A comparative study of SNAG versus Mulligan’s Bent Leg Raise technique along with traditional physiotherapy in patients with non-specific mechanical low back pain
- Conditions
- Acquired deformity of musculoskeletal system, unspecified,
- Registration Number
- CTRI/2025/06/088145
- Lead Sponsor
- Rohan Bhardwaj
- Brief Summary
This randomized comparative experimental study aims to evaluate and compare the effectiveness of two manual therapy techniques Sustained Natural Apophyseal Glide SNAG and Mulligans Bent Leg Raise BLR when used alongside traditional physiotherapy in the treatment of non specific mechanical low back pain NSMLBP. A total of 58 participants aged 18 to 60 years will be randomly assigned into two equal groups. Group A will receive SNAG with traditional physiotherapy while Group B will receive Mulligans BLR technique with traditional physiotherapy. Both groups will undergo treatment three times per week for four weeks. Outcome measures including pain measured by Numeric Pain Rating Scale NPRS functional disability assessed by Oswestry Disability Index ODI lumbar range of motion measured by goniometry and the Straight Leg Raise SLR test will be assessed at baseline mid intervention second week and post intervention fourth week. The study seeks to determine which manual therapy approach provides superior clinical outcomes in pain relief mobility and functional improvement in patients with NSMLBP.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 58
Both males and females Patients with non-specific Mechanical low back pain.
- 1.Fracture 2.Tumors 3.Infection 4.Inflammatory diseases 5.Individuals with neurological deficits 6.Chronic pathological pain 7.Conditions that could affect their ability to participate in the exercises.
- 8.Patients who had undergone previous surgical interventions for low back pain.
- 9.Any contraindication to physiotherapy & manual therapy.
- 10.Those who were currently receiving other forms of treatment for low back pain that could confound the results.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method NPRS -Numeric Pain Rating Scale Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day) ODI-Oswestry Disability Index Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day) GONIOMETER Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day) Straight Leg Raise (SLR) test Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Shri Mahant Indiresh Hospital
🇮🇳Dehradun, UTTARANCHAL, India
Shri Mahant Indiresh Hospital🇮🇳Dehradun, UTTARANCHAL, IndiaDr Rohan BhardwajPrincipal investigator9579939682bhardwajrohan21@gmail.com