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Effect of two different electrical stimulation on quadriceps for pain and function in patients after Total Knee Replacement

Not Applicable
Conditions
Health Condition 1: null- Unilateral Total Knee Replacement
Registration Number
CTRI/2018/05/013611
Lead Sponsor
Sancheti Institute College of Physiotherapy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients who have undergone unilateral Total Knee Arthroplasty secondary to severe knee osteoarthritis.

Exclusion Criteria

1.Post traumatic TKA

2.Revision TKA

3.Significant neurological impairments

4.Any lower limb deformity

5.Dermatological conditions and impaired sensation affecting thethigh

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.PAIN:Quadruple visual analogue scale(QVAS) <br/ ><br>2.Range of motion-Supine knee flexion and extension <br/ ><br>3.Quadriceps strength- quadriceps Extension lag <br/ ><br>4.Functional mobility measure-Timed up and go test <br/ ><br>5.Functional disability scale-Knee Outcome Survey Activities of Daily living Scale(KOS-ADL) <br/ ><br>Timepoint: -Post-operative day 2(prior to commencement of intervention) <br/ ><br>-Post-opertive day 5 (after completion of the intervention)
Secondary Outcome Measures
NameTimeMethod
1.PAIN:Quadruple visual analogue scale(QVAS) <br/ ><br>2.Range of motion-Supine knee flexion and extension <br/ ><br>3.Quadriceps strength- quadriceps Extension lag <br/ ><br>4.Functional mobility measure-Timed up and go test <br/ ><br>5.Functional disability scale-Knee Outcome Survey Activities of Daily living Scale(KOS-ADL) <br/ ><br>Timepoint: -Post-operative day 2(prior to commencement of intervention) <br/ ><br>-Post-operative day 5 (after completion of the intervention)
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