Health Condition 1: M171- Unilateral primary osteoarthritisof knee
Conditions
Interventions
Intervention1: Eccentric exercise + conventional care (ECC group): The ECC group will receive 15 sessions of eccentric knee flexor-extensor and hip extensor-abductor exercises along with 18 sessions o
recommended mobilization with movement, including patellar gliding for knee OA - 6-10 reps/1-3 sets
application of therapeutic pulsed ultrasound at 1-MHz/ 0.8 W/cm/ 5 minutes/ once a day (Use a 5cm2 diameter applicator) under the supervision of the physiotherapist. After that, during the 4th 18th
eccentric knee extensor exercise on a thigh extension machine
eccentric hip extensor exercise on a Roman chair set 30 relative to the floor
and eccentric hip abductor exercise using a cable machine in the gymnasium
weight will be distributed according to the participants tolerance level and conditions - 10 reps/1-3 sets. Finally, cool down for 5 minutes.
Intervention2: Isometric exercise + conventional care (IS
Sponsors
Kazi Md Azman Hossain
Eligibility
Inclusion criteria
Inclusion criteria: Individuals will be included in this trial if (1) ages 45 70 for both men and women, (2) the presence of knee OA for at least six months following American College of Rheumatology criteria, (3) able to walk without the use of any aids and able to flex the knee beyond 90 degrees, (4) anterior-posterior bilateral standing radiograph presents Kellgren and Lawrence Grade II/III knee OA, and (5) absence any unusual cardiac response during the six-minute walk test.
Exclusion criteria
Exclusion criteria: Individuals will be excluded if (1) knee surgery has been performed in the previous twelve months, (2) lumbar radiculopathy, vascular claudication, severe anterior-sided knee pain resulting from patella-femoral syndrome or chondromalacia, as well as further neurological, muscular, or joint conditions that could impair the function of the lower limbs, (3) visible malformation of the knee, either varus or valgus, (4) Received hyaluronic acid or corticosteroid injections within three months of study enrollment, (5) pregnancy, and (6) BMI over 30
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain (Numeric Pain Rating Scale), Pressure Pain Threshold (Algometer), Muscle strength (Sphygmomanometer), Range of Motion (Goniometer)Timepoint: At baseline, after 6 weeks and 24 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional ability (WOMAC), Walking ability (6MWT)Timepoint: 10 months | — |
Countries
Bangladesh
Contacts
Public ContactAbid Hasan Khan
Jashore University of Science and Technology (JUST), Jashore
Outcome results
None listed