Skip to main content
Clinical Trials/CTRI/2024/11/076800
CTRI/2024/11/076800Not yet recruitingPhase 3

Effect of foot-ankle strengthening exercises on pain, range of motion and functional performance in patients with symptomatic knee osteoarthritis.

Muskan Jain1 site in 1 country50 target enrollmentStarted: November 25, 2024Last updated:

Trial Snapshot

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Visual Analogue Scale (VAS)

Study Overview

Brief Summary

PROCEDURE  The eligibility criteria of the candidate will be taken from the basis of inclusion criteria.

50 samples will be categorized into two groups with 25 individuals in each group and will be studied for 4 weeks.

Group- A: Foot-Ankle strengthening exercises + conventional physiotherapy.

Group- B: conventional physiotherapy.

Group-A

Foot-Ankle strengthening exercises: involving isolated strengthening of extrinsic and intrinsic foot- ankle muscles, and of strengthening and functional training of extrinsic and intrinsic foot- ankle muscles.

Conventional physiotherapy: Ultrasound Therapy, knee strengthening exercises and stretching (Hamstrings, calf and hip flexors).

Group- B

Conventional physiotherapy: Ultrasound Therapy, knee strengthening exercises and stretching (Hamstrings, calf and hip flexors).

Treatment would be done under supervision with consent.

The total duration of the treatment program will be of 4 weeks. Foot-Ankle strengthening exercises and conventional exercises will be performed twice daily, with 10 repetitions in 3 sets in a session with 10-20 seconds hold, 1 minute rest time between sets. Ultrasound therapy will be given as 4 sessions in a week, each session will be of 5 minutes.

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) will be given to patients before & after the treatment, & will be used as a primary outcome measure. Pain will be assessed by using Visual Analogue Scale (VAS) & Range of Motion of the joint will be assessed by Goniometer.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
40.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Case of symptomatic Osteoarthritis Knee Kellgren_Lawrence grade-1,2,3 Knee pain in range of 30mm-70mm(3-7) on VAS.

Exclusion Criteria

  • Traumatic Knee Injury/ fracture Having received steroid and hyaluronic acid intra-articular knee injections in the previous 3 and 6 months, respectively.
  • History of knee, ankle or hip surgery in the last 2 years.
  • Neurological illness or deficit Inflammatory arthritis (e.g., rheumatoid arthritis).
  • Asymptomatic Knee Osteoarthritis in one or both knees.
  • Open Wounds / Ulcerations Skin infections.

Outcomes

Primary Outcomes

Visual Analogue Scale (VAS)

Time Frame: 4 weeks

Goniometer

Time Frame: 4 weeks

Western Ontario and McMaster Universities Arthritis Index (WOMAC)

Time Frame: 4 weeks

Secondary Outcomes

  • Visual Analogue Scale (VAS)(2 weeks)

Investigators

Sponsor
Muskan Jain
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Muskan Jain

Mahatma Gandhi University of Medical Sciences and Technology, Jaipur

Study Sites (1)

Loading locations...

Similar Trials

Effectiveness of Foot-Ankle strengthening... | Clinical Trial