A clinical trial to study the effect of inward heel in medial knee osteoarthritis with flatfoot by using modified University of California-Berkeley Laboratory (UCBL) orthosis
Phase 2
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2023/09/057706
- Lead Sponsor
- Pandit Deendayal Upadhyaya National Institute for persons with physical disabilities Divyangjan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a)Knee osteoarthritis (K-L grade 1-3)
b)Medial compartment involvement
c)Participants age group > 45 years
d)Pronated foot type (pes planus)
e)OA group able to walk independently
Exclusion Criteria
a)Subjects with functional limitation or
disabilities
b)knee valgus alignment
c)Other hip or knee pathological conditions
d)History of hip, knee or foot surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is to evaluate the following parameters <br/ ><br>The dynamic center of gravity (COG) sway changes in X,Y & Z axis using mobile accelerometer,to evaluate osteoarthritic symptoms including pain, stiffness & physical function using the western Ontario & McMaster Universities questionnaire and <br/ ><br>To evaluate Knee Varus angulation using Femorotibial angle (FTA) through radiological x ray.Timepoint: 3 weeks of adaptation time.
- Secondary Outcome Measures
Name Time Method foot print diagnosis using x ray imaging & to evaluate Talar-first metatarsal angle and Talo-Navicular coverage angle.Timepoint: before & after 3 weeks of adaptation time.