The study was about a root cause of Primary Osteoarthritis Lumbar Spine producing disabilities in sitting, climbing and walking etc. In advance stage the person is bereft of his/her personal physical activities. The prevalent treatment is temporary and dis-satisfactory. A new treatment was designed and a trial was conducted on 154 patients (100 in the trial group, 50 in the control group) for a duration of six months.
The study was focused on establishing the cause, pathogenesis and treatment of painful Lumbar Spine disease (Primary Osteoarthritis Lumbar Spine = OA Lumbar Spine) at present the exact cause and treatment are not known. It was aimed to find out to latter through a hypothesis by designing a treatment and testing it with a clinical trial. This established that the deficient full extension of the spinal joints (intervertebral joints between the adjacent vertebrae from T12 to S1) producing contracture in their capsules in front, was the cause and the correction (Contracture Correction Therapy = CCT) was the cure of the disease. The correction was carried out by intermittent and sustained extension of the lumbar spin through three designed body postures.
Study Type
OBSERVATIONAL
Enrollment
154
Arogya Sadan Nursing Home
Bhind, Madhya Pradesh, India
Sai Baba Dharmarth Chikitsalaya
Gwalior, Madhya Pradesh, India
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The Western Ontario and McMaster Universities Arthritis Index (WOMAC)
It is a self-administered questionnaire consisting of 24 items divided into 3 subscales
Time frame: Change from baseline The Western Ontario and McMaster Universities Arthritis Index Osteoarthritis score at 6, 12, 24 weeks
Oswestry Disability Index
Patient-completed questionnaire which gives a subjective percentage score of level of function (disability) in activities of daily living in those rehabilitating from low back pain.
Time frame: Change from baseline Oswestry Disability Index score at 6, 12, 24 weeks
EuroQol Visual Analogue Scale score
The EQ-VAS is a vertical visual analogue scale that takes values between 100 (best imaginable health) and 0 (worst imaginable health), on which patients provide a global assessment of their health.
Time frame: Change from baseline EuroQol Visual Analogue Scale score at 6, 12, 24 weeks
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