Effects of neural flossing and PNF on lumbar radiculopathy
Effects of Neural Flossing With and Without Proprioceptive Neuromuscular Facilitation on Pain, Range of Motion and Disability in Patients With Lumbar Radiculopathy.
This study is testing whether adding a special movement technique to neural flossing can help people with lower back nerve pain feel better and move more easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 22 (estimated) |
| Ages | 35 Years to 50 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Gujrāt, Punjab) |
| Trial ID | NCT05922228 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effects of neural flossing, both with and without the addition of proprioceptive neuromuscular facilitation (PNF), on pain, range of motion, and disability in patients suffering from lumbar radiculopathy. Participants will be divided into two groups: one receiving only neural flossing and the other receiving neural flossing combined with PNF. The study seeks to determine whether the addition of PNF provides any significant benefits over neural flossing alone in improving patient outcomes. The trial will focus on measuring changes in pain levels, mobility, and overall disability.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 35-50 years with a pain intensity of 4 out of 10 on a numeric pain rating scale and a history of radiculopathy lasting more than three weeks.
Not a fit: Patients with cognitive impairments, those using pain-modulating medications, or individuals with comorbidities may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a new therapeutic approach to alleviate pain and improve mobility in patients with lumbar radiculopathy.
How similar studies have performed: Previous studies have suggested that combining neural flossing with conventional physiotherapy may enhance treatment outcomes, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 35-50 years. * Both males and females. * Pain intensity is 4 out of 10 on numeric pain rating scale. * History of radiculopathy for more than 3 weeks. * Pain radiating below to knee. Exclusion Criteria: * Cognitive impairment. * Using pain modulating medicines. * Patients with comorbidities. * Pain radiating above to knee.
Where this trial is running
Gujrāt, Punjab
- Aziz Bhatti Shaheed Teaching Hospital — Gujrāt, Punjab, Pakistan (Recruiting)
Study contacts
- Principal investigator: Wajiha Shahid, phd — Riphah International University
- Study coordinator: Wajiha Shahid, phd
- Email: wajiha.shahid@riphah.edu.pk
- Phone: 03214885079
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.