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TO CHECK THE EFFECT BLOOD FLOW RESTRICTION EXERCISE AND PROGRESSIVE RESISTED EXERCISE ON PAIN PHYSICAL FUNCTION AND MUSCLE STRENGTH IN SUBJECTS WITH OSTEOARTHRITIS OF KNEE

Phase 2/3
Not yet recruiting
Conditions
Osteoarthritis of knee, unspecified,
Registration Number
CTRI/2022/01/039083
Lead Sponsor
Parul Institute of Physiotherapy
Brief Summary

To compare effectiveness of blood flow restriction and progressive resisted exercise on pain physical function and muscle strength in subjects with osteoarthritis of knee.To determine the effect of BFR on pain in subjects with osteoarthritis of knee.

To determine the effect of  BFR on physical function in subjects with osteoarthritis of knee.

To determine the effect of  BFR on muscle strength in subjects with osteoarthritis of knee.

To determine the effect of PRE on pain in subjects with osteoarthritis of knee.

To determine the effect of PRE on physical function in subjects with osteoarthritis of knee.

To determine the effect of PRE on muscle strength in subjects with osteoarthritis of knee.

To compare the effectiveness of BFR and PRE on pain in subject with osteoarthritis of knee.

To compare the effectiveness of BFR and PRE on physical function in subject with osteoarthritis of knee.

To compare the effectiveness of BFR and PRE on muscle strength in subject with osteoarthritis of knee

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria
  • 1.Subjects with Mild to moderate knee pain 2.Participants will be given a written consent form.
  • 3.Knee OA of one or both knees with grade 1 or 2 (Kellgren and Lawrence classification system) based on plain x-rays.
Exclusion Criteria
  • 1.History of peripheral vascular disease 2.History of neurological disease with affected the gait 3.History of undergone surgery or any invasive procedure on knee in previous 6 months.
  • 4.History of lower extremity infection.
  • 5.Subject who is taking medications known to increase the clotting risk.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1 RM is 1 repetition maximum. It is used to check the strength of muscle.In which how much person can lift the weight according we will measure the strength of muscle.It will be measured before 1st day of intervention and after 4 week of intervention.
Secondary Outcome Measures
NameTimeMethod
WOMAC SCORE: It is evaluate the osteoarthritis of knee joint. it is self administreted intrument.
VAS : It is subjective measure for pain.score will be recorded by making handwritten mark on 10 cm line that represents continuum between no pain and worst painVAS will be measure before 1st intervention and after 4 week of intervention

Trial Locations

Locations (1)

Parul Sevashram Hospital

🇮🇳

Vadodara, GUJARAT, India

Parul Sevashram Hospital
🇮🇳Vadodara, GUJARAT, India
Dr Drashti Jani
Principal investigator
8488832389
janidrashti333@gmail.com

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