Comparison of effects of mobilization with movement at Sacroiliac joint with and without Postero-Anterior Glide at L5-S1 in patients with Sacroiliac joint dysfunctio
- Conditions
- sacroiliac joint dysfunction.
- Registration Number
- IRCT20200527047582N1
- Lead Sponsor
- Ghurki trust and teaching hospital, Lahore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 26
Patients who had an acute unilateral or bilateral SIJ syndrome during the past 6 weeks.
Those in whom the level of pain over the previous 24 h increased
Patients having no manipulative treatment within the past month.
Pain and tenderness at SIJ
FABER, compression, distraction, and Gaenslen's. provocation tests POSITIVE
Previous spinal manipulative treatment
Having pain and discomfort in the lumbar spine
Destructive lesions of the spine, ribs and pelvis
cauda equina syndrome
Patients having gross instability or active infection
Pregnancy, Spondylolysthesis, and previous back surgery.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: before intervention, after intervention , after 2 weeks and after one month. Method of measurement: Numeric pain rating scale (NPRS): NPRS is anchored by terms describing pain severity extremes. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. no pain”) to '10' representing the other pain extreme (e.g. pain as bad as you can imagine” or worst pain imaginable”).
- Secondary Outcome Measures
Name Time Method Disability. Timepoint: Subjects will be reassessed by researcher immediately after treatment, after 2 weeks and after one month.Treatment sessions (3 session a week) will be given to the subjects. Method of measurement: Oswestry Disability Questionnaire (ODQ):It is a functional index designed to determine the symptoms and limitations that patient experiences while performing daily activities. This scale consists of 10 items in the form of activities of daily living with each item scoring from 0 to 5 where 0 is no difficulty in performing that activity and 5 is inability to do that activity. This will used for assessment of the associated disability.