Overview
This study is a randomised control trial and the purpose of this study is to determine the effects Post facilitation stretch versus reciprocal inhibition on pain, lumbar range of motion, apparent leg length discrepancy and lumbar lordotic angle in Quadratus Lumborum Syndrome.
Description
The purpose of this study is to determine the difference between Post facilitation, stretch versus reciprocal inhibition on pain, lumbar range of motion, apparent leg length discrepancy and lumber lordotic angle in Quadratus Lumborum Syndrome.
The individual of Age 18-35 years among both genders, who experiences pain of 3 ≤ on NPRS from at least 3 months and whose pain decreases on supine lying; along with any two of the following findings positive of quadratus lumborum on physical examination i.e., Taut bands, Local tenderness, Patient's pain recognition, Pain referral to greater trochanter, Local twitch response & Jump sign will be recruited in the study as patients of Quadratus lumborum syndrome.
Pain levels will be assessed using the Numeric Pain Rating Scale (NPRS). Inclinometer will be used for measuring lumber ranges. To assess apparent leg length discrepancy measuring tape will be used. The lumbar lordotic angle will be measured using 60 cm flexible ruler. Participants of interest would be approached and explained about the research. Informed written consent will be taken. It is a non-blinded study and randomization will be done through sealed envelope. Both groups will receive conventional intervention. Additionally, Group A will receive quadratus lumborum post facilitation stretches while Group B will receive Reciprocal inhibition. Baseline and post intervention scores would be recorded for both groups.
Eligibility
Inclusion Criteria:
- Age 18-35 years
- Both genders
- Having pain of ≤ 8 on NPRS from at least 3 months
- Pain decreases on supine lying
- Any two of the following findings positive of unilateral quadratus lumborum on
physical examination:
- Taut bands
- Local tenderness
- Patient's pain recognition
- Pain referral to greater trochanter
- Local twitch response
Exclusion criteria:
- Painful isometric muscle testing of hip flexors, abductors, adductors, and extensors
- Previous surgery of lower limb
- Centralization/peripheralization
- Lower back trauma
- Positive SLR
- Radiculopathy
- Fracture/surgery of pelvic and/or hip region
- Diagnosed fibromyalgia or other rheumatic diseases.
- Lactating women
- Intrauterine device
- Pregnant women
- Use of psychiatric medications