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Clinical Trials/CTRI/2025/01/079514
CTRI/2025/01/079514
Not yet recruiting
Phase 2

Effect of valgus control instruction exercises versus conventional treatment on pain, strength and function in patients with patellofemoral pain syndrome -An experimental study

MAEERs Physiotherapy College1 site in 1 country46 target enrollmentStarted: February 1, 2025Last updated:

Overview

Phase
Phase 2
Status
Not yet recruiting
Sponsor
MAEERs Physiotherapy College
Enrollment
46
Locations
1
Primary Endpoint
Pain (visual analogue scale), strength (hand held dynamometer)

Overview

Brief Summary

Patellofemoral pain syndrome (PFPS) is a prevalent knee condition characterized by pain around or behind the patella, typically worsened by activities like squatting, running, or stair climbing that place stress on the knee. It affects a broad range of people, especially young, active individuals and athletes, with a higher prevalence in females due to factors such as greater quadriceps angle (Q angle) and dynamic valgus. PFPS is often caused by a misalignment in patellar tracking during knee movement, with biomechanical issues like weak lower extremity muscles, tightness in structures around the knee, and foot overpronation contributing to the condition.

Recent studies explore the impact of valgus control instruction (VCI) exercises, which aim to correct knee valgus by re-educating motor control. Exercise instructions can be categorized into internal focus (IF), which directs attention to body movements, and external focus (EF), which focuses on movement outcomes. EF instructions are thought to better facilitate motor learning by encouraging instinctive responses. VCI exercises show promise in improving knee alignment, particularly in comparison to conventional treatments, offering a potential benefit in managing PFPS.

A visual analog scale will be used to evaluate anterior knee pain in participants who meet the inclusion criteria. A dynamometer will be used to measure quadriceps, hip abductors, and external rotators strength, and an anterior knee pain scale will be used to evaluate function. Using the simple random sampling technique, the participants who meet the inclusion requirements will be divided into two groups. For six weeks, one group will receive traditional treatment three times a week, while the other group will receive exercises involving valgus control teaching three times a week.

All the three outcomes will be assessed after 6 weeks of intervention. Data will be collected and analyzed.

Study Design

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

Eligibility Criteria

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

Inclusion Criteria

  • Anterior knee pain patients diagnosed by Orthopedic The clinical practice guideline for PFPS by The American Physical Therapy Association diagnostic criteria: Presence of retro patellar or peripatellar pain Reproduction of retro patellar or peripatellar pain during squatting, or other functional activities loading the PFJ in a flexed position.

Exclusion Criteria

  • Previous surgery in lower limb Any other diagnosed knee and hip conditions Patellar instability/ subluxation Low back pain referring pain to knee.

Outcomes

Primary Outcomes

Pain (visual analogue scale), strength (hand held dynamometer)

Time Frame: pre and post intervention 6 weeks

Secondary Outcomes

  • function (anterior knee pain scale)(pre and post intervention 6 weeks)

Investigators

Sponsor
MAEERs Physiotherapy College
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Rasika Sawarkar

MAEERS Physiotherapy College Talegaon Dabhade

Study Sites (1)

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