Effectiveness of Dry Needlingand Fascial Manipulation OnChronic Knee OA Patients withCentral Sensitization: A singlegroup pre post design
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 28
- Locations
- 1
- Primary Endpoint
- •WOMAC Scale
Study Overview
Brief Summary
After submitting informed consent, criteria for inclusion and exclusion are checked, patients who meet inclusion criteria, pre intervention outcome measure assessment will be measured using WOMAC, NPRS, Range of Motion, PPT, TAMPA Scale, Pain- self efficacy scale and CSI will be measured as screening tool. After assessing knee OA with central sensitization dry needling and fascial manipulation will be given to subjects once a week for four weeks. Post treatment assessment will be done after 4 weeks, follow up will be taken on 3 month and 6 months.
Study Design
- Study Type
- Interventional
- Allocation
- Not Applicable
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 40.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Knee osteoarthritis as defined by the American College of Rheumatology (knee discomfort and at least three of the following: 50 years or older, bony enlargement, crepitus on active motion, bony soreness, 30 minutes of morning stiffness, and no perceptible warmth of synovial) Based on radiological findings, Kellgren and Lawrence grade2,3, and 4 The ideal CSI score is under 40.
Exclusion Criteria
- •Knee arthroplasty Intra-articular steroid injection and/or oral steroid treatment within the last six months Total Meniscectomy Neurological deficits in the lower limb Cancer, rheumatoid arthritis, severe cognitive deficit Lymph edema, peripheral vascular disease Infection and allergy present in lower limb [ Skin Ulcer].
Outcomes
Primary Outcomes
•WOMAC Scale
Time Frame: Pre intervention(1st day) | Post intervention(4th week) | Follow up(3rd month 6th month)
Secondary Outcomes
- TAMPA scale of Kinesio phobia(NPRS)
