A Clinical trial to compare the final effects after 3 months between two groups of patients with Axial Spondyloarthritis,of which one group will be undergone Supervised Rehabilitation Programme,another group will be undergone therapeutic Home Exercise Progamme.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Axial Spondyloarthritis
- Registration Number
- CTRI/2018/01/011127
- Lead Sponsor
- Dr ARUPRATAN GHOSH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 63
Inclusion Criteria
Patients fulfilling ASAS critria for Axial Spondyloarthritis.
Exclusion Criteria
1.Active non-inflammamatory Spinal Disease.
2.Pregnancy.
3.Hip and Knee deformity.
4.Past history of Orthopedic Surgery on Axial Skeleton and peripheral joints.
5.Psychiatric illness.
6.Hypertension.
7.Diabetes.
8.Past or present history of Tuberculosis.
9.patients on Biologic drugs for any ailment since last 1 year.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Physical function. <br/ ><br>2.Spinal pain. <br/ ><br>3.Spinal Mobility. <br/ ><br>4.Patient Global assessment. <br/ ><br>5.Stiffness. <br/ ><br>6.Fatigue. <br/ ><br>7.Disease activity.Timepoint: 1.Physical function at 3 months. <br/ ><br>2.Spinal pain at 3 months. <br/ ><br>3.Spinal Mobility at 3 months. <br/ ><br>4.Patient Global assessment at 3 months. <br/ ><br>5.Stiffness at 3 months. <br/ ><br>6.Fatigue at 3 months. <br/ ><br>7.Disease activity at 3 months.
- Secondary Outcome Measures
Name Time Method not applicableTimepoint: not applicable