar mobilization techniques have shown promise in other studies addressing spinal pain and dysfunction.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 30 to 50 years. * Both genders * Patient came with the complain of low back pain. * Participants had to present with pain and hypomobility due to lower cross syndrome * Participants had to meet the criteria for lower cross syndrome indicating tight hip flexors and erector spinae along with weak abdominals and glutei muscles * Participants with hyperlordotic curve due to lower cross syndrome * Participants presenting with anterior pelvic tilting greater than angle \>7-10 degrees * Willing to provide informed consent to participate in study Exclusion Criteria:Participants contraindicated to spinal manipulation * Musculoskeletal pathologies affecting the lower back, pelvis, hips, or lower extremities (e.g., herniated disc, lumbar radiculopathy, lumbar stenosis, hip labral tear). * Participants who had undergone any lumber or pelvic surgery, as it will affect sacroiliac joint mechanics. * Generalized inflammatory or infective connective tissue disorder * Pregnancy
Where this trial is running
Kotli, Azad Kashmir
- Orthopaedic hospital — Kotli, Azad Kashmir, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Asmar Fatima, MS OMPT — Riphah International University
- Study coordinator: Asmar Fatima, MS-OMPT
- Email: asmar.fatima@riphah.edu.pk
- Phone: 03336195644
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.
Conditions: Lower Cross Syndrome, pain, lumber SNGS